Title of Invention	OXIME COMPOUNDS
Abstract	Oxime compounds of formula (1) wherein Rl, R2, and R3 are independently halogen, C1-C3 alkyl, C1-C3 halo- lalkyl, C1-C3 alkoxy, C1-C3 haloalkoxy, nitro, or cyano; R4 is 3, 3-dihalogeno-2- propenyl; a is an integer of 0 to 2; Y is oxygen, sulfur, or NH; Z is oxygen, sulfur, or NR5 wherein R5 is hydrogen, acetyl, or C1-C3 alkyl; and X is of formula (2) insecticidal/acaricidal agents containing them as active ingredients; and intermediates for their production.

Title of Invention

OXIME COMPOUNDS

Abstract

Oxime compounds of formula (1) wherein Rl, R2, and R3 are independently halogen, C1-C3 alkyl, C1-C3 halo- lalkyl, C1-C3 alkoxy, C1-C3 haloalkoxy, nitro, or cyano; R4 is 3, 3-dihalogeno-2- propenyl; a is an integer of 0 to 2; Y is oxygen, sulfur, or NH; Z is oxygen, sulfur, or NR5 wherein R5 is hydrogen, acetyl, or C1-C3 alkyl; and X is of formula (2) insecticidal/acaricidal agents containing them as active ingredients; and intermediates for their production.

Full Text	DESCRIPTION OXIME COMPOUNDS, THEIR USE, AND INTERMEDIATES FOR THEIR PRODUCTION Technical Field The present invention relates to oxime compounds, their use, and intermediates for their production. Background Art As disclosed, for example, in JP-A 61-72733 and JP-A 61-260054, it is well known that certain types of oxime compounds can be used as the active ingredients of insecticides. These compounds are, however, not necessarily satisfactory for the active ingredients of insecticidal/acaricidal agents in view of their insecticidal activity. Disclosure of Invention Under these circumstances, the present inventors have extensively studied to find out compounds with excellent insecticidal/acaricidal activity. As a result, they have found that oxime compounds of formula (1) as depicted below have excellent insecticidal/acaricidal activity, thereby completing the present invention. Thus, the present invention provides oxime compounds of formula (1) (hereinafter referred to as the present compound(s)) wherein: R1 R2 and R3 are independently halogen, C1-C3 alkyl, C1-C3 naioaiKyi, C1-C3 alkoxy, C1-C3 haloalkoxy, nitro, or cyano; R4 is 3,3-dihalogeno-2-propenyl; a is an integer of 0 to 2; Y is oxygen, sulfur, or NH; Z is oxygen, sulfur, or NR5 wherein R5 is hydrogen, acetyl, or Cj-Cg alkyl; X is X1 or X2 of formula (2) wherein: R6 is hydrogen, C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, Cg-Cg haloalkenyl, C3-C6 alkynyl, C3-C6 haloalkynyl, or triphenyl-methyl, or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C5-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or Cfi-Cg cycloalkenylalkyl optionally substituted with Ci-C4 alkyl on the ring thereof, or Ci-Cg alkyl substituted with cyano, nitro, (C1-C4 alkoxy)-carbonyl, C1-C4 alkylthio, or C1-C4 alkoxy, or T1-l, T1-2, T1-3, T1-4, T1-5, T1-6, or T1-7 of formula (3) (R10')b's are zero to five identical or different substi-tuents selected from halogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 halo-alkynyl, C1-C6 alkoxy, C1-C3 haloalkoxy, C3-C6 alkenyloxy, C2-C6 haloalkenyloxy, C2-C6 alkynyloxy, C3-C6 haloalkynyloxy, (C1-C5 alkoxy)carbonyl, cyano, or nitro; R11, R12, R13, and R14 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl; D is -CH= or nitrogen; J is oxygen or sulfur; b is an integer of 0 to 5; d is an integer of 1 to 3; e is an integer of 0 to 3; f is an integer of 2 to 4; R15 is C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, or C2-C6 cycloalkyl, or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C4 alkoxy, or C1-C3 haloalkoxy; and R16 and R42 are independently C1-C3 alkyl, C2-C6 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C3-C6 haloalkynyl, or C2-C6 cycloalkyl, or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C4 alkoxy, or C1-C3 haloalkoxy, or benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C4 alkoxy, or C1-C3 haloalkoxy on the ring thereof; R7 is hydrogen, C1-C3 alkyl, C1-C3 haloalkyl, C2-C6 cycloalkyl, cyano, cyano C1-C3 alkyl, (C1-C4 alkoxy)carbonyl, or (C1-C4 alkoxy)-carbonyl(Ci-C3)alkyl, or phenyl optionally substituted with halogen, Ci-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy, or benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof; R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C2-C10 alkoxyalkyl, C2-C10 alkylthioalkyl, or naphthyl, or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C2-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 on the ring thereof, or T2-l or T2-2 of formula (4) wherein: (R17)b's are zero to five identical or different substi-tuents selected from halogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C1-C3 alkoxy, C1-C3 haloalkoxy, C2-C6 alkenyloxy, C2-C6 haloalkenyloxy, C2-C6 alkynyloxy, C2-C6 haloalkynyloxy, C1-C3 alkylthio, C1-C3 haloalkylthio, C1-C3 alkylsulfinyl, C1-C2 alkylsvdfonyl, C1-C3 haloalkylsulfinyl, C1-C2 haloalkylsulfonyl, C1-C3 hydroxyalkyl, C2-C4 alkoxyalkyl, C2-C4 alkylthioalkyl, dimethylamino, acetamido, acetyl, formyl, carboxyl, (C1-C3 alkyl)aminocarbonyl, [di(C1-C2 alkyl)amino]carbonyl, (C1-C3 alkoxy)carbonyl, C3-C6 cycloalkyl, C2-C6 cycloalkenyl, C2-C6 cycloalkyloxy, C2-C6 cycloalkenyloxy, pentafluorosulfanyl (FgS), cyano, or nitro, or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy, or phenoxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy, or benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, or when b is 2 to 5, two adjacent R17's are combined together at their ends to form trimethylene or tetramethyl- ene, or when b is 2 to 5, two adjacent R^^'s are combined together at their ends to form methylenedioxy optionally substituted with halogen or C1-C3 alkyl, or when b is 2 to 5, two adjacent R17's are combined together at their ends to form ethylenedioxy optionally substituted with halogen or C1-C3 alkyl; D is -CH= or nitrogen; R11 and R12 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl; b is an integer of 0 to 5; and d is an integer of 1 to 3; or a heterocyclic group, exclusive of pyridine ring, which heterocyclic group may be optionally substituted with one to three identical or different (R18)g s, wherein: R18 is halogen, C1-C3 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C1-C3 alkoxy, C1-C3 haloalkoxy, C2-C6 alkenyloxy, C3-C6 haloalkenyloxy, C2-C6 alkynyloxy, C3-C6 haloalkynyloxy, C1-C3 alkylthio, C1-C3 haloalkylthio, C1-C2 alkylsulfinyl, C1-C3 alkylsulfonyl, C1-C2 haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3 hydroxyalkyl, C2-C4 alkoxyalkyl, C2-C4 alkylthioalkyl, cyano, or nitro, or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy; and g is an integer of 1 to 3; or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring; A1 is A1-l, A1-2. A1-3, A1-4, A1-5, A1-6, A1-7, A1-8, A1-9, A1-10, methyl; R22 is hydrogen, C1-C3 alkyl, or trifluoromethyl, or when h is 0 and i is 1 in A^-1, R^^ and R^ may be combined together at their ends to form trimethylene, tetra-methylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl, or when h is 0 and j is 1, in A1-2, A1-3, A1-4, A1-5, or A1-6, R22 and R7 may be combined together at their ends to form trimethylene, tetramethylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl; h is an integer of 0 or 1; i is an integer of 1 to 6; j is an integer of 1 to 3; k is an integer of 2 to 8; m is an integer of 1 to 3; n is an integer of 1 to 3; p is an integer of 0 or 1; q is an integer of 0 or 1; r is an integer of 2 to 4; s is an integer of 2 to 4; t is an integer of 0 to 3; u is an integer of 0 to 3; V is an integer of 1 to 4; w is an integer of 1 to 4; X is an integer of 1 to 4; Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2; Q2 is oxygen, S(0)z, or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2; E is C5-C6 cycloalkylene; U1 is U1 of formula (6) -G1-W-wherein: W is an optionally substituted benzene ring or an optionally substituted heterocyclic ring; G1 is G1-l or G1-2 of formula (7) Q2 is oxygen, S(0)z, or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2; R35 R36 R37 and R38 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl; al is an integer of 0 to 4; bl is an integer of 1 to 3; and dl is an integer of 0 to 2; and G2 is oxygen, 8(0)a1, or NR39 wherein R39 is h is an integer of 0 or 1; j is an integer of 1 to 3; m is an integer of 1 to 3; n is an integer of 1 to 3; p is an integer of 0 or 1; t is an integer of 0 to 3; u is an integer of 0 to 3; fl is an integer of 1 to 3; Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2; E is C2-C6 cycloalkylene; U3 is U3-l, U3.2, or U3-3 of formula (10) wherein: R35 and R36 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl; (R40)gi's are zero to four identical or different substituents selected from halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy; R and V are independently -CH= or nitrogen; gl is an integer of 0 to 4; wherein: R35 and R36 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl; (R40)gi's are zero to four identical or different substituents selected from halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy; R and V are independently -CH= or nitrogen; gl is an integer of 0 to 4; hi is an integer of 1 to 3; il is an integer of 2 or 3; Q2 is oxygen, S(0)„ or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2; and Q3 is oxygen, 8(0)e,1, or NR39 wherein R39 is hydrogen or C1-C3 alkyl, and el is an integer of 0 to 2; and insecticidal/acaricidal agents containing them as active ingredients. In particular, the oxime compounds of formula (1) wherein X is X1 and R6 is hydrogen are useful both as the active ingredients of insecticidal/- acaricidal agents and as the intermediates for the production of these active ingredient compounds. The present invention further provides hydroxylamine compounds of formula (12) wherein R1 R2, R3, R4 a, Y, Z, and A2 are as defined above, and salts thereof (e.g., inorganic acid salts such as hydrochlorides, sulfates, and nitrates). The present invention further provides compounds of formula (13) wherein R2 R3 R7 R19, R20, and j are as defined above, and R41 is 3,3-di-chloro-2-propenyl, 3,3-dibromo-2-propenyl, or 3-bromo-3-chloro-2-propenyl, which are useful as the intermediates for the production of the present compounds. The present invention further provides compounds of formula (14) wherein R2, R3 R7 R19 R20 R29 R30 R41 j, and v are as defined above, which are useful as the intermediates for the production of the present compounds. The present invention further provides phenol compounds of formula (50) wherein R1 R2, R3, a, X, and Z are as defined above, with the proviso that when X is X1 R6 is not hydrogen, which are useful as the intermediates for the production of the present compounds. ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, 1-ethylpropyl, n-hexyl, isohexyl, 2-ethyl-butyl, 1-methylpentyl, 1-ethylbutyl, 3-methylpentyl, 1,3-dimethylbutyl, n-heptyl, 1-ethyl-l-methylbutyl, n-octyl, and 1-methylheptyl. The C1-C6 alkyl represented by R7 R10 R15 R16 R42 R17 or R18 may include, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, 1-ethylpropyl, n-hexyl, isohexyl, 2-ethylbutyl, 1-methylpentyl, 1-ethylbutyl, 3-methylpentyl, and 1,3-dimethylbutyl. The C1-C11 alkyl represented by R8 or R9 may include, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, 1-ethylpropyl, n-hexyl, isohexyl, 2-ethylbutyl, 1-methylpentyl, 1-ethylbutyl, 3-methylpentyl, 1,3-dimethyl-butyl, n-heptyl, l-ethyl-l-methylbutyl, n-octyl, 1-methylheptyl, n-nonyl, n-decyl, and n-undecyl. The C1-C4 alkyl represented by R40 may include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, and tert-butyl. The C1-C3 haloalkyl represented by R1 R2, R3 R7 R10 R15 R17 R18, or R40 may include, for example, trifluoromethyl, difluoromethyl, bromo-difluoromethyl, 1-fluoroethyl, 1-chloroethyl, 1-bromoethyl, perfluoroethyl, 2-bromo-l,l,2,2-tetrafluoroethyl, 1,1,2,2-tetrafluoroethyl, 2-chloro-l,l,2-tri-fluoroethyl, 2-bromo-l,l,2-trifluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloro-ethyl, 2,2,2-tribromoethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodo-ethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3, 3-hexafluoropropyl, l,l,l,3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloro-propyl, 2-bromopropyl, 2-iodopropyl, and 2,3-dibromopropyl The C2-C6 haloalkyl represented by R6, R16, or R41 may include, for example, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoropropyl, 1,1,1, 3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bromopropyl, 2-iodopropyl, 2,3-dibromopropyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl, 4-iodobutyl, 3-chloro-2,2-dimethylpropyl, 3-bromo-2,2-dimethylpropyl, 2,2,3, 3,4,4,5,5-octafluoropentyl, 6-chlorohexyl, and 6-bromohexyl The C1-C6 haloalkyl represented by R8 or R9 may include, for example, trifluoromethyl, trichloromethyl, difluoromethyl, bromodifluoromethyl, 2,2, 2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopro-pyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoropropyl, 1,1,1,3,3,3-hexa-fluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bromopropyl, 2-iodopropyl, 2,3-dibromopropyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl, 4-iodobutyl, 3-chloro-2,2-dimethylpropyl, 3-bromo-2,2-dimethylpropyl, 2,2,3,3,4,4,5,5-octafluoropentyl, 6-chlorohexyl, and 6-bromohexyl The C1-C3 alkoxy represented by R1 R2, R3, or R40 may include methoxy, ethoxy, n-propyloxy, and isopropyloxy. The C1-C3 alkoxy represented by R10, R17 and R18 may include, for example, methoxy, ethoxy, n-propyloxy, isopropyloxy, n-butyloxy, isobutyloxy, sec-butyloxy, tert-butyloxy, n-pentyloxy, isopentyloxy, neopentyloxy, tert-pentyloxy, 1-ethylpropyloxy, n-hexyloxy, isohexyloxy, 2-ethylbutyloxy, 1-methylpentyloxy, 1-ethylbutyloxy, 3-methylpentyloxy, and 1,3-diemthyl-butyloxy. The C1-C3 haloalkoxy represented by R1 R2 R3 R10 R17 R18, or R40 may include, for example, trifluoromethoxy, bromodifluoromethoxy, 1-fluoro-ethoxy, 1-chloroethoxy, 1-bromoethoxy, perfluoroethoxy, 2-bromo-l,l,2,2-tetrafluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-chloro-1,1,2-trifluoroethoxy, 2-bromo-l,l,2-trifluoroethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy-ethoxy, 2,2,2-tribromoethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2-dichloroethoxy, 2,2-dibromoethoxy, 3-fluoropropyloxy, 3-chloropropyloxy, 3-bromopropyloxy, 3-iodopropyloxy, 3,3,3-trifluoropropyloxy, 2,2,2,3,3,3-hexafluoropropyloxy, 1,1,1,3,3,3-hexa-fluoro-2-propyloxy, 2-fluoropropyloxy, 2-chloropropyloxy, 2-bromopropyloxy, 2-iodopropyloxy, and 2,3-dibromopropyloxy. The C3-C6 alkenyl represented by R6, R16, or R42 may include, for example, allyl, 2-butenyl, 3-butenyl, l-methyl-2-propenyl, 2-methyl-2- propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, l-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, l-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, l-ethyl-2-propenyl, 2-ethyl-2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, l-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, l-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, l-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, and 4-methyl-4-pentenyl The C2-C6 haloalkenyl represented by R6, R16, or R42 may include, for example, 3-chloro-2-propenyl, 3-bromo-2-propenyl, 2-chloro-2-propenyl, 2-bromo-2-propenyl, 3,3-dichloro-2-propenyl, 3,3-dibromo-2-propenyl, 3,3-di-fluoro-2-propenyl, 2,3-dichloro-2-propenyl, 2,3-dibromo-2-propenyl, 2-chloro-methyl-2-propenyl, 4-chloro-2-butenyl, 3-chloro-4,4,4-trifluoro-2-butenyl, 3-bromo-4,4,4-trifluoro-2-butenyl, 3,4-dichloro-4,4-difluoro-2-butenyl, 3,4,4, 4-tetrafluoro-3-butenyl, 4,4-dichloro-3-butenyl, 4,4-dibromo-3-butenyl, 5,5-dichloro-4-pentenyl, 5,5,-dibromO-4-pentenyl, 6,6-dichloro-5-hexenyl, and 6,6-dibormo-5-hexenyl The C2-C6 alkynyl represented by R®, R^^, or R^^ may include, for example, 2-propynyl, 2-butynyl, 3-butynyl, l-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, l-methyl-2-butynyl, l-methyl-3-butynyl, 2-methyl-3-butynyl, l-ethyl-2-propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, l-ethyl-2-butynyl, l-ethyl-3-butynyl, and 2-ethyl-3-butynyL The C3-C6 haloalkynyl represented by R6, R16, or R42 may include, for example, 3-chloro-2-propynyl, 3-bromo-2-propynyl, 4-chloro-2-butynyl, 4-chloro-3-butynyl, 4-bromo-2-butynyl, 4-bromo-3-butynyl, 5-chloro-4-pen-tynyl, 4-chloro-l-methyl-2-butynyl, 4-chloro-l-methyl-3-butynyl, 4-chloro-2-methyl-3-butynyl, 5-bromo-4-pentynyl, 4-bromo-l-methyl-2-butynyl, 4-bro-mo-l-methyl-3-butynyl, 4-bromo-2-methyl-3-butynyl, 6-chloro-5-hexynyl, and 6-bromo-5-hexynyl The C2-C6 alkenyl R8 R9 R10 R15, R17 or R18 may include, for example, vinyl, 1-propenyl, isopropenyl, 1-butenyl, allyl, 2-butenyl, 3-butenyl, 1-meth-yl-2-propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, l-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, l-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, l-ethyl-2-propenyl, 2-ethyl-2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, l-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, l-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, l-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, and 4-methyl-4-pentenyL The C2-C6 haloalkenyl represented by R8 R9 R10 R17 or R18 may include, for example, 2-chloroethenyl, 2-bromoethenyl, 2,2-dichloroethenyl, 2,2-dibromoethenyl, 3-chloro-2-propenyl, 3-bromo-2-propenyl, 2-chloro-2-pro-penyl, 2-bromo-2-propenyl, 3,3-dichloro-2-propenyl, 3,3-dibromo-2-propenyl, 3,3-difluoro-2-propenyl, 2,3-dichloro-2-propenyl, 2,3-dibromo-2-propenyl, 2-chloromethyl-2-propenyl, 4-chloro-2-butenyl, 3-chloro-4,4,4-trifluoro-2-bu-tenyl, 3-bromo-4,4,4-trifluoro-2-butenyl, 3,4-dichloro-4,4-difluoro-2-butenyl, 3,4,4,4-tetrafluoro-2-butenyl, 4,4-dichloro-3-butenyl, 4,4-dibromo-3-butenyl, 5,5-dichloro-4-pentenyl, 5,5-dibromo-4-pentenyl, 6,6-dichloro-5-hexenyl, and 6,6-dibromo-5-hexenyL The C2-C6 alkynyl represented by R8 ,R9 R10 R17 or R18 may include, for example, ethynyl, 1-propynyl, 1-butynyl, 2-propynyl, 2-butynyl, 3-butynyl, l-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, l-methyl-2-butynyl, l-methyl-3-butynyl, 2-methyl-3-butynyl, l-ethyl-2-propynyl, 2-hexynyl, ^ 3-hexynyl, 4-hexynyl, 5-hexynyl, l-ethyl-2-butynyl, l-ethyl-3-butynyl, and 2-methyl-3-butynyl. The C2-C6 haloalkynyl represented by R8 ,R9 R10, R17 or R18 may include, for example, 2-chloroethynyl, 2-bromoethynyl, 3-chloro-2-propynyl, 3-bromo-2-propynyl, 4-chloro-2-butynyl, 4-chloro-3-butynyl, 4-bromo-2-buty-nyl, 4-bromo-3-butynyl, 5-chloro-4-pentynyl, 4-chloro-l-methyl-2-butynyl, 4-chloro-l-methyl-3-butynyl, 4-chloro-2-methyl-3-butynyl, 5-bromo-4-pen-tynyl, 4-bromo-l-methyl-2-butynyl, 4-bromo-l-methyl-3-butynyl, 4-bromo-2-methyl-3-butynyl, 6-chloro-5-hexynyl, and 6-bromo-5-hexynyL The C2-C6 cycloalkyl represented by R7 R15 R16 R17', or R42 may include cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl. The C2-C10 alkoxyalkyl represented by R8 or R9 may include, for example, methoxymethyl, ethoxymethyl, n-propyloxymethyl, isopropyl-oxymethyl, 2-methoxyethyl, 1-methoxyethyl, 2-ethoxyethyl, 1-ethoxyethyl, 3-methoxypropyl, 2-methoxypropyl, l-methoxyp)ropyl, 2-methoxy-l-methyl-ethyl, 2-propyloxyethyl, 2-isopropyloxyethyl, 2-ethoxypropyl, 2-ethoxy-l-methylethyl, 2-methoxybutyl, l-ethyl-2-methoxyethyl, 3-ethoxypropyl, 3-methoxybutyl, 3-methoxy-2-methylpropyl, 3-methoxy-1-methylpropyl, 2-butoxyethyl, 3-methoxy-3-methylbutyl, and 2-butoxy-l-methylethyl. The C2-C10 alkylthioalkyl represented by R8 or R9 may include, for example, methylthiomethyl, ethylthiomethyl, propylthiomethyl, isopropyl-thiomethyl, 2-methylthiomethyl, 1-methylthioethyl, 2-ethylthioethyl, 1-ethylthioethyl, 3-methylthiopropyl, 2-methylthiopropyl, 1-methylthiopro-pyl, 2-methylthio-l-methylethyl, 2-propylthioethyl, 2-isopropylthioethyl, 2-ethylthiopropyl, 2-ethylthio-l-methylethyl, 2-methylthiobutyl, l-ethyl-2-methylthioethyl, 3-ethylthiopropyl, 3-methylthiobutyl, 2-methyl-3-methyl-thiopropyl, l-methyl-3-methylthiopropyl, 4-methylthiobutyl, l-methyl-2-methylthiopropyl, 2-isobutylthioethyl, 2-sec-butylthioethyl, 3-isobutylthio-propyl, and 3-sec-butylthiopropyl. The C2-C6 alkenyloxy represented by R10, R17, or R18 may include, for example, allyloxy, 2-butenyloxy, 3-butenyloxy, l-methyl-2-propenyloxy, 2-methyl-2-propenyloxy, 2-pentenyloxy, 3-pentenyloxy, 4-pentenyloxy, l-methyl-2-butenyloxy, 2-methyl-2-butenyloxy, 3-methyl-2-butenyloxy, l-inethyl-3-butenyloxy, 2-methyl-3-butenyloxy, 3-methyl-3-butenyloxy, l-ethyl-2-propenyloxy, 2-ethyl-2-propenyloxy, 2-hexenyloxy, 3-hexenyloxy, 4-hexenyloxy, 5-hexenyloxy, l-methyl-2-pentenyloxy, 2-methyl-2-pentenyloxy, 3-methyl-2-pentenyloxy, 4-methyl-2-pentenyloxy, l-methyl-3-pentenyloxy, 2-methyl-3-pentenyloxy, 3-methyl-3-pentenyloxy, 4-methyl-3-pentenyloxy, l-methyl-4-pentenyloxy, 2-methyl-4-pentenyloxy, 3-methyl-4-pentenyloxy, and 4-methyl-4-pentenyloxy. The C2-C6 haloalkenyloxy represented by R10, R17, or R18 may include, for example, 3-chloro-2-propenyloxy, 3-bromo-2-propenyloxy, 2-chloro-2-pro-penyloxy, 2-bromo-2-propenyloxy, 3,3-dichloro-2-propenyloxy, 3,3-dibromo-2-propenyloxy, 3,3-difluoro-2-propenyloxy, 2,3-dichloro-2-propenyloxy, 2,3-di-bromo-2-propenyloxy, 2-chloromethyl-2-propenyloxy, 4-chloro-2-butenyloxy, 3-chloro-4,4,4-trifluoro-2-butenyloxy, 3-bromo-4,4,4-trifluoro-2-butenyloxy, 3,4-dichloro-4,4-difluoro-2-butenyloxy, 3,4,4,4-tetrafluoro-2-butenyloxy, 4,4-dichloro-3-butenyloxy, 4,4-dibromo-3-butenyloxy, 5,5-dichloro-4-pentenyloxy, 5,5-dibromo-4-pentenyloxy, 6,6-dichloro-5-hexenyloxy, and 6,6-dibrmo-5-hexenyloxy. The C2-C6 alkynyloxy represented by R10, R17 or R18 may include, for example, 2-propynyloxy, 2-butynyloxy, 3-butynyloxy, l-methyl-2-propynyloxy, 2-pentynyloxy, 3-pentynyloxy, 4-pentynyloxy, l-methyl-2-butynyloxy, l-methyl-3-butynyloxy, 2-methyl-3-butynyloxy, l-ethyl-2-propynyloxy, 2-hexynyloxy, 3-hexynyloxy, 4-hexynyloxy, 5-hexynyloxy, l-ethyl-2-butynyl-oxy, l-ethyl-3-butynyloxy, and 2-ethyl-3-butynyloxy. The C2-C6 haloalkynyloxy represented by R10, R17, or R18 may include, for example, 3-chloro-2-propynyloxy, 3-bromo-2-propynyloxy, 4-chloro-2-butynyloxy, 4-chloro-3-butynyloxy, 4-bromo-2-butynyloxy, 4-bromo-3-buty-nyloxy, 5-chloro-4-pentynyloxy, 4-chloro-l-methyl-2-butynyloxy, 4-chloro-l- inethyl-3-butynyloxy, 4-chloro-2-inethyl-3-butynyloxy, 5-bromo-4-pentynyl-oxy, 4-broino-l-inethyl-2-butynyloxy, 4-bromo-l-methyl-3-butynyloxy, 4-bro-mo-2-methyl-3-butynyloxy, 6-chloro-5-hexynyloxy, and 6-bromo-5-hexynyl-oxy. The (C1-C3 alkoxy)carbonyl represented by R10 may include, for example, methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, isopropyl-oxycarbonyl, n-butyloxycarbonyl, isobutyloxycarbonyl, sec-butyloxycarbonyl, tert-butyloxycarbonyl, n-pentyloxycarbonyl, isopentyloxycarbonyl, neopen-tyloxycarbonyl, tert-pentyloxycarbonyl, and 1-ethylpropyloxycarbonyl. The C1-C3 alkylthio represented by R17- or R18 may include methylthio, ethylthio, propylthio, and isopropylthio. The C1-C3 haloalkylthio represented by R17 or R18 may include, for example, trifluoromethylthio, difluoromethylthio, bromodifluoromethylthio, 2,2,2-trifluoroethylthio, 2-chloro-l,l,2-trifluoroethylthio, 2-bromo-l,l,2-tri-fluoroethylthio, 1,1,2,2-tetrafluoroethylthio, 2-chloroethylthio, 2-fluoroethyl-thio, 2-bromoethylthio, 1,1,2,2,2-pentafluoroethylthio, 3-fluoropropylthio, 3-chloropropylthio, 3-bromopropylthio, 2,2,3,3,3-pentafluoropropylthio, and 3,3,3-trifluoropropylthio. The C1-C2 alkylsulfinyl represented by R17 or R18 may include methylsulfinyl or ethylsulfinyl. The C1-C2 alkylsulfonyl represented by R17 or R18 may include methylsulfonyl and ethylsulfonyl. The C1-C2 haloalkylsulfinyl represented by R17 or R18 may include, for example, trifluoromethylsulfinyl, 2,2,2-trifluoroethylsulfinyl, and perfluoro-ethylsulfinyl. The C1-C2 haloalkylsulfonyl represented by R17 or R18 may include, for example, trifluoromethylsulfonyl, 2,2,2-trifluoroethylsulfonyl, and perfluoro-ethylsulfonyl. The C1-C3 hydroxyalkyl represented by R17 or R18 may include hydroxymethyl, 2-hydroxyethyl, and 3-hydroxypropyl. The C2-C4 alkoxyalkyl represented by R17 or R18 may include, for example, methoxymethyl, ethoxymethyl, propyloxymethyl, isopropyloxy-methyl, 2-methoxyethyl, 1-methoxyethyl, 2-ethoxyethyl, 1-ethoxyethyl, 3-methoxypropyl, 2-methoxypropyl, 1-methoxypropyl, and 2-methoxy-l-methylethyl. The C2-C4 alkylthioalkyl represented by R17 or R18 may include, for example, methylthiomethyl, ethylthiomethyl, propylthiomethyl, isopropyl- ' thiomethyl, 2-methylthioethyl, 1-methylthioethyl, 2-ethylthioethyl, 1-ethyl- thioethyl, 3-methylthiopropyl, 2-methylthiopropyl, 1-methylthiopropyl, and 2-methylthio-l-methylethyl. The (C1-C2 alkyl)aminocarbonyl represented by R17 may include methylaminocarbonyl or ethylaminocarbonyl. The di(Ci-C2 alkyl)aminocarbonyl represented by R^^ may include dimethylaminocarbonyl, N-methyl-N-ethylaminocarbonyl, or diethylamino-carbonyl. The (C1-C6 alkoxy)carbonyl represented by R17 may include, for example, methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, isopropyl- oxycarbonyl, n-butyloxycarbonyl, isobutyloxycarbonyl, sec-butyloxycarbonyl, tert-butyloxycarbonyl, n-pentyloxycarbonyl, isopentyloxycarbonyl, neopen-tyloxycarbonyl, tert-pentyloxycarbonyl, 1-ethylpropyloxycarbonyl, n-hexyl-oxycarbonyl, isohexyloxycarbonyl, 2-ethylbutyloxycarbonyl, 1-methylpentyl-oxycarbonyl, 1-ethylbutyloxycarbonyl, 3-methylpentyloxycarbonyl, and 1,3-dimethylbutylcarbonyl. The C2-C6 cycloalkenyl represented by R17 may include 1-cyclopen-tenyl, 2-cyclopentenyl, 3-cyclopentenyl, 1-cyclohexenyl, 2-cyclohexenyl, or 3-cyclohexenyl The C2-C6 cycloalkyloxy represented by R17 may include cyclopropyl-oxy, cyclobutyloxy, cyclopentyloxy, or cyclohexyloxy. The C5-C6 cycloalkenyloxy represented by R1 may include 1-cyclo-pentenyloxy, 2-cyclopentenyloxy, 3-cyclopentenyloxy, 1-cyclohexenyloxy, 2-cyclohexenyloxy, or 3-cyclohexenyloxy. The 3,3-dihalogeno-substituted-2-propenyl represented by R4 may include, for example, 3,3-dichloro-2-propenyl, 3,3-dibromo-2-propenyl, 3-bro-mo-3-chloro-2-propenyl, 3-chloro-3-fluoro-2-propenyl, and 3-bromo-3-fluoro-2-propenyL The C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, which is represented by R6, R8, or R9, may include, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 2-methylcyclopentyl, 3-methylcyclopentyl, 2-methyl-cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 4-ethylcyclohexyl, 4-n-propylcyclohexyl, 4-isopropylcyclohexyl, and 4-tert-butylcyclohexyl The C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, which is represented by R6, R8, or R9, may include, for example, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclo-hexylmethyl, 1-cyclopropylethyl, (2-methylcyclopropyl)methyl, 2-(2-methyl-cyclopropyl)ethyl, 2-cyclopentylethyl, 3-cyclopentylpropyl, 2-cyclohexylethyl, and 3-cyclohexylpropyl. The C3-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, which is represented by R6, R8, or R9, may include, for example, 2-cyclopentenyl, 3-cyclopentenyl, 2-cyclohexenyl, 3-cyclohexenyl, 3,5,5-trimethyl-2-cyclo-hexenyl, and 3-methyl-2-cyclohexenyl. The C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, which is represented by R6, R8, or R9, may include, for example, (l-cyclopentenyl)methyl, (2-cyclopentenyl)methyl, (1-cyclohexenyl)-methyl, (2-cyclohexenyl)methyl, (3-cyclophexenyl)methyl, and 2-(3-cyclo- n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, and isobutyl. The C1-C3 haloalkyl in the phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy, which is represented by R7 R15, R16, R17, R18, or R42, may include, for example, trifluo-romethyl, difluoromethyl, bromodifluoromethyl, 1-fluoroethyl, 1-chloroethyl, 1-bromoethyl, perfluoroethyl, 2-bromo-l,l,2,2-tetrafluoroethyl, 1,1,2,2-tetra-fluoroethyl, 2-chloro-l,l,2-trifluoroethyl, 2-bromo-l,l,2-trifluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, 2-fluoroethyl, 2-chlo-roethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoropropyl, l,l,l,3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bromopropyl, 2-iodopropyl, and 2,3-dibromopropyl. romethoxy, bromodifluoromethoxy, 1-fluoroethoxy, 1-chloroethoxy, 1-bromo-ethoxy, perfluoroethoxy, 2-bromo-l,l>2,2-tetrafliioroethoxy, 1,1,2,2-tetrafluo-roethoxy, 2-chloro-l,l,2-trifluoroethoxy, 2-bromo-l,l,2-trifluoroethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy, 2,2,2-tribromoethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2-dichloro-ethoxy, 2,2-dibromoethoxy, 3-fluoropropyloxy, 3-chloropropyloxy, 3-bromo-propyloxy, 3-iodopropyloxy, 3,3,3-trifluoropropyloxy, 2,2,2,3,3,3-hexafluoro-propyloxy, l,l,l,3,3,3-hexafluoro-2-propyloxy, 2-fluoropropyloxy, 2-chloropro-pyloxy, 2-bromopropyloxy, 2-iodopropyloxy, and 2,3-dibromopropyloxy. The halogen in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R7, R16, R17, or R42, may include fluorine, chlorine, bromine, or iodine. The C1-C4 alkyl in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R7, R16, R17, or R42, may include methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, and isobutyl. The C1-C3 haloalkyl in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring ' thereof, which is represented by R7, R16, R17, or R42, may include, for example, trifluoromethyl, difluoromethyl, bromodifluoromethyl, 1-fluoroethyl, 1-chloroethyl, 1-bromoethyl, perfluoroethyl, 2-bromo-l,l,2,2-tetrafluoroethyl, 1,1,2,2-tetrafluoroethyl, 2-chloro-l,l,2-trifluoroethyl, 2-bromo-l,l,2-trifluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, - 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoro-propyl, l,l,l,3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bro- mopropyl, 2-iodopropyl, and 2,3-dibromopropyl. The C1-C3 alkoxy in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R7, R16, R17 or R42, may include methoxy, ethoxy, n-propyloxy, or isopropyloxy The C1-C3 haloalkoxy in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R7, R16, R17, or R42, may include, for example, trifluoromethoxy, bromodifluoromethoxy, 1-fluoroethoxy, 1-chlo-roethoxy, 1-bromoethoxy, perfluoroethoxy, 2-bromo-l,l,2,2-tetrafluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-chloro-l,l,2-trifluoroethoxy, 2-bromo-l,l,2-tri-luoroethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy, 2,2,2-tribromo-ethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-di-fluoroethoxy, 2,2-dichloroethoxy, 2,2-dibromoethoxy, 3-fluoropropyloxy, 3-chloropropyloxy, 3-bromopropyloxy, 3-iodopropyloxy, 3,3,3-trifluoropro-pyloxy, 2,2,2,3,3,3-hexafluoropropyloxy, 1,1,1,3,3,3-hexafluoro-2-propyloxy, 2-fluoropropyloxy, 2-chloropropyloxy, 2-bromopropyloxy, 2-iodopropyloxy, and 2,3-dibormopropyloxy. The halogen in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R17, may include fluorine, chlorine, bromine, or iodine. The C1-C4 alkyl in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R17, may include methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, and isobutyl. The C1-C3 haloalkyl in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 halo- alkoxy on the ring thereof, which is represented by R17, may include, for example, trifluoromethyl, difluoromethyl, bromodifluoromethyl, 1-fluoro-ethyl, 1-chloroethyl, 1-bromoethyl, perfluoroethyl, 2-bromo-l,l,2,2-tetra-fluoroethyl, 1,1,2,2-tetrafluoroethyl, 2-chloro-l,l,2-trifluoroethyl, 2-bromo- 1,1,2-trifluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromo-ethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoro-ethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoro-propyl, l,l,l,3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bro-mopropyl, 2-iodopropyl, and 2,3-dibromopropyL The C1-C3 alkoxy in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R17 may include methoxy, ethoxy, n-propyloxy, or isopropyloxy. The C1-C3 haloalkoxy in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R17, may include, for example, trifluoromethoxy, bromodifluoromethoxy, 1-fluoroethoxy, 1-chloroethoxy, 1-bromoethoxy, perfluoroethoxy, 2-bromo-l,l,2,2-tetrafluoro-ethoxy, 1,1,2,2-tetrafluoroethoxy, 2-chloro-l,l,2-trifluoroethoxy, 2-bromo-1,1,2-trifluoroethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy, 2,2,2-tri-bromoethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2-dichloroethoxy, 2,2-dibromoethoxy, 3-fluoropropyloxy, 3-chloropropyloxy, 3-bromopropyloxy, 3-iodopropyloxy, 3,3,3-trifluoropropyl-oxy, 2,2,2,3,3,3-hexafluoropropyloxy, l,l,l,3,3,3-hexafluoro-2-propyloxy, 2-fluoropropyloxy, 2-chloropropyloxy, 2-bromopropyloxy, 2-iodopropyloxy, and 2,3-dibormopropyloxy. The halogen in the methylenedioxy optionally substituted with halogen or C1-C3 alkyl, which is represented by R17 and which is formed from two adjacent R17's combined together at their ends when b is 2 to 5, may include fluorine, chlorine, bromine, or iodine. The C1-C3 alkyl in the methylenedioxy optionally substituted with halogen or C1-C3 alkyl, which is represented by R17 and which is formed from two adjacent R17's combined together at their ends when b is 2 to 5, may include methyl, ethyl, n-propyl, and isopropyl. The halogen in the ethylenedioxy optionally substituted with halogen or C1-C4 alkyl, which is represented by R17 and which is formed from two ' adjacent R17's combined together at their ends when b is 2 to 5, may include fluorine, chlorine, bromine, or iodine. The C1-C3 alkyl in the ethylenedioxy optionally substituted with halogen or C1-C3 alkyl, which is represented by R17 and which is formed from two adjacent R17's combined together at their ends when b is 2 to 5, may - include methyl, ethyl, n-propyl, and isopropyl. R8 and R9, when combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring thereof, represent tetramethylene optionally substituted with C1-C4 alkyl or halogen; pentamethylene optionally substituted ■ with C1-C4 alkyl or halogen; butenylene optionally substituted with C1-C4 alkyl or halogen; pentenylene optionally substituted with C1-C4 alkyl or halogen; or pentadienylene optionally substituted with C1-C4 alkyl or halogen; examples of which are tetramethylene, 1-methyltetramethylene, 2-methyltetramethylene, 1,1-dimethyltetramethylene, 1,3-dimethyltetra-methylene, pentamethylene, 1-methylpentamethylene, 2-methylpentameth-ylene, 3-methylpentamethylene, 3-ethylpentamethylene, 3-tert-butylpenta-methylene, 1,1-dimethylpentamethylene, 1,5-dimethylpentamethylene, 1-chloropentamethylene, 1-methoxypentamethylene, 1-butenylene, 1-methyl-l-butenylene, 2-methyl-l-butenylene, 1-pentenylene, 2-methyl-l-pentenylene, 3,3-dimethyl-l-pentenylene, 2-oxa-l-methyltetramethylene, 3-oxapentamethylene, 3-oxa-l,4-pentadienylene, 2-thiatetramethylene, 3-thiapentainethylene, 3,3-dimethyl-2,4-dioxapentainethylene, and 2,4-dithiapentamethylene. In these groups, each methylene or methine linkage may be replaced with an oxygen or sulfur atom. The C2-C6 cycloalkylene represented by E may include 1,2-cyclo-hexylene, 1,3-cyclohexylene, 1,4-cyclohexylene, 1,2-cyclopentylene, and 1,3-cyclopentylene. The C1-C3 alkyl substituted with cyano, nitro, (C1-C4 alkoxy)carbonyl, C1-C4 alkylthio, or C1-C4 alkoxy, which is represented by R6, may include, for example, cyanomethyl, 1-cyanoethyl, 2-cyanoethyl, 3-cyanopropyl, nitro-methyl, 1-nitroethyl, 1-methyl-l-nitroethyl, methoxycarbonylmethyl, ethoxy-carbonylmethyl, isopropoxycarbonylmethyl, l-(methoxycarbonyl)ethyl, 2-(methoxycarbonyl)ethyl, methoxymethyl, ethoxymethyl, 1-methoxyethyl, 2-methoxyethyl, 2-ethoxyethyl, 2,2-dimethoxyethyl, 2,2-diethoxyethyl, 2,2-dimethoxypropyl, 2,2-diethoxypropyl, 3,3-dimethoxypropyl, 3,3-diethoxy-propyl, 2,3-dimethoxypropyl, methylthiomethyl, 2-methylthioethyl, and 2,2-di(methylthio)ethyL In the case where h is 0 and i is 1 in A1-1, R22 and R7, when combined together at their ends to form trimethylene, tetramethylene, or penta-methylene, which is optionally substituted with C1-C3 alkyl, may include, for example, trimethylene, 1-methyltrimethylene, 2-methyltrimethylene, tetramethylene, 1-methyltetramethylene, 2-methyltetramethylene, and penta-methylene. In the case where h is 0 and j is 1 in A1-2, A1-3, A1-4, A1-5, or A1-6, R22 and R7, when combined together at their ends to form trimethylene, tetramethylene, or pentamethylene, which is optionally substituted with C1-C3 alkyl, may include, for example, trimethylene, 1-methyltrimethylene, 2-methyltrimethylene, tetramethylene, 1-methyltetramethylene, 2-methyl-tetramethylene, and pentamethylene. Preferred examples of the present compounds are as follows: oxime compounds of formula (1) wherein X is X1; oxime compounds of formula (1) wherein X is X1 and A1 is A1-1, A1-2, A1-3,A1-4,,A1-5, or A1-6; or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C5-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or C6-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof; oxime compounds of formula (1) wherein X is X1 R7 is hydrogen, C1-C6 alkyl, or C1-C3 haloalkyl, oxime compounds of formula (1) wherein X is X1 R7 is hydrogen, C1-C6 alkyl, or C1-C3 haloalkyl, A1 is A1-3, or A1 is A1-2 and k is an integer of 2 to 6, Q1 is oxygen, and R6 is C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, C2-C6 haloalkenyl, C3-C6 alkynyl, or Cg-Ce haloalkynyl, or Cg-C, cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C5-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or C3-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or T1-l or T1-2; oxime compounds of formula (1) wherein R2 and R3 are independently chlorine or C1-C3 alkyl, a is 0, R4 is 3,3-dichloro-2-propenyl or 3,3-dibromo-2-propenyl, R4 is 3,3-dichloro-2-propenyl, R6 is isopropyl, isobutyl, sec-butyl, tert-butyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, l,l,l,3,3,3-hexafluoro-2-propyl, or 3,3-dichloro-2-propenyl, and R7 is hydrogen; oxime compounds of formula (1) wherein X is X1 A1 is A1-2, R21 R22 R23 and R24 are all hydrogen, h is 0, Q1 is oxygen, j is 1, k is an integer of 3 to 6, Y and Z are both oxygen, W is a benzene ring, a heterocyclic 6-membered ring containing at least oxygen, sulfur, or nitrogen atom, a heterocyclic 5-membered ring containing at least one oxygen, sulfur, or nitrogen atom, or any one of these rings substituted with one to four identical or different (R40)g2's, wherein R40 is halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy, and g2 is an integer of 1 to 4; oxime compounds of formula (1) wherein A1 is A1-7, A1-8, A1-9, A1-10, A1.ll,or A1-12, and W is a benzene ring, a pyridine ring, a pyridazine ring, a pyrimidine ring, a pyradine ring, a furan ring, a thiophene ring, a pyrrole ring, an oxazole ring, an isoxazole ring, a thiazole ring, an isothiazole ring, a pyrazole ring, an imidazole ring, or any one of these rings substituted with one to four identical or different (R40)g2's; oxime compounds of formula (1) wherein A1 is A1-7, A1-8, A1-9, A1-10, A1-ll, or A1-12, and W is a benzene ring, a pyridine ring, a pyridazine ring, or any one of oxime compounds of formula (1) wherein X is X2; oxime compounds of formula (1) wherein X is X2, and Y and Z are both oxygen; oxime compounds of formula (1) wherein X is X2 and a is 0; oxime compounds of formula (1) wherein X is X2, and R1 R2, and R3 are independently halogen or C1-C3 alkyl; oxime compounds of formula (1) wherein A2 is A2-1; oxime compounds of formula (1) wherein A2 is A2-2 and Q1 is oxygen; oxime compounds of formula (1) wherein A2 is A2-3 and Q2 is oxygen; oxime compounds of formula (1) wherein A2 is A2--4, and Q2 and Q3 are or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C5-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or C6-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on or a heterocyclic 6-membered ring, exclusive of pyridine ring, containing at least one oxygen, sulfur, or nitrogen atom, which heterocyclic 6-membered ring may be optionally substituted with one to three identical or different (R18)g's, and R18 and g are as defined above, or a heterocyclic 5-membered ring containing at least one oxygen, sulfur, or nitrogen atom, which heterocyclic 5-membered ring may be optionally substituted with one to three identical or different (R18)g's, and R18 and g are as defined above, or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring thereof; oxime compounds of formula (1) wherein X is X2, and R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C2-C10 alkoxyalkyl, C2-C10 alkylthioalkyl, or naphthyl, or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C2-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on wherein R17, D, R11 R12, b, and d are as defined above, or 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, or 3-pyrrolyl, each of which heterocyclic groups may be optionally substituted with one to three identical or different (R18) wherein R18 and g are as defined above, or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring thereof; oxime compounds of formula (1) wherein X is X2, and R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C3-C6 haloalkynyl, C2-C10 alkoxyalkyl, or C2-C10 alkylthioalkyl, or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C2-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or T2-1 or T2-2 of formula (4) T2.I T2.2 wherein R17, D, R11 R12, b, and d are as defined above, or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring thereof; oxime compounds of formula (1) wherein X is X2, and R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C3-C6 haloalkynyl, C2-C10 alkoxyalkyl, or C2-C10 alkylthioalkyl, or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C2-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or C6-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring thereof; and oxime compounds of formula (1) wherein X is X2, and R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C2-C10 alkoxyalkyl, or C2-C10 alkylthioalkyl, or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C3-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof. Particularly preferred examples of the present compounds are as follows: (187) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta- nal 0-isopropyloxime (169) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta- nal 0-isopropyIoxime (188) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa- nal 0-isopropyloxime (26) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-nal 0-tert-butyloxime (16) 5-(2,6-dicliloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta- nal 0-tert-butyloxime (134) 6-(2,6-dicliloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-tert-butyloxime (189) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta- nal 0-(2,2,2-trichloroethyl)oxime (170) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta- nal 0-(2,2,2-trichloroethyl)oxime (190) 6-(2,6-dicliloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa- nal 0-(2,2,2-trichloroethyl)oxime (24) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-nal 0-(3,3-dichloro-2-propenyl)oxime (17) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta- nal 0-(3,3-dichloro-2-propenyl)oxime (76) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-(3,3-dichloro-2-propenyl)oxime (165) 4-(2,6-diehloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-isopropyloxime (152) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl- oxyacetaldehyde 0-isopropyloxime (191) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl- oxyacetone 0-isopropyloxime (172) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl oxyacetone 0-isopropyloxime (6) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl- oxyacetaldehyde 0-tert-butyloxime (14) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl- oxyacetaldehyde 0-tert-butyloxime (103) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-tert-butyloxime (104) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-tert-butyloxime (167) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime (160) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime (192) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl- oxyacetone 0-(2,2,2-trichloroethyl)oxime (173) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl- oxyacetone 0-(2,2,2-trichloroethyl)oxime (2) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl- oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (15) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl- oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (46) 4-(2,6-dichloro-4-(3,3-dichIoro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime (47) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl- oxyacetone 0-(3,3-dichloro-2-propenyl)oxime (329) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-ylbenzaldehyde 0-sec-butyloxime (314) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- ylbenzaldehyde 0-t-butyloxime (355) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-sec-butyloxime (357) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-allyloxime (358) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxiine (338) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-n-propyloxime (339) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-isopropyloxime (340) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde O-sec-butyloxime (291) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-t-butyloxime (293) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-ethyloxime (318) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propiophenone 0-ethyloxime (297) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-ethyloxime (310) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-n-propyloxime (315) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyloxy)benzaldehyde 0-isopropyloxime (391) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-2,2,2-trifluoroacetophenone 0-ethyloxime (529) 4-(trifluoromethyl)benzaldehyde 0-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime (531) 4'-(trifluoromethyl)acetophenone 0-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime (545) trimethylacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (559) 3,3-dimethyl-2-butanoneO-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (562) 3,3-dimethyl-2-butanone O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (563) 4-methyl-2-pentanone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (564) 4-methyl-2-pentanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (582) 3-methyl-2-butanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime The above numbers preceding the compound names are also used below for designating the present compounds. The present compounds can be produced, for example, by the following production processes A to M. Production process A (the compounds of formula (1) wherein X is X1 and R6 is hydrogen are excluded) This is the production process in which a compound of formula (15) wherein R4 is as defined above and L is halogen (e.g., chlorine, bromine, iodine), mesyloxy, or tosyloxy. The reaction is preferably effected in the presence of an appropriate base and in an inert solvent. The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture. The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (15). The reaction temperature, although it can be usually selected in the range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of -5°C to the boiling point of the solvent used in the reaction or 100°C. The molar ratio of the starting materials and base to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process B (for the present compounds wherein Y is oxygen, with the proviso that when X is X1 R6 is not hydrogen) This is the production process in which the compound of formula (15) wherein Y is oxygen is reacted with an alcohol compound of formula (17) HO-R4 wherein R4 is as defined above. The reaction is preferably effected in the presence of an appropriate dehydrating agent and, if necessary, in an inert solvent. The dehydrating agent which can be used may include, for example, dicyclohexylcarbodiimide, dialkyl (e.g., C1-C4) azodicarboxylate (e.g., diethyl- azodicarboxylate, and diisopropylazodicarboxylate) - trialkyl (e.g., C1-C20) phosphine or triarylphosphine (e.g., triphenylphosphine, trioctylphosphine, tributylphosphine) systems. The solvent which can be used may include, for example, hydro-' carbons such as benzene, xylene, and toluene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, and dioxane; and halogenated hydrocarbons such as carbon tetrachloride, dichloromethane, chlorobenzene, and dichlorobenzene. The reaction temperature can be usually selected in the range of -20°C to 200°C or the boiling point of a solvent used in the reaction. The molar ratio of the starting materials and base to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process C (for the present compounds wherein Y and Z are both oxygen, with the proviso that when X is X1 R6 is not hydrogen) This is the production process in which a compound of formula (18) wherein R1 R2, R3, R4 and a are as defined above, is reacted with a compound of formula (19) wherein X and L are as defined above, with the proviso that when X is X1 R6 is hydrogen. The reaction is preferably effected in the presence of an appropriate base and in an inert solvent. The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture. The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (18). The reaction temperature, although it can be usually selected in the range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of -5°C to the boiling point of the solvent used in the reaction or 100°C. The molar ratio of the starting materials and base to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process D (for the present compounds wherein Y and Z are both oxygen, with the proviso that when X is X1 R6 is not hydrogen) This is the production process in which a compound of formula (18) is reacted with a compound of formula (20) X-OH wherein X is as defined above, with the proviso that when X is X1 R6 is not hydrogen. The reaction is preferably effected in the presence of an appropriate dehydrating agent and, if necessary, in an inert solvent. The dehydrating agent which can be used may include, for example, dicyclohexylcarbodiimide, dialkyl (e.g., C1-C4) azodicarboxylate (e.g., diethyl-azodicarboxylate, and diisopropylazodicarboxylate) - trialkyl (e.g., C1-C20) phosphine or triarylphosphine (e.g., triphenylphosphine, trioctylphosphine, tributylphosphine) systems. The solvent which can be used may include, for example, hydrocarbons such as benzene, xylene, and toluene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, and dioxane; and halogenated hydrocarbons such as carbon tetrachloride, dichloromethane, chlorobenzene, and dichlorobenzene. The reaction temperature can be usually selected in the range of -20°C to 200°C or the boiling point of a solvent used in the reaction. The molar ratio of starting materials and dehydrating agent to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process E (for the present compounds wherein X is X1) This is the production process in which a hydroxylamine compound of formula (21) R6O-NH2 wherein R6 is as defined above, or a salt thereof, is reacted with a carbonyl compound of formula (22) wherein R1 R2 R3, R4 R7 A1 Y, Z, and a are as defined above. The reaction can be effected in an inert solvent and, if necessary, in the presence of a base or an acid. The solvent which can be used may include, for example, alcohols such as methanol and ethanol; ethers such as diethyl ether, tetrahydrofuran, and dioxane; acetic acid; and water. If necessary, these solvents may also be used in admixture. The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. The amount of base to be used, if necessary, in the reaction is preferably 1 mole or more relative to 1 mole of the hydroxylamine compound of formula (21). The organic bases such as triethylamine and pyridine can serve both as the base and as the solvent, when the reaction is effected with them in large excess relative to the hydroxylamine compound of formula (21). The acid which can be used may include, for example, hydrochloric acid, sulfuric acid, and p-toluenesulfonic acid. The acid can be used in the reaction at a catalytic amount ranging from 0.01 to 1 equivalent relative to the carbonyl compound of formula (22). The hydroxylamine compound as the starting material, although it can be used as such in the reaction, is usually used in the form of an inorganic acid salt, such as hydrochloride or sulfate. The reaction temperature, although it can be usually selected in the range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of 0°C to the boiling point of the solvent used in the reaction or 60°C. The molar ratio of the starting materials and reagents to be used in the reaction may be freely selected; however, it is favorable that the reaction of the carbonyl compound of formula (22) and the hydroxylamine compound of formula (21) or a salt thereof is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process F (for the present compounds wherein X is X1 with the proviso that R6 is not hydrogen, T1-4, T1-5, T1-6, or T1-7) This is the production process in which a compound of formula (23) present compound wherein X is X1 and R6 is hydrogen). The reaction is preferably effected in the presence of an appropriate base and in an inert solvent. The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture. The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0,01 to 1 mole relative to 1 mole of the compound of formula (24). The reaction temperature, although it can be usually selected in the range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of -5°C to the boiling point of the solvent used in the reaction or 100°C. The molar ratio of the starting materials and base to be used in the reaction may be freely selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process G (for the present compounds wherein Y and Z are both oxygen, X is X1 A^ is A1-8, and el is 0, with the proviso that R6 is not hydrogen) wherein R6, R7, G1 and W are as defined above, Q4 is oxygen, sulfur, or NR39, and R39 is as defined above. The reaction is preferably effected in the presence of an appropriate base and in an inert solvent. The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture. The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, sodium carbonate, potassium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (25). The reaction temperature can be usually selected in the range of -20°C to the boiling point of a solvent used in the reaction or 150°C. The molar ratio of the starting materials and base to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process H (for the present compounds wherein Y and Z - are both oxygen, X is X2, A2 is A2-4, and el is 0) This is the production process in which a compound of formula (27) The reaction is preferably effected in the presence of an appropriate base and in an inert solvent. The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as - toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture. The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, sodium carbonate, potassium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (27). The reaction temperature can be usually selected in the range of -20°C to the boiling point of a solvent used in the reaction or 150°C. The molar ratio of the starting materials and base to be used in the reaction may be freely selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process I (for the present compounds wherein X is X2) This is the production process in which an 0-substituted hydroxyl-amine compound of formula (29) the presence of a base. The solvent which can be used may include, for example, alcohols such as methanol and ethanol; ethers such as diethyl ether, tetrahydrofuran, and dioxane; pyridine; and water. The carbonyl compound of formula (30) may also be used as the solvent. If necessary, these solvents may also be used in admixture. The base which can be used may include, for example, triethylamine, pyridine, and sodium acetate. The 0-substituted hydroxylamine compound as the starting material is usually used in the form of an inorganic acid salt such as hydrochloride. The reaction temperature is usually in the range of 0°C to 150°C. The molar ratio of the starting materials and reagents to be used in the reaction may be suitably selected; however, it is preferred that the reaction of the carbonyl compound of formula (30) and the 0-substituted hydroxylamine compound of formula (29) or a salt thereof is effected at the equimolar ratio or a ratio close thereto. The amount of base to be used, if necessary, in the reaction is preferably 1 mole or more relative to 1 mole of the compound of formula (29). After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process J (for the present compounds wherein X is X2) This is the production process in which a compound of formula (31) The reaction is preferably effected in the presence of an appropriate base and in an inert solvent. The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture. The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, sodium carbonate, potassium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (31). The reaction temperature can be usually selected in the range of -20°C to the boiling point of a solvent used in the reaction or 150°C. The molar ratio of the starting materials and base to be used in the reaction may be freely selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process K (for the compounds wherein X is X1 and R6 is T1-4, T1-5, or T1-7) wherein R15 and L1 are as defined above (when R6 is T1-7), is reacted with a compound of formula (24). The reaction is preferably effected in the presence of an appropriate base and in an inert solvent. The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture. The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-04) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In particular, organic bases such as triethylamine or pyridine are preferably used. The reaction temperature, although it can be usually selected in the range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of -5°C to the boiling point of the solvent used in the reaction or 50°C. The molar ratio of the starting materials and base to be used in the reaction may be freely selected; however, it is favorable that the reaction is effected with the compound of formula (33), (34), (35), or (36) and the base in an amount of 1 to 5 moles, respectively, relative to 1 mole of the compound of formula (24). After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process L (for the present compounds wherein X is X1 and R6 is T1-G) This is the production process in which an isocyanate compound or an isothiocyanate compound of formula (37) wherein J and R16 are as defined above, is reacted with a compound of formula (24). The reaction is effected, if necessary, in the presence of an appropriate catalyst and in an inert solvent. The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; and hydrocarbons such as toluene, benzene, and xylene. If necessary, these solvents may also be used in admixture. As the catalyst, for example, bases such as triethylamine, pyridine, and sodium acetate, or acids such as aluminum chloride, hydrogen chloride, and boron trifluoride ether complex (BF3.(C2H5)20), can be used. The reaction temperature, although it can be usually selected in the range of -20°C to the boiling point of a solvent used in the reaction, is more preferably in the range of-5°C to the boiling point of the solvent used in the reaction. The molar ratio of the starting materials be used in the reaction may be freely selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto. After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. Production process M (for the present compounds wherein X is X1 and R6 is tert-butyl) This is the production process in which isobutene (CH2=C(CH3)2) is reacted with a compound of formula (24). The reaction is effected in the presence of an appropriate acid catalyst and in an inert solvent. The solvent which can be used may include, for example, hydrocarbons such as toluene, benzene, and xylene; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; ethers such as 1,2-dimethoxyethane, tetrahydrofuran, and dioxane, dialkyl (e.g., C1-C4) ethers (e.g., diethyl ether, diisopropyl ether); and esters such as ethyl acetate. If necessary, these solvents may also be used in admixture. The acid catalyst which can be used may include, for example, inorganic acids such as hydrochloric acid, hydrobromic acid, perchloric acid, sulfuric acid, nitric acid, and phosphoric acid; and organic acids such as trifluoroacetic acid, trichloroacetic acid, methanesulfonic acid, benzene-sulfonic acid, p-toluenesulfonic acid, and camphorsulfonic acid. In particular, sulfuric acid is preferably used. The reaction temperature although it can be usuallv selected in the range of -50°C to 50°C or the boiling point of a solvent used in the reaction, is usually in the range of 0°C to 30°C, The molar ratio of the starting materials to be used in the reaction may be suitably selected; however, the reaction is preferably effected with the use of isobutene in an amount of 1 mole or more relative to 1 mole of the compound of formula (24). After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization. For the present compounds, there may exist optical isomers based on the presence of at least one asymmetric carbon atom, and the optical isomers having biological activity, whether they are either in (+)-form or in (-)-form, and their mixtures at any ratio are, of course, included within the scope of the present invention. Furthermore, there may exist geometrical isomers based on the presence of at least one double bond, and the geometrical isomers having biological activity, whether they are either in cis-form or in trans-form, and their mixtures at any ratio are, of course, included within the scope of the present invention. The compounds of formula (12), which are useful as the intermediates for the production of the present compounds, also have insecticidal/-acaricidal activity and can therefore be formulated or used as the active ingredients of insecticidal/acaricidal agents, in the same manner as the case of the present compounds. The specific examples of the present compounds are shown below; however, the present compounds are not limited to these examples. In the above formulae, (R1)a, R2, R3 and M2 are as defined in Table 1 below, and R6 is as defined in Tables 2 to 19 below. The following will describe various processes for producing the intermediates in the production of the present compounds. The compounds of formula (15) as the intermediates for the production of the present compounds can be produced, for example, according to the following schemes I to VI. wherein all the variable are as defined above, with the proviso that R6 is not hydrogen. wherein all the variable are as defined above, with the proviso that R6 is not hydrogen. wherein TBDMSCl is tert-butyldimethylsillyl chloride, Z1 is oxygen or sulfur, and the other variables are as defined above, with the proviso that R6 is not hydrogen. wherein all the variables are as defined above, with the proviso that R6 is not hydrogen. The compounds of formula (18) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme VII. The halide compounds of formula (16) and alcohol compounds of formula (17), both as the intermediates for the production of the present compounds, are commercially available or can be produced, for example, according to the publications: J. Org. Chem., 56, 1037-1041 (1991); Izvest. Akad. Nauk S.S.S.R., Otdel. Khim. Nauk, IQfiQ, 447-451 [CA (Chemical Abstracts) vol. 54, 22344d]; and Doklady Akad. Nauk S.S.S.R. 132, 606-608 (1960) [CA (Chemical Abstracts) vol. 54, 22331h], or according to the following scheme VIII. The compounds of formula (19) or (20) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme IX or X. A1-3,A1-4,A1-5, or A1-6, The compounds of formula (22) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XI, XII, XIII, XIV, or XV. wherein Y1 is oxygen or NH, R52 is a protecting group for the hydroxyl group of phenol or for the amino group of aniline, such as benzoyl, acetyl, or tert-butylmethylsillyl (TBDMS), and the other variables are as defined above. wherein R53 is methyl or ethyl, R54 is a protecting group for the hydroxyl group of phenol, such as benzoyl or acetyl, and the other variables are as defined above. Scheme XIII (in the case where X is X1 A1 is A1-2, A1-3, A1-4, A1-5, or A1-6, Q1 Y, and Z are all oxygen, and R7 is methyl) wherein R53 is methyl or ethyl, R55 is a protecting group for the hydroxyl group of phenol, such as benzyl, DIBAL means diisobutylaluminum hydride, and the other variables are as defined above. wherein R55 is a protecting group for the hydroxyl group of phenol, such as benzyl, R56 is acetyl or benzoyl, PCC means pyridinium chlorocromate, and the other variables are as defined above. The compounds of formula (21) as the intermediateg for the production of the present compounds are commercially available or can be produced, for example, according to the following scheme XVI, wherein L^ is a leaving group such as halogen, hydroxysulfonyloxy, or 2,4,6-trimethylbenzenesulfonyloxy, and the other variables are as defined above. The compounds of formula (33), (34), (35), (36), or (37), as the intermediates for the production of the present compounds, are commercially available or can be produced by the methods widely known in the art or by the methods as described in the publications: [compounds of formula (33) wherein J is sulfur] J. Org. Chem,, 3Q, 1284 (1965); [compounds of formula (35) wherein J is oxygen] J. Am. Chem. Soc, 81, 714 (1959); [compounds of formula (35) wherein J is sulfurl Justus Liebies Ann. Chem., 590. 123 (1954). The compounds of formula (19) or (20) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XVII. The compounds of formula (39) can be produced, for example, according to the following schemes XVIII-1 to XVIII-9. A11-8:-G2-(CR19R=20)j-(CR23=CR24)h-(CR225R26)=(CR27=CR28)p wherein all the variables are as defined above. Scheme XVIII-3 (in the case where A^ is A^-11) The compounds of formula (25) as the intermediates for the production of the present compounds can be produced, for example, according to scheme XIV. The compounds of formula (26) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XX, The compounds of formula (21) as the intermediates for the produc-ion of the present compounds are commercially available or can be produced, for example, according to the following scheme XXL The carbonyl compounds of formula (22) as the intermediates for the production of the present compounds can be produced, for example, according to the following schemes XXI-1 to XXII-5. ■ Scheme XXII-2 (in the case where X is X1 A1 is A1-8, and Y and Z are both oxygen) Scheme XXII-3 (in the case where X is X1 R7 is hydrogen, W is W1 A1 is A1-8, G1 is G1-1, al is 0, and Y and Z are both oxygen) V wherein R105 is methyl or ethyl, W1 is a benzene ring or a heterocyclic ring containing no -NH- linkage in the ring thereof, and the other variables are as defined above. Scheme XXII-4 (in the case where X is X1 R1 is hydrogen, W is W1 A1 is A^-8, G1 is G1-1, al is 0, and Y and Z are both oxygen) wherein R108 is methyl or ethyl, or two R108 are combined together at their ends to form ethylene or trimethylene, and the other variables are as defined above. Scheme XXII-5 (in the case where X is X1 R7 is hydrogen, A1 is A1-7, G^ is G1-1, al is 0, W is W\ t, h, u, and p are 0, j is 1, R29 and R30 are both hydrogen, and Y and Z are both oxygen) The compounds of formula (24) as the intermediates for the produc-on of the present compounds can be produced, for example, according to the following scheme XXIII. Some of the compounds of formula (41), (42), or (43) are commercially available or can be produced according to the following schemes XXIV-1 to XXIV-4. wherein R106is methyl or ethyl, R107Ms C1-C6 alkyl, C3-C6 cycloalkyl, or phenyl or benzyl, each of which may be optionally substituted with C1-C4 alkyl or C1-C3 alkoxy, and the other variables are as defined above. Scheme XXIV-3 . wherein all the variables are as defined above. wherein all the variables are as defined above. The starting compounds of formula (47) wherein R109 and R110 are L1, Q4H, CHO, CH(0R108)2, CO2H, CO2R105 COCH3, or CH2L1 and the other variables are as defined above, which are used in the lemes XXII-3, XXII-4, XXII-5, XXIV-1, XXIV-2, XXIV-3, and XXIV-4, and ler compounds are commercially available or can be produced, for example, the methods as described in the following publications. In the case where W1 is a pyridazine ring: J. Heterocyclic Chem., 5, 845 (1968); Monatschefte fur Chem., 110, 365 (1979), etc. In the case where W1 is a pyrimidine ring: Justus Liebigs Ann. Chem., 684, 209 (1965); J. Heterocyclic Chem., 28, 1281 (1991); Chem. Ber., 97, 3407 (1964); J. Chem. Soc, 1965, 5467; Aust. J. Chem., 19, 2321 (1966), etc. In the case where W^ is a pyradine ring: J. Org. Chem., 54, 640 (1089) etc. In the case where W1 is an oxazole ring: J. Org Chem., 57, 4797 (1992) etc. In the case where W1 is an isoxazole ring: Chem. Pharm. Bull, 14, 92 (1966); Chem. Pharm. Bull, 14, 1277 (1966); Chem. Pharm. Bull., 19, 46 (1971); J. Chem. Res. Synop., 1994, 116; V Synthesis, 1976, 992, etc. In the case where W1 is a thiazole ring: J.Am. Chem. Soc, 72, 5221 (1950) etc. In the case where W1 is an isothiazole ring: J. Chem. Soc, 1959, 3061 etc. In the case where W1 is an imidazole ring: Tetrahedron Lett, 26, 1915 (1985) etc. In the case where W1 is a pyrazole ring: Chem. Ber., 112, 1712 (1979); Chem. Ber., 116, 1520 (1983); JP-A 63-185964/1988; Tetrahedron, 29, 441 (1973); J. Chem. Soc, Chem. Commun., 1969, 66; J Org. Chem., 35, 3451 (1970); Chem. Ber., 103, 2356 (1970), etc. The compounds of formula (19) or (20) wherein X is X2, as the intermediates for the production of the present compounds, can be produced, for example, according to the following scheme XXV. wherein L3 is halogen (e.g., chlorine, bromine, iodine), mesyloxy, or tosyloxy, R151 is a protecting group for alcohols, such as described in PROTECTIVE GROUPS IN ORGANIC SYNTHESIS, TW. Greene, RG.M. Wuts, A WILEY-INTERSCIENCE PUBLICATION, JOHN WILEY & SONS, INC., pp. 10-142; e.g., benzoyl, and the other variables are as defined above. The compounds of formula (48) or (49) in the scheme XXV can be produced, for example, according to the following schemes XXVT to XXXXIII. wherein L5 is halogen (e.g., chlorine, bromine, iodine), mesyloxy, or tosyloxy, Q8 is oxygen, sulfur, or NR33, R33 is hydrogen or C1-C3 alkyl, and the other variables are as defined above. Scheme XXVIII (in the case where A2 is A2-3 and U3 is U3-2) wherein all the variables are as defined above. wherein Q9 is oxygen, sulfur, or NR34, R34 is hydrogen or C1-C3 alkyl, and the other variables are as defined above. wherein R152 is a protecting group for alcohols (as described in PROTECTIVE GROUPS IN ORGANIC SYNTHESIS, TW. Greene, RG.M. Wuts, A WILEY-INTERSCIENCE PUBLICATION, JOHN WILEY & SONS, INC., pp. 10-142; as a protecting group selectively removable for R151 for example, when R151 is benzoyl, R152 is tetrahydropyranyl), and the other variables are as defined above. wherein R153 is a protecting group (as described in PROTECTIVE GROUPS IN ORGANIC SYNTHESIS, T.W. Greene, RG.M. Wuts, A WILEY-INTERSCIENCE PUBLICATION, JOHN WILEY & SONS, INC., pp. 143-170 and 277-405; for example, when Q4 is oxygen, R153 is benzoyl), and the other variables are as defined above. Scheme XXXIV (in the case where A2 is A2-5 and U3 is U3-2) wherein all the variables are as defined above. Scheme XXXV-1 (in the case where A2 is A2-5 and U3 is U3-3) wherein L5 is halogen (e.g., chlorine, bromine, iodine), mesyloxy, or tosyloxy, and the other variables are as defined above. Scheme XXXVIII (in the case where A2 is A2-7 and U3 is U3-2) wherein all the variables are as defined above. Scheme XXXIX-1 (in the case where A2 is A1-7 and U3 is U3-3) wherein all the variables are as defined above. Scheme XXXX (in the case where A2 is A2-8 and U3 is U3-2) wherein all the variables are as defined above. Scheme XXXXM (in the case where A' is A'-S and U' is U'-3) wherein all the variables are as defined above. The compounds of formula (27) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XXXXIV. wherein all the variables are as defined above. The compounds of formula (28) as the intermediates for the production of the present compounds can be produced, for example, according to the following schemes XXXXV to XXXXVIL The compounds of formula (29) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XXXXVIII. The compounds of formula (32) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XXXXIX. The harmful insects and harmful ticks and mites, against which the present compounds exhibit controlling activity, may include, for example, the following: The present compounds are satisfactorily effective for the control of various noxious insects, mites and ticks, examples of which are as follows: Hemiptera: Delphacidae such as Laodelphax striatellus, Nilaparvata lugenSy and Sogatella furcifera, Deltocephalidae such as Nephotettix cincticeps and Empoasca onukh, Aphididae such as Aphis gossypii and Myzus persicae, Pentatomidae, Aleyrodidae such as Trialeurodes vaporariorum, Bemisia tabaci, and Bemisia argentifolii, Coccidae, Tingidae, Psyllidae, etc. Lepidoptera: Pyralidae such as Chilo suppressalis, Cnaphalocrocis medinalis, Ostrinia nubilalis, and Parapediasia teterrella, Noctuidae such as Spodoptera litura, Spodoptera exigua, Pseudaletia separata, Mamestra brassicae, Agrotis ipsilon, Ttichoplusia spp., HeJiothisspp., Helicoverpa spp. and Earias spp., Pieridae such as Pieris rapae crucivora, Tortricidae such as Adoxophyes orana fasciata, Grapholita molesta, and Cydia pomonella, Carposinidae such as Carposina niponensis, Lyonetiidae such as Lyonetia clerkella, Gracillariidae such as Phyllonorycter ringoniella, Phyllocnistidae such as Phyllocnistis citrella, Yponomeutidae such as Plutella xylostella, Gelechiidae such as Pectinophora gossypiella, Arctiidae, Tineidae, etc. Biptera: CaJicidae, Aedes spp,, Anopheles spp., Chironomidae, Muscidae, Calliphoridae, Sarcophagidae, Anthomyiidae, Cecidomyiidae, Agromyzidae, Tephritidae, Brosophilidae, Psychodidae, Simuliidae, Tabanidae, Stomoxyidae, etc. Coleoptera: Chrysomelidaey Scarabaeidae, Curculionidae, Attelabidae, Coccinellidae, Cerambycidae, Tenebrionidae, etc. Thysanoptera: Thnpidae such as Thrips spp., e.g., Thrips palmi, Frankliniella spp., e.g., Frankliniella occidentalism Sciltothrips spp., e.g., Sciltothrips dorsalis, and Phlaeotberipidae, etc. Hymenoptera: Tenthredinidae, Formicidae, Vespidae, etc. Dictyoptera: Blattidae, Blattellidae, etc. Orthoptera: Acrididae, Gryllotalpidae, etc, Aphaniptera: Purex irritans etc. Anoplura: Pediculus humanus capitis etc. Isoptera: Termitidae etc, Acarina: Tetranychidae such as Tetranychus spp. and Panonychus spp,, Tarsonemidae, Eriophyidae, Acaridae, Ixodidae, etc. The present compounds are also effective for the control of various noxious insects, mites and ticks with resistance to conventional insecticides or acaricides. When the present compounds are used as the active ingredients of insecticidal/acaricidal agents, they may be used as such without addition of any other ingredients. The present compounds are, however, usually mixed with solid carriers, liquid carriers, gaseous carriers, or baits, and if necessary, with surfactants and other auxiliaries, and formulated into various forms, such as oil sprays, emulsifiable concentrates, wettable powders, flowables, granules, dusts, aerosols, fumigants (e.g., foggings), or poison baits. Each of these formulations may usually contain at least one of the present compounds as an active ingredient in an amount of 0.01% to 95% by weight. The solid carrier which can be used in the formulation may include, for example, fine powder or granules of clay materials such as kaolin clay, diatomaceous earth, synthetic hydrated silicon oxide, bentonite, Fubasami clay, and acid clay; various kinds of talc, ceramics, and other inorganic minerals such as sericite, quartz, sulfur, activated carbon, calcium carbonate, and hydrated silica; and chemical fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, urea, and ammonium chloride. The liquid carrier may include, for example, water; alcohols such as methanol and ethanol; ketones such as acetone and methyl ethyl ketone; hydrocarbons such as hexane, cyclohexane, kerosene, and light oil; esters such as ethyl acetate and butyl acetate; nitriles such as acetonitrile and isobutyronitrile; ethers such as diisopropyl ether and dioxane; acid amides such as N,N-dimethylformamide and N,N-dimethylacetamide; halogenated hydrocarbons such as dichloromethane, trichloroethane, and carbon tetrachloride; dimethyl sulfoxide; and vegetable oils such as soybean oil and cottonseed oil. The gaseous carrier or propellant may include, for example, Freon gas, butane gas, LPG (liquefied petroleum gas), dimethyl ether, and carbon dioxide. The surfactant may include, for example, alkyl sulfates, alkyl sulfonates, alkyl arylsulfonates, alkyl aryl ethers and their polyoxyethylene derivatives, polyethylene glycol ethers, polyhydric alcohol esters, and sugar alcohol derivatives. The auxiliaries such as fixing agents or dispersing agents may include, for example, casein, gelatin, polysaccharides such as starch, gum arabic, cellulose derivatives, and alginic acid, lignin derivatives, bentonite, sugars, and synthetic water-soluble polymers such as polyvinyl alcohol, polyvinyl pyrrolidone, and polyacrylic acid. The stabilizer may include, for example, PAP (isopropyl acid phosphate), BHT (2,6-di-tert-butyl-4-methylphenol), BHA (mixtures of 2-tert-butyl-4-methoxyphenol and 3-tert-butyl-4-methoxyphenol), vegetable oils, mineral oils, surfactants, fatty acids, and their esters. The base material for used in poison baits may include, for example, bait materials such as grain powder, vegetable oils, sugars, and crystalline cellulose; antioxidants such as dibutylhydroxytoluene and nordihydro-guaiaretic acid; preservatives such as dehydroacetic acid; substances for preventing erroneous eating, such as red pepper powder; attractant flavors such as cheese flavor or onion flavor. The formulations thus obtained are used as such or after diluted with water. Furthermore, they may be used in admixture with or separately but simultaneously with other insecticides, nematocides, acaricides, bactericides, fungicides, herbicides, plant growth regulators, synergists, fertilizers, soil conditioners and/or animal. The insecticide, nematocide and/or acaricide which can be used may include, for example, organophosphorus compounds such as Fenitrothion [0,0-dimethyl 0-(3-methyl-4-nitrophenyl)phosphorothioate], Fenthion [0,0-dimethyl 0-(3-methyl-4-(methylthio)phenyl)phophorothioate], Diazinon [0,0-diethyl-0-2-isopropyl-6-methylpyrimidin-4-ylphosphorothioate], Chlor-pyriphos [0,0-diethyl-0-3,5,6-trichloro-2-pyridylphosphorothioate], Ace-phate [0,S-dimethylacetylphosphoramidothioate], Methidathion [S-2,3-di- hydro-5-methoxy-2-oxo-l,3,4-thiadiazol-3-ylmethyl 0,0-dimethylphosphoro-dithioate], Disulfoton [0,0-diethyl S-2-ethylthioethylphosphorothioate], DDVP [2,2-dichlorovinyldimethylphosphate], Sulprofos [0-ethyl 0-4-(meth-ylthio)phenyl S-propyl phosphorodithioate], Cyanophos [0-4-cyanophenyl 0,0-dimethylphosphorothioate], Dioxabenzofos [2-methoxy-4H-l,3,2-benzo-dioxaphosphinine-2-sulfide], Dimethoate [0,0-dimethyl-S-(N-methylcar-bamoylmethyl)dithiophosphate], Phenthoate [ethyl 2-dimethoxyphosphino-thioylthio(phenyl)acetate], Malathion [diethyl(dimethoxyphosphinothioyl-thio)succinate], Trichlorfon [dimethyl 2,2,2-trichloro-l-hydroxyethylphos-phonate], Azinphos-methyl [S-3,4-dihydro-4-oxo-l,2,3-benzotriazin-3-yl-methyl 0,0-dimethylphosphorodithioate], Monocrotophos [dimethyl (E)-1-methyl-2-(methylcarbamoyl)vinylphosphate], Ethion [0,0,0',0'-tetraethyl S,S'-methylenebis(phosphorodithioate)], and Profenofos [0-4-bromo-2-chloro-phenyl 0-ethyl S-propyl phosphorothioate]; carbamate compounds such as BPMC (2-sec-butylphenylmethylcarbamate), Benfuracarb [ethyl N-[2,3-di-hydro-2,2-dimethylbenzofuran-7-yloxycarbonyl(methyl)aminothio]-N-isopro-pyl-p-alaninate], Propoxur [2-isopropoxyphenyl N-methylcarbamate], Car-bosulfan [2,3-dihydro-2,2-dimethyl-7-benzo[b]furanyl N-dibutylaminothio-N-methylcarbamate], Carbaril [1-naphthyl-N-methylcarbamate], Methomyl [S-methyl-N-[(methylcarbamoyl)oxy]thioacetimidate], Ethiofencarb [2-(eth-ylthiomethyl)phenylmethylcarbamate], Aldicarb [2-methyl-2-(methylthio)-propionaldehyde 0-methylcarbamoyloxime], Oxamyl [N,N-dimethyl-2-meth-ylcarbamoyloxyimino-2-(methylthio)acetamide], Fenothiocarb [S-4-phenoxy-butyl]-N,N-dimethylthiocarbamate], Thiodicarb [3,7,9,13-tetramethyl-5,11-dioxa-2,8,14-trithia-4,7,9,12-tetraazapentadeca-3,12-diene-6,10-dione], and Alanycarb [ethyl (Z)-N-benzyl-N-{[methyl(l-methylthioethylideneaminooxy-carbonyl)amino]thio}-p-alaninate]; pyrethroid compounds such as Etofen-prox [2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzylether], Fenvaler- ate [(RS)αcyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutyr-ate], Esfenvalerate [(S)-α-cyano-3-phenoxybenzyl (S)-2-(4-chlorophenyl)-3-methylbutyrate], Fenpropathrin [(RS)αcyano-3'phenoxybenzyl 2,2,3,3-tetramethylcyclopropanecarboxylate], Cypermethrin [(RS)αcyano-3-phe-noxybenzyl (lRS,3RS)-3-(2,2-dichlorovinyl)-2,2-diinethylcyclopropanecarbox-ylate], Permethrin [3-phenoxybenzyl (IRS, 3RS)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate], Cyhalothrin [(RS)αcyano-3-phenoxy-benzyl (Z)-(lRS)-cis-3-(2-chloro-3,3,3-trifluoroprop-l-enyl)-2,2-dimethylcyclo-propanecarboxylate], Deltamethrin [(S)αcyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate], Cycloprothrin [(RS)αcyano-3-phenoxybenzyl (RS)-2,2-dichloro-l-(4-ethoxyphenyl)cyclo-propanecarboxylate], Fluvalinate (a-cyano-3-phenoxybenzyl N-(2-chloro-a,a,a-trifluoro-p-tolyl)-D-valinate), Bifenthrin (2-methylbiphenyl-3-yl-methyl) (Z)-(lRS)-cis-3-(2-chloro-3,3,3-trifluoroprop-l-enyl)-2,2-dimethyl-cyclopropanecarboxylate), Acrinathrin [(S)αcyano-(3-phenoxyphenyl)-methyl [lR-{la(S),3α(Z)}]-2,2-dimethyl-3-[3-oxo-3-(2,2,2-trifluoro-l-(tri-fluoromethyl)ethoxy-l-propenyl)cyclopropanecarboxylate], 2-methyl-2-(4-bromodifluoromethoxyphenyl)propyl (3-phenoxybenzyl) ether, Traromethrin [(S)αcyano-3-phenoxylbenzyl(lR,3R)-3-[(rRS)(l,1,2',2'-tetrabromoethyl)]-2,2-dimethylcyclopropanecarboxylate], and Silafluofen [4-ethoxylphenyl [3-(4-fluoro-3-phenoxyphenyl)propyl]dimethylsilane]; thiadiazine derivatives such as Buprofezin (2-tert-butylimino-3-isopropyl-5-phenyl-l,3,5-thiadiazin-4-one; nitroimidazolidine derivatives such as Imidacloprid [l-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylidenamine]," Nereistoxin derivatives such as Cartap [S,S'-(2-dimethylaminotrimethylene)bis(thiocarbamate)], Thiocyclam [N,N-dimethyl-l,2,3-trithian-5-ylamine], and Bensultap [S,S'-2-dimethylaminotrimethylene di(benzenethiosulfonate)]; N-cyanoamidine derivatives such as acetamiprid [N-cyano-N'-methyl-N'-(6-chloro-3-pyridyl- methyl)acetamidine]; chlorinated hydrocarbon compounds such as Endo-sulfan [6,7,8,9,10,10-hexachloro-l,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepinoxide], yBHC (1,2,3,4,5,6-hexachlorocyclohexane), and l,l-bis(chlorophenyl)-2,2,2-trichloroethanol; benzoylphenylurea compounds such as Chlorfluazuron [l-(3,5-dichloro-4-(3-chloro-5-trifluoromethylpyridin-2-yloxy)phenyl)-3-(2,6-difluorobenzoyl)urea], Teflubenzuron [l-(3,5-dichloro-2,4-difluorophenyl)-3-(2,6-difluorobenzoyl)urea], and Fulphenoxron [l-(4-(2-chloro-4-trifluoromethylphenoxy)-2-fluorophenyl)-3-(2,6-difluorobenzoyl)-urea]; formamidine derivatives such as Amitraz [N,N'-[(methylimino)-dimethylidine]-di-2,4-xylidine], and Chlordimeform [N'-(4-chloro-2-methyl-phenyl)-N,N-dimethylmethanimidamide]; thiourea derivatives such as Diafenthiuron [N-(2,6-diisopropyl-4-phenoxyphenyl)-N'-tert-butylcarbodi-imide]; Bromopropylate [isopropyl 4,4'-dibromobenzylate], Tetradifon [4-chlorophenyl 2,4,5-trichlorophenylsulfone], Quinomethionate [S,S-6-methylquinoxaline-2,3-diyldithiocarbonate], Propargate [2-(4-tert-butyl-phenoxy)cyclohexyl prop-2-yl sulfite], Fenbutatin oxide [bis[tris(2-methyl-2-phenylpropyl)tin]oxide], Hexythiazox [(4RS,5RS)-5-(4-chlorophenyl)-N-chlorohexyl-4-methyl-2-oxo-l,3-thiazolidine-3-carboxamide], Chlofentezine [3,6-bis(2-chlorophenyl)-l,2,4,5-tetrazine], Pyridaben [2-tert-butyl-5-(4-tert-butylbenzylthio)-4-chloropyridazin-3(2H)-one], Fenpyroximate [tert-butyl (E)-4-[(l,3-dimethyl-5-phenoxypyrazol-4-yl)methyleneaminooxymethyl]-benzoate], Tebfenpyrad [N-4-tert-butylbenzyl]-4-chloro-3-ethyl-l-methyl-5-pyrazolecarboxamide], polynactin complexes [e.g., tetranactin, dinactin, trinactin]; Milbemectin, Avermectin, Ivermectin, Azadilactin [AZAD], Pyrimidifen [5-chloro-N-[2-{4-(2-ethoxyethyl)-2,3-dimethylphenoxy}ethyl]-6-ethylpyrimidin-4-amine], Chlorfenapyr [4-bromo-2-(4-chlorophenyl)-l-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile], Tebfenozide [N-tert-butyl-N'-{4-ethylbenzoyl)-3,5-dimethylbenzohydrazide], and phenylpyrazole derivatives. When the present compounds are used as the active ingredients of insecticidal/acaricidal agents for agriculture, the application amount thereof is usually in the range of 0.1 to 100 g per 10 ares. When they are used after diluted with water in the case of emulsifiable concentrates, wettable powders, flowables, or similar formulations, the application concentration thereof is usually in the range of 1 to 10,000 ppm. In the case of granules, dusts, or similar formulations, they are applied as such formulations without any dilution. When the present compounds are used as the active ingredients of insecticidal/acaricidal agents for epidemic prevention, they are usually applied after diluted with water to a typical concentration of 0.1 to 500 ppm in the case of emulsifiable concentrates, wettable powders, flowable, or similar formulations; or they are applied as such in the case of oil sprays, aerosols, fumigants, poisonous baits, or similar formulations. The application amount and concentration may vary depending upon the conditions including types of formulations, times, places and methods of application, kinds of noxious insects, mites and ticks, and degree of damage, and they can be increased or decreased without limitation to the above range. Examples The present invention will be further illustrated by the following production examples, formulation examples, and test examples; however, the present invention is not limited to these examples. The following are production examples for the present compounds. Production Example 1 Production of the present compound (2) by production process (E) To a mixture of 0.37 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyloxyacetaldehyde and 10 ml of pyridine was added 0.20 g of 0-(3,3-dichloro-2-propenyl)hydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.39 g (yield, 74%) of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.0 1.5489. Production Example 2 Production of the present compound (12) by production process F First, 0.27 g of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde oxime, O.lOg of potassium carbonate, 0.16 g of benzyl bromide, and 10 ml of N,N-dimethylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.21 g (yield, 56%) of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde 0-benzyloxime, nD22.5 1.5402. Production Example 3 Production of the present compound (16) by production process E To a mixture of 0.37 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentanal and 10 ml of pyridine was added 0.13 g of 0-tert-butylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.22 g (yield, 50%) of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal 0-tert-butyloxime, nD25.2 1.5275. Production Example 4 Production of the present compound (30) by production process E To a mixture of 0.34 g of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenoxy)acetone and 10 ml of pyridine was added 0.11 g of O-ethylhydroxyl-amine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.32 g (yield, 81%) of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 0-ethyloxime, m.p., 65.4°C. Production Example 5 Production of the present compound (14) by production process E To a mixture of 0.42 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyloxyacetaldehyde and 10 ml of pyridine was added 0.13 g of 0-tert-butylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.45 g (yield, 92%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetalde-hyde 0-tert-butyloxime, nD25.2 1.5185. Production Example 6 Production of the present compound (17) by production process E To a mixture of 0.37 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentanal and 10 ml of pyridine was added 0.20 g of 0-(3,3-di-chloro-2-propenyl)hydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.23 g (yield, 48%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal 0-(3,3-di-chloro-2-propenyl)oxime, nD25.2 1.5559. Production Example 7 Production of the present compound (74) by production process C First, 0.58 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol (which had been produced according to the method as disclosed in JP-A 8-337549/1996), 0.30 g of potassium carbonate, 0.43 g of chloroacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, and 10 ml of N,N-dimethylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography which afforded 0.74 g (yield, 82%) of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD22.3 1.5680. Production Example 8 Production of the present compound (147) by production process E To a mixture of 0.75 g of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyl- oxy)phenoxy)butyloxyacetaldehyde and 10 ml of pyridine was added 0.15 g of hydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0,67 g (yield, 75%) of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde oxime, nD24.5 1.5278. Production Example 9 Production of the present compound (152) by production process E To a mixture of 5.58 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentanal and 50 ml of pyridine was added 1.25 g of hydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 2.44 g (yield, 41%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal oxime, nD23.4 1.5600, Production Example 10 Production of the present compound (234) by production process E To a mixture of 1,67 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyloxyacetone and 30 ml of pyridine was added 8.60 g of hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concen- trated, which afforded 8.81 g (yield, 99%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone oxime, nD25.0 1.5460. Production Example 11 Production of the present compound (104) by production process E To a mixture of 0.43 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyloxyacetone and 10 ml of pyridine was added 0.15 g of 0-tert-butylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 0.45 g (yield, 90%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-tert-butyloxime, nD25.5 1.5170. Production Example 12 Production of the present compound (177) by production process K 6 First, 0,45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.12 g of triethylamine, and 10 ml of tetra-hydrofuran were placed in a reaction vessel, to which 0.12 g of acetic anhydride was slowly added dropwise with stirring at room temperature. After completion of the addition, the reaction mixture was further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with saturated aqueous sodium hydrogencarbonate solution and water in this order, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.21 g (yield, 43%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-acetyloxime, nD25.6 1.5318. Production Example 13 Production of the present compound (179) by production process K First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.12 g of triethylamine, and 10 ml of tetra-hydrofuran were placed in a reaction vessel, to which 0.25 g of 4-trifluoro-methylbenzoyl chloride was slowly added dropwise with stirring at room temperature. After completion of the addition, the reaction mixture was further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.59 g (yield, 96%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-(4-trifluoromethylbenzoyl)oxime, nD25.6 1.5300. Production Example 14 Production of the present compound (180) by production process K First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime and 10 ml of tetrahydrofuran were placed in a reaction vessel, to which 0.12 g of tert-butylisocyannate was slowly added dropwise with stirring at room temperature. After completion of the addition, the reaction mixture was further stirred at room temperature for 30 minutes, poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.47 g (yield, 86%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetone 0-(N-tert-butylcarbamoyl)oxime, nD25.6 1.5191. Production Example 15 Production of the present compound (216) by production process K First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.12 g of triethylamine, and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which a solution of 0.23 g of p-toluenesulfonyl chloride dissolved in 5 ml of tetrahydrofuran is slowly added dropwise with stirring under ice cooling. After completion of the addition, the reaction mixture is further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(p-toluenesulfonyl)oxime. Production Example 16 Production of the present compound (217) by production process K First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.12 g of triethylamine, and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which 0.16 g of N,N-diethyl-carbamoyl chloride is slowly added dropwise with stirring under ice cooling. After completion of the addition, the reaction mixture is further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel - chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyloxyacetone 0-(N,N-diethylcarbamoyl)oxime, Production Example 17 Production of the present compound (218) by production process L First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which 0.14 g of tert-butylisocyannate is slowly added dropwise with stirring at room temperature. After completion of the addition, the reaction mixture is further stirred at a temperature ranging from room temperature to 65°C, poured into water, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N-tert-butylthiocarbamoyl)oxime. Production Example 18 Production of the present compound (213) by production process F First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime and 10 ml of tert-butyl methyl ether are placed in a reaction vessel, to which 48 mg of 60% sodium hydride (in oil) is slowly added with stirring at room temperature in a stream of nitrogen gas. The mixture is stirred at room temperature until the evolution of hydrogen gas ceases, to which 0,11 g of chloroacetonitrile is added at room temperature, and the mixture is further stirred with heating under reflux. After completion of the reaction, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-cyanomethyloxime. Production Example 19 Production of the present compound (214) by production process F First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime and 10 ml of tert-butyl methyl ether are placed in a reaction vessel, to which 48 mg of 60% sodium hydride (in oil) is slowly added with stirring at room temperature in a stream of nitrogen gas. The mixture is stirred at room temperature until the evolution of hydrogen gas ceases, to which 0.29 g of tert-butyl bromoacetate is added at room temperature, and the mixture is further stirred with heating under reflux. After completion of the reaction, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-(tert-butoxycarbonyl-methyl)oxime. Production Example 20 Production of the present compound (211) by production process A First, 0.39 g of 5-(2,6-dichloro-4-hydroxyphnoxy)pentyloxyacetone 0-tert-butyloxime, 0.12 g of 1,1,3-tribromo-l-propene, 0.17 g of potassium carbonate, and 10 ml of N,N-dimethylformamide are placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dibromo-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-tert-butyloxime. Production Example 21 Production of the present compound (207) by production process C First, 0.46 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 0,25 g of potassium carbonate, 0.58 g of l-(5-(methanesulfonyloxy)pentyl-oxy)-2-butanone 0-tert-butyloxime, and 15 ml of N,N-dimethylformamide are placed in a reaction vessel. After stirring at 55°C to 60°C for 24 hours, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with ethyl acetate. The ethyl acetate layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 0.69 g (yield, 84%) of l-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)-2-butanone 0-tert-butyloxime, ND23.4 1.5140. Production Example 22 Production of the present compound (210) by production process D To a mixture of 0.45 g of 2-(5-hydroxypentyloxy)cyclohexane 0-tert-butyloxime, 0.43 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 0.39 g of triphenylphosphine, and 15 ml of tetrahydrofuran is slowly added dropwise 0.30 g of diisopropyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen gas. After stirring at room temperature for 24 hours, the reaction mixture is concentrated to give a residue. This residue is subjected to silica gel chromatography, which affords 2-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)cyclohexanone 0-tert-butyloxime. Production Example 23 Production of the present compound (103) by production process C First, 0.55 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 0.30 g of potassium carbonate, 0.59 g of 4-(methanesulfonyloxy)butyloxy-acetone 0-tert-butyloxime, and 10 ml of N,N-dimethylformamide are placed in a reaction vessel. After stirring at 60°0 for 6 hours, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with ethyl acetate. The ethyl acetate layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 0.71 g (yield, 77%) of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetone 0-tert-butyloxime, nD25.0 1.5170. Production Example 24 Production of the present compound (203) by production process D To a mixture of 0.51 g of 2-(2-hydroxyethoxy)ethoxyacetone 0-tert-butyloxime, 0,58 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 0.58 g of triphenylphosphine, and 20 ml of tetrahydrofuran is slowly added dropwise 0.49 g of diisopropyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen gas. After stirring at room temperature for 4 hours, the reaction mixture is concentrated to give a residue. This residue is subjected to silica gel chromatography, which affords 0.68 g (yield, 68%) of 2-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy)ethoxy-acetone 0-tert-butyloxime, nD23.0 1.5172. Production Example 25 Production of the present compound (104) by production process M First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.3 ml of concentrated sulfuric acid, and 10 ml of toluene are placed in a reaction vessel, into which isobutene gas is blown with stirring under ice cooling, and the mixture is further stirred at room temperature. After completion of the reaction, the reaction mixture is slowly poured into a saturated aqueous sodium hydrogencarbonate solution, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-tert-butyloxime. Production Example 26 Production of the present compound (185) by production process E To a mixture of 1.29 g of 0-(2,4,6-trimethylbenzenesulfonyl)hydroxyl-amine (which had been produced according to the method as described in Synthesis, 1-17 (1977)) and 10 ml of diethyl ether was added 1.14 g of sodium l,l,l,3,3,3-hexafluoro-2-propyloxide with stirring under ice cooling, and the mixture was stirred for 2 hours. The suspended reaction mixture was filtered through Celite to give a filtrate which was a solution of 0-(l,l,l, 3,3,3-hexafluoro-2-propyl)hydroxylamine in diethyl ether. The addition of diethyl ether to this filtrate made the diethyl ether solution have the weight of 30 g. Then, 10 g of the diethyl ether solution and 0.1 ml of concentrated hydrochloric acid were poured into a reaction vessel containing 0,37 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal. After stirring at room temperature for 2 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to preparative thin layer chromatography, which afforded 0.27 g (yield, 50%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentanal 0-(l,l,l,3,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4850. Production Example 27 Production of the present compound (186) by production process E A mixture of 0.34 g of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenoxy)acetone, 0.24 g of 0-(3-(5-trifluoromethyl-2-pyridyloxy)propyl)-hydroxylamine, 0.14 g of pyridinium chloride, and 10 ml of pyridine was stirred at room temperature for 2 hours. The reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 0.40 g (yield, 71%) of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-acetone 0-(3-(5-trifluoromethyl-2-pyridyloxy)propyl)oxime, nD23.0 1.5310. Production Example 28 Production of compound (279) by production process D To a mixture of 0.35 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenol, 0.32 g of 4-(hydroxy me thy l)benzaldehyde 0-(3,3-dichloro-2-prope-nyl)oxime, 0.32 g of triphenylphosphine, and 10 ml of dichloromethane was slowly added dropwise 0.25 g of diisopropyl azodicarboxylate. After stirring at room temperature for 12 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 0.43 g (yield, 67%) of 4-((2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)methyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 76.2°C. Production Example 29 Production of compound (293) by production process E To a mixture of 0.31 g of 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyloxy)acetophenone (which had been produced in Intermediate Production Example 2 as described below) and 10 ml of pyridine was added 0.07 g of 0-ethylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.33 g (yield, 99%) of 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)aceto-phenone 0-ethyloxime, nD24.5 1.5948. Production Example 30 Production of compound (303) by production process E To a mixture of 0.21 g of 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyloxy)benzaldehyde and 10 ml of pyridine was added 0.09 g of 0-ethylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.21 g (yield, 92%) of 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzaldehyde 0-ethyloxime, m.p., 42.6°C. Production Example 31 Production of compound (353) by production process E To a mixture of 0,55 g of 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)ethyl)benzaldehyde (which had been produced in Intermediate Production Example 3 as described below) and 5 ml of pyridine was added 0.18 g of 0-propylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.45 g (yield, 72%) of 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde 0-propyloxime, m.p., nD24.5 1.5773. Production Example 32 Production of compound (364) by production process E To a mixture of 0.41 g of 5-acetyl-2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)pyridine and 10 ml of pyridine was added 0.17 g of 0-ethylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.40 g (yield, 89%) of 5-(l-(N-ethoxyimino)ethyl)-2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenoxy)propyloxy)pyridine, nD24.5 1.5701. Production Example 33 Production of compound (369) by production process E To a mixture of 0.43 g of 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyl)benzaldehyde and 5 ml of pyridine was added 0.15 g of 0-tert-butylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.38 g (yield, 75%) of 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)benzaldehyde 0-tert-butyloxime, nD25.5 1.5673. Production Example 34 Production of compound (481) by production process D To a mixture of 0.62 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenol, 0.54 g of 5-(hydroxymethyl)-2-furfural 0-(3,3-dichloro-2-propenyl)- oxime, 0.57 g of triphenylphosphine, and 10 ml of dichloromethane was slowly added dropwise 0.44 g of diisopropyl azodicarboxylate with stirring under ice cooling. After stirring at room temperature for 12 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 0.43 g (yield, 69%) of 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyl)-2-furfural 0-(3,3-dichloro-2-propenyl)oxime, m.p., 65.0°C. Production Example 35 Production of compound (523) by production process I To a mixture of 0.15 g of benzaldehyde and 10 ml of pyridine was added 0.56 g of 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.50 g (yield, 79.4%) of benzaldehyde 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)-oxime, nD22..5 1.5797. Production Example 36 Production of compound (529) by production process I To a mixture of 0.14 g of 4-(trifluoromethyl)benzaldehyde and 10 ml of pyridine was added 0.30 g of 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0,37 g (yield, 95.6%) of 4-(trifluoromethyl)benzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD21..0 1.5387. Production Example 37 Production of compound (531) by production process I To a mixture of 0.15 g of 4'-(trifluoromethyl)acetophenone and 10 ml of pyridine was added 0.30 g of 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.30 g (yield, 75.5%) of 4'-(trifluoromethyl)acetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD21..5 1,5420. Production Example 38 Production of compound (545) by production process I To a mixture of 0.07 g of trimethylacetaldehyde and 5 ml of pyridine was added 0,30 g of 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.31 g (yield, 96.8%) of trimethylacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyl)oxime, nD23..0 1.5178. Production Example 39 Production of compound (564) by produc- tion process I To a mixture of 0.10 g of 4-methyl-2-pentanone and 5 ml of pyridine was added 0.40 g of 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0,42 g (yield, 95.4%) of 4-meth-yl-2-pentanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyl)oxime, nD24.5 1,5230. Some specific examples of the present compounds are shown below with their compound numbers and physical properties, if any. (1) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-ethyloxime, nD24.0 1.5310 (2) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(3,3-dichlorO-2-propenyl)oxime, nD24.0 1.5489 (3) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5661 (4) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(2-propenyl)oxime, nD23..5 1.5326 (5) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-benzyloxime, nD23..5 1.5471 (6) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-tert-butyloxime, nD23..5 1.5229 (7) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-methyloxime, nD23..5 1.5374 (8) (Z)-4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)- butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxiine, nD24.6 1.5498 (9) (E)-4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.6 1.5490 (10) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5213 (11) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-tert-butyloxime, nD24.5 1.4974 (12) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-benzyloxime, nD22.5 1.5402 (13) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(4-(trifluoromethyl)benzyl)oxime, nD22.5 1.5166 (14) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-tert-butyloxime, nD25.2 1.5185 (15) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD25.2 1.5450 (16) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-tert-butyloxime, nD25.2 1.5275 (17) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-(3,3-dichloro-2-propenyl)oxime, nD25.2 1,5559 (18) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-n-propyloxime, nD19.5 1.5373 (19) 5-(2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-(2-propenyl)oxime, nD19.5 1.5468 (20) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen tanal 0-(3,3-dibromo-2-propenyl)oxime, nD19.5 1.5742 (21) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-benzyloxime, nD23.7 1.5605 (22) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen tanal 0-(4-methoxybenzyl)oxime, nD21.5 1.5587 (23) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-(2,4-dinitrophenyl)oxime, m.p., 65.2°C (24) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-(3,3-dichloro-2-propenyl)oxime, nD22.6 1.5602 (25) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-(3,3-dibromo-2-propenyl)oxime, nD22.6 1.5797 (26) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-tert-butyloxime, nD22.6 1.5309 (27) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-benzyloxime, nD22.6 1.5700 (28) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-ethyloxime, nD24.6 1.5427 (29) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-methyloxime, nD22.6 1.5496 (30) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 0-ethyloxime, m.p., 65.4°C (31) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 0-(3,3-dichloro-2-propenyl)oxime, nD23.2 1.5658 (32) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (33) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl- oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, HD^^^ 1.5513 (34) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD26.0 1.5390 (35) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (36) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl- oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (37) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (38) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (39) 2-(2-ethyl-6-inethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (40) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (41) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (42) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (43) 6-(2-ethyl-6-inethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (44) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone 0-(3,3-dichloro-2-propenyl)oxime (45) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime (46) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime (47) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime, nD25.5 1.5408 (48) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime (49) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-acetone 0-(3,3-dichloro-2-propenyl)oxime (50) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl- oxyacetone 0-(3,3-dichloro-2-propenyl)oxime (51) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime (52) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime (53) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime (54) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone 0-(3,3-dichloro-2-propenyl)oxime (55) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetone 0-(3,3-dichloro-2-propenyl)oxiine (56) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime (57) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime (58) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetone 0-(3,3-dichloro-2-propenyl)oxiine (59) 3-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (60) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (61) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (62) 3-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (63) 3-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (64) 3-(2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- ethoxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (65) 3-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (66) 3-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (67) 3-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (68) 3-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (69) 3-(2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)ethoxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (70) 3-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (71) 3-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (72) 3-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (73) 3-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (74) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetal-dehyde 0-(3,3-dichloro-2-propenyl)oxime, nD22.3 1.5680 (75) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pionaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD22.3 1.5646 (76) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5509 (77) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-hyde 0-(3,3-dichloro-2-propenyl)oxime (78) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 0-(3,3-dichloro-2-propenyl)oxime (79) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (80) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal 0-(3,3-dichloro-2-propenyl)oxiine (81) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal O-(3,3-dichloro-2-propenyl)oxime (82) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal 0-(3,3-dichloro-2-propenyl)oxime (83) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (84) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-acetone 0-(3,3-dichloro-2-propenyl)oxime (85) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime (86) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butanal 0-(3,3-dichloro-2-propenyl)oxime (87) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentanal 0-(3,3-dichloro-2-propenyl)oxime (88) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexanal 0-(3,3-dichloro-2-propenyl)oxime (89) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde 0-tert-butyloxime (90) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetaldehyde 0-tert-butyloxime, nD25.6 1.5253 (91) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-tert-butyloxime, nD26.0 1.5181 (92) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy- acetaldehyde 0-tert-butyloxime (93) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetaldehyde 0-tert-butyloxime (94) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde O-tert-butyloxime (95) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde O-tert-butyloxime (96) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde O-tert-butyloxime (97) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetaldehyde O-tert-butyloxime (98) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde O-tert-butyloxime (99) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetaldehyde O-tert-butyloxime (100) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetaldehyde O-tert-butyloxime (101) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone O-tert-butyloxime (102) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone O-tert-butyloxime (103) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone O-tert-butyloxime, nD25.0 1.5170 (104) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone O-tert-butyloxime, nD25.5 1.5170 (105) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone O-tert-butyloxime (106) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy- acetone 0-tert-butyloxime (107) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone 0-tert-butyloxime (108) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-tert-butyloxime (109) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-tert-butyloxime (110) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone 0-tert-butyloxime (111) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone 0-tert-butyloxime (112) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetone 0-tert-butyloxime (113) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetone 0-tert-butyloxime (114) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetone 0-tert-butyloxime (115) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetone 0-tert-butyloxime (116) 3-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde 0-tert-butyloxime (117) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)propionaldehyde 0-tert-butyloxime (118) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)propionaldehyde 0-tert-butyloxime (119) 3-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)propionaldehyde 0-tert-butyloxime (120) 3-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)- hexyloxy)propionaldehyde 0-tert-butyloxime (121) 3-(2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde O-tert-butyloxime (122) 3-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propionaldehyde O-tert-butyloxime (123) 3-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)propionaldehyde O-tert-butyloxime (124) 3-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)propionaldehyde O-tert-butyloxime (125) 3-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex-yloxy)propionaldehyde O-tert-butyloxime (126) 3-(2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)ethoxy)propionaldehyde O-tert-butyloxime (127) 3-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyloxy)propionaldehyde O-tert-butyloxime (128) 3-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyloxy)propionaldehyde O-tert-butyloxime (129) 3-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxy)propionaldehyde O-tert-butyloxime (130) 3-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyloxy)propionaldehyde O-tert-butyloxime (131) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-hyde O-tert-butyloxime nD22.3 1.5371 (132) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone O-tert-butyloxime (133) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pionaldehyde O-tert-butyloxime, nD2433 1.5345 (134) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-tert-butyloxime,nD24.5 1.5237 (135) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde- hyde 0-tert-butyloxime (136) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone O-tert-butyloxime (137) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro- pionaldehyde 0-tert-butyloxime (138) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal 0-tert-butyloxime (139) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta- nal O-tert-butyloxime (140) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal 0-tert-butyloxime (141) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- acetaldehyde 0-tert-butyloxime (142) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- acetone 0-tert-butyloxime (143) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- ' propionaldehyde 0-tert-butyloxime (144) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- butanal 0-tert-butyloxime (145) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- pentanal 0-tert-butyloxime (146) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- hexanal 0-tert-butyloxime (147) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl- oxyacetaldehyde oxime, nD24.5 1.5278 (148) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde oxime, m.p., 62.8°C (149) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde oxime, nD21.2 1.5465 (150) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)aceto-phenone 0-(3,3-dichloro-2-propenyl)oxime, nD23.4 1.5929 (151) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)aceto-phenone 0-tert-butyloxime, nD23.4 1.5622 (152) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal oxime, nD23.4 1.5600 (153) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-isopropyloxime, nD23.0 1.5242 (154) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxycetaldehyde 0-sec-butyloxime, nD24.0 1.5211 (155) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-isobutyloxime, nD25.2 1.5206 (156) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-neopentyloxime, nD25.2 1.5106 (157) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(4-trifluoromethylbenzyl)oxime, nD24.8 1.5345 (158) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-methyloxime, nD24.7 1.5343 (159) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-ethyloxime, nD24.7 1.5291 (160) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-benzyloxime, nD24.7 1.5550 (161) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime, nD24.4h 1.5423 (162) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-phenyloxime, nD24.4 1.5613 (163) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-cyclohexyloxime, nD24.4 1.5289 (164) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(2,2,2-tribromoethyl)oxime, nD25.3 1.5671 (165) 5-(2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(2,2,2-trifluoroethyl)oxime, nD25.3 1.5058 (166) 4-(2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-isopropyloxime, nD25.3 1.5266 (167) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-isopropyloxime, nD25.3 1.5212 (168) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime, nD25.3 1.5445 (169) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime, nD25.3 1.5372 (170) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-isopropyloxime, nD25.3 1.5337 (171) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(2,2,2-trichloroethyl)oxime, nD25.3 1.5520 (172) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-phenyloxime, nD25.3 1.5725 (173) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-isopropyloxime, nD25.5 1.5208 (174) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(2,2,2-trichloroethyl)oxime, nD25.5 1.5378 (175) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-benzyloxime, nD25.5 1.5510 (176) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-ethyloxime, nD25.5 1.5262 (177) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-acetyloxime, nD25.6 1.5318 (178) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-pivaloyloxime, nD25.6 1.5195 (179) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(4-trifluoromethylbenzoyl)oxime, nD25.6 1.5300 (180) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N-tert-butylcarbamoyl)oxime, nD25.6 1,5191 (181) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N-phenylcarbamoyl)oxime, nD25.6 1.5546 (182) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(l,l,l,3,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4829 (183) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-bxyacetaldehyde 0-(l,l,l53,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4821 (184) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(l,l,l,3,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4807 (185) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(l,l,l,3,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4850 (186) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 0-(3-(5-trifluoromethyl-2-pyridyloxy)propyl)oxime, nD23.0 1.5310 (187) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-nal 0-isopropyloxime (188) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-isopropyloxime (189) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-nal 0-(2,2,2-trichloroethyl)oxime (190) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-(2,2,2-trichloroethyl)oxime (191) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-isopropyloxime (192) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-(2,2,2-trichloroethyl)oxime (193) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-isobutyloxime (194) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-isobutyloxime (195) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-sec-butyloxime (196) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-sec-butyloxime (197) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(2,2,2-tribromoethyl)oxime (198) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(2,2,2-tribromoethyl)oxime (199) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(2,2,2-trifluoroethyl)oxime (200) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(2,2,2-trifluoroethyl)oxime (201) 4-(2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)-2-bu-tenyloxyacetone 0-tert-butyloxime (202) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-2-bu-tynyloxyacetone 0-tert-butyloxime (203) 2-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)ethoxyacetone 0-tert-butyloxime, nD23.0 1.5172 (204) 2-(N-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethyl)-N-methylamino)ethoxyacetone 0-tert-butyloxime (205) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)cyclo-hexyloxyacetone 0-tert-butyloxime (206) 7-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)heptyl-oxyacetone 0-tert-butyloxime (207) l-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)-2-butanone 0-tert-butyloxime, HD^^^ 1.5140 (208) l-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)-3,3-dimethyl-2-butanone 0-tert-butyloxime, IID^^^ 1.5102 (209) 2-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)acetophenone 0-tert-butyloxime, nD23.4 1.5483 (210) 2-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)cyclohexanone 0-tert-butyloxime (211) 5-(2,6-dichloro-4-(3,3-dibromo-2-propenyloxy)phenoxy)pen-tyloxyacetone 0-tert-butyloxime (212) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-triphenylmethyloxime (213) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-cyanomethyloxime (214) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(tert-butoxycarbonylmethyl)oxime (215) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(2,2-diethoxyethyl)oxime (216) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(p-toluenesulfonyl)oxime (217) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N,N-diethylcarbamoyl)oxime (218) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N-tert-butylthiocarbamoyl)oxime (219) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde oxime (220) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetaldehyde oxime (221) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde oxime (222) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-acetaldehyde oxime (223) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetaldehyde oxime (224) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde oxime (225) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde oxime (226) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde oxime (227) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- propyloxyacetaldehyde oxime (228) 4-(2-ethyI-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde oxime (229) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetaldehyde oxime (230) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetaldehyde oxime (231) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)- ethoxyacetone oxime (232) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone oxime (233) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone oxime (234) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxy ace tone oxime, nD25.0 1.5460 (235) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone oxime (236) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-acetone oxime (237) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone oxime (238) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone oxime (239) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone oxime (240) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone oxime (241) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone oxime (242) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetone oxime (243) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetone oxime (244) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- pentyloxyacetone oxime (245) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- hexyloxyacetone oxime (246) 3-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde oxime (247) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)propionaldehyde oxime (248) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)propionaldehyde oxime (249) 3-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)propionaldehyde oxime (250) 3-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxy)propionaldehydeoxime (251) 3-(2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde oxime (252) 3-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propionaldehyde oxime (253) 3-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)propionaldehyde oxime (254) 3-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)propionaldehyde oxime (255) 3-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex-yloxy)propionaldehyde oxime (256) 3-(2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)ethoxy)propionaldehyde oxime (257) 3-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyloxy)propionaldehyde oxime (258) 3-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyloxy)propionaldehyde oxime (259) 3-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxy)propionaldehyde oxime (260) 3-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyloxy)propionaldehyde oxime (261) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-hyde oxime (262) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone oxime (263) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro- pionaldehyde oxime (264) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta- nal oxime (265) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa- nal oxime (266) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde- hyde oxime (267) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone oxime (268) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro- pionaldehyde oxime (269) 4-(2,6-diethyl-4-(3,3-dichlorO-2-propenyloxy)phenoxy)butanal oxime (270) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta- nal oxime (271) 6-(2,6-diethyl-4-(3,3-dichlorO-2-propenyloxy)phenoxy)hexanal oxime (272) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- acetaldehyde oxime (273) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- acetone oxime (274) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propionaldehyde oxime (275) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butanal oxime (276) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentanal oxime (277) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexanal oxime (278) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)aceto-phenone oxime (279) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 76.2°C (280) 4-(2,6-dichloro-4-(3,3-dibromo-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 88.2°C (281) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 88.0°C (282) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-(3,3-dibromo-2-propenyl)oxime, m.p., 90.8°C (283) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro- ^ pyloxy)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5872 (284) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5852 (285) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5819 (286) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5941 (287) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-ethyloxime, nD21.5 1.5760 (288) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-ethyloxime, nD21.5 1.5664 (289) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-ethyloxime, nD21.5 1,5613 (290) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-tert-butyloxime, nD21.5 1.5628 (291) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-tert-butyloxime, nD21.5 1.5588 (292) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-tert-butyloxime, nD21.5 1.5528 (293) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-ethyloxime, nD24.5 1.5948 (294) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-tert-butyloxime, nD24.5 1.5949 (295) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5950 (296) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5943 (297) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-ethyloxime, m.p., 41.9°C (298) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-tert-butyloxime, m.p., 56.4° C (299) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5785 (300) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5909 (301) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-methyloxime, nD24.5 1.5802 (302) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde O-methyloxime nD24.5 1.5756 (303) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-ethyloxime, m.p., 42.6°C (304) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-ethyloxime nD24.5 1.5723 (305) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde O-methyloxime, nD24.5 1.5871 (306) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde O-methyloxime, m.p,, 63.5°C (307) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone O-methyloxime, nD25.5 1.5642 (308) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-propyloxime, nD22.5 1.5733 (309) 4'-(4-(2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone O-methyloxime, nD22.5 1.5686 (310) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-propyloxime, nD22.5 1.5589 (311) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde O-methyloxime, m.p., 95.9°C (312) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-(2-propenyl)oxime, m.p., 75.6°C (313) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-benzyloxime, m.p., 70.3°C (314) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-tert-butyloxime, nD24.5 1.5713 (315) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-iso-propyloxime, nD24.5 1.5643 (316) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde O-isobutyloxime, nD24.5 1.5571 (317) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzophenone 0-ethyloxime, nD24.5 1.5943 (318) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propiophenone O-ethyloxime, m.p., 42.4°C (319) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)valerophenone O-ethyloxime, nD24.5 1.5535 (320) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde O-ethyloxime, nD24.5 1.5730 (321) 4'-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)acetophenone O-ethyloxime, m.p., 56.1°C (322) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yloxy)acetophenone O-ethyloxime, nD24.5 1.5840 (323) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.01.6006 (324) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-benzyloxime, nD22.5 1.6095 (325) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-tert-butyloxime, nD23.0 1.5753 (326) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde O-ethyloxime, m.p., 84.8°C (327) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-propyloxime, m.p., 45.4°C (328) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-isopropyloxime, nD24.0 1.5858 (329) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-sec-butyloxime, m.p., 59.6°C (330) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-allyl oxime, m.p., 63.9°C (331) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-sec-butyloxime, nD24.5 1,5783 (332) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propiophenone oxime, m.p., 140.0°C (333) 4-(5-(2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde oxime, m.p,, 90,1°C (334) 4'-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)acetophenone oxime, m.p., 79.5°C (335) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde oxime, nD24.0 1.5640 (336) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)valerophenone oxime, m.p., 87.0°C (337) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)acetophenone oxime, m.p., 121.0°C (338) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-propyloxime, IID^^^ 1.5703 (339) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-isopropyloxime, nD24.5 1.5653 (340) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-sec-butyloxime, nD24.5 1.5665 (341) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-iso-butyloxime, nD24.5 1.5579 (342) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-allyloxime, nD24.5 1.5990 (343) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-benzyloxime, nD24.5 1.5886 (344) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-(3,3-dichloro-2-propenyl)oxime, nD25.0 1.5965 (345) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-methyloxime, nD26.5 1.5947 (346) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth- yl)acetophenone 0-propyloxime, nD26.0 1.5808 (347) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth- yl)acetophenone O-propyloxime, nD26.0 1.5904 (348) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-tert-butyloxime, nD25.5 1.5717 (349) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-ethyloxime, nD26.0 1.5865 (350) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-benzyloxime, nD25.5 1.6655 (351) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde O-methyloxime, nD24.5 1,5921 (352) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-ethyloxime, nD24.5 1.5846 (353) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde O-propyloxime, nD24.5 1.5773 (354) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-iso-propyloxime, nD24.5 1,5762 (355) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-sec-butyloxime, nD25.0 1.5718 (356) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-tert-butyloxime, nD26.0 1,5669 (357) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-allyl oxime, nD26.0 1.5849 (358) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phonoxy)eth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD26.5 1.5932 (359) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)ph yl)benzaldehyde 0-benzyloxime, nD27.0 1.5967 (360) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)ph( noxy methyl)phenoxy)acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 87!) C (361) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phen(oxy)( th-yl)benzaldehyde 0-(4-tert-butylbenzyl)oxime, nD26.0 1.5818 (362) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)(th-yl)benzaldehyde 0-cyclohexyloxime, nD26.0 1.5685 (363) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-(3-phenylpropyl)oxime, nD26.0 1.5902 (364) 5-(l-(N.ethoxyimino)ethyl)-2-(3-(2,6-dichloro-4-(3,3-(li(:hl()r()-2-propenyloxy)phenoxy)propyloxy)pyridine, nD24.5 1.5701 (365) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)pr()-pyl)benzaldehyde 0-methyloxime, nD25.5 1.5876 (366) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)pro)-pyl)benzaldehyde 0-ethyloxime, nD26.0 1.5802 (367) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phcn()xy)pr()-pyl)benzaldehyde 0-propyloxime, nD25.5 1.5763 (368) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phoni)xy)pro-pyl)benzaldehyde 0-iso-propyloxime, nD25.5 1.5734 (369) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)ph(n()xy)pr()-pyl)benzaldehyde 0-tert-butyloxime, nD25.5 1.5673 (370) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)pr()- pyl)benzaldehyde 0-allyl oxime, nD25.5 1.5844 (371) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)pr()- pyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD25.0- 1.5920 (372) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)acetophenone 0-iso-propyloxime (373) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)acetophenone 0-butyloxime (374) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- yl)acetophenone 0-iso-butyloxime (375) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)acetophenone 0-sec-butyloxime (376) 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- yl)benzaldehyde O-butyloxime (377) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- yl)benzaldehyde O-methyloxime (378) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- yl)benzaldehyde 0-ethyloxime (379) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)benzaldehyde 0-propyloxime (380) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)benzaldehyde 0-iso-propyloxime (381) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)benzaldehyde 0-iso-butyloxime (382) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)benzaldehyde 0-iso-butyloxime (383) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)prO-pyl)benzaldehyde 0-sec-butyloxime (384) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime (385) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde O-methyloxime (386) 4-(4-(2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyl)benzaldehyde 0-ethyloxime (387) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyl)benzaldehyde 0-propyloxime (388) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyl)benzaldehyde 0-iso-propyloxime (389) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyl)benzaldehyde 0-butyloxime (390) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-iso-butyloxime (391) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bU-tyl)benzaldehyde 0-sec-butyloxime (392) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-tert-butyloxime (393) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone 0-(3,3-dichloro-2-propenyl)oxiine (394) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone 0-methyloxime (395) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ineth-yl)-2,2,2-trifluoroacetophenone 0-ethyloxime (396) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone 0-propyloxime (397) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone 0-iso-propyloxime (398) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth yl)-2,2,2-trifluoroacetophenone 0-butyloxime (399) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth yl)-2,2,2-trifluoroacetophenone 0-iso-butyloxime (400) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-l)-2,2,2-trifluoroacetophenone O-sec-butyloxiiiie (401) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone O-tert-butyloxiine (402) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone O-(3,3-dichloro-2-propenyl)oxime (403) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone O-methyloxime (404) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-ethyloxime (405) 4'-(2-(2,6-dichloro-4-(3,3-dicliloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-propyloxime (406) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-iso-propyloxime (407) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-butyloxime (408) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-iso-butyloxime (409) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-sec-butyloxime (410) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-tert-butyloxime (411) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-(3,3-dichloro-2-propenyl)oxime (412) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro pyl)-2,2,2-trifluoroacetophenone 0-methyloxime (413) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro pyl)-2,2,2-trifluoroacetophenone O-ethyloxime (414) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-propyloxime (415) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-iso-propyloxime (416) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-butyloxime (417) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-iso-butyloxime (418) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-sec-butyloxime (419) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone O-tert-butyloxime (420) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-methyloxime (421) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-propyloxime (422) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-iso-propyloxime (423) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-butyloxime (424) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-iso-butyloxime (425) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-sec-butyloxime (426) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-butyloxime (427) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu tyloxy)benzaldehyde 0-propyloxime (428) 4-(4-(2,6-dichloro-4-(3,3-dichloro-3-propenyloxy)phenoxy)bu tyloxy)benzaldehyde O-sec-butyloxime (429) 4-(4-(2,6-dichloro-4-(3,3-dichloro-4-propenyloxy)phenoxy)bu tyloxy)benzaldehyde 0-butyloxime (430) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-methyloxime (431) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen tyloxy)benzaldehyde 0-propyloxime (432) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-iso-propyloxime (433) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-butyloxime (434) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-iso-butyloxime (435) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen' tyloxy)benzaldehyde O-sec-butyloxime (436) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-tert-butyloxime (437) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde 0-methyloxime (438) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde 0-ethyloxime (439) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde 0-propyloxime (440) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde 0-iso-propyloxime (441) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-butyloxime (442) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-iso-butyloxime (443) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-sec-butyloxime (444) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-tert-butyloxime (445) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (446) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde O-methyloxime (447) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-ethyloxime (448) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde O-propyloxime (449) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-iso-propyloxime (450) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-butyloxime (451) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-iso-butyloxime (452) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-sec-butyloxime (453) (2-(4-(2,6'dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-tert-butyloxime (454) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime (455) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone O-methyloxime (456) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-ethyloxime (457) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-propyloxime (458) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-iso-propyloxime (459) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-butyloxime (460) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-iso-butyloxime (461) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-sec-butyloxime (462) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-tert-butyloxime (463) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-(3,3-dichloro-2-propenyl)oxime (464) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-methyloxime (465) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyloxy)-5-pyridyl phenyl ketone 0-ethyloxime ■^ (466) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-propyloxime (467) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-iso-propyloxime (468) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-butyloxime (469) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-iso-butyloxime (470) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-sec-butyloxime (471) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-tert-butyloxime (472) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-(3,3-dichloro-2-propenyl)oxime (473) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-methyloxime (474) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-ethyloxime (475) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-propyloxime (476) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-iso-propyloxime (477) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-butyloxime (478) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-iso-butyloxime (479) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-sec-butyloxime (480) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-tert-butyloxime (481) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-(3,3-dichloro-2-propenyl)oxime, m.p., GS.O'^C (482) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-methyloxime (483) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-ethyloxime (484) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde O-propyloxime (485) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde O-iso-propyloxiine (486) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ineth-yl)-2-thiophenecarboxaldehyde 0-butyloxime (487) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-iso-butyloxime (488) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-sec-butyloxime (489) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-tert-butyloxime (490) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)nieth-yl)-2-thiophenecarboxaldehyde 0-(3,3-dichloro-2-propenyl)oxime (491) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde O-methyloxime (492) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-ethyloxime (493) 5-((2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-propyloxime (494) 5-((2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-iso-propyloxime (495) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-butyloxime (496) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-iso-butyloxime (497) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-sec-butyloxime (498) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-tert-butyloxime (499) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde O-(3,3-dichloro-2-propenyl)oxinie (500) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural O-(3,3-dibroino-2-propenyl)oxime (501) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-methyloxime, nD26.0 1.5816 (502) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-ethyloxime, nD26.0 1.5772 (503) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-propyloxime, nD28.0 1.5732 (504) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-tert-butyloxime, nD27.5 1,5559 (505) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-allyloxime, nD25.5 1.5828 (506) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-(3,3-dichloro-2-propenyl)oxime, nD25.0 1.5906 (507) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-methyloxime, nnD26.5 1.5802 (508) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-ethyloxime, nD25.5 1.5744 (509) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-propyloxime, nD26.5 1.5708 (510) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-tert-butyloxime, nD26.5 1.5624 (511) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-allyloxime, nD26.5 1.5794 (512) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD26.5 1.5856 (513) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-methyloxime, nD25.5 1.5786 (514) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-ethyloxime, nD26.5 1.5717 (515) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-propyloxime, nD25.5 1.5692 (516) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-isopropyloxime, nD25.5 1.5656 (517) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-sec-butyloxime, nD26.5 1.5606 (518) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone O-tert-butyloxime, nD25.5 1.5580 (519) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-2,2,2-trifluoroacetophenone oxime (520) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-2,2,2-trifluoroacetophenone O-ethyloxime (521) 4'-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxy)acetophenone O-ethyloxime (522) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-(l,l,l,3,3,3-hexafluoroisopropyl)oxime (523) benzaldehydeO-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl. oxy)phenoxy)propyl)oxime, nD22.5 1.5797 (524) 4-(trifluoromethyl)benzaldehyde O-(3-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)propyl)oxime, nD22.5 1.5462 (525) acetaldehyde 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl oxy)phenoxy)propyl)oxime nD22.5 1.5437 (526) butanal O-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyl)oxime, nD22.5 1.5361 (527) trimethylacetaldehyde 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime,nD22.5 1.5262 (528) 4'-(trifluoromethyl)acetophenone O'(3-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)propyl)oxime, nD21.0 1.5433 (529) 4-(trifluoromethyl)benzaldehyde O-(4.(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime, nD21.0 1.5387 (530) trimethylacetaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxmne, nD21.5 1.5280 (531) 4'-(trifluoromethyl)acetophenone O-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime, nD21.5 1,5420 (532) acetaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime, nD21.5 1.5423 (533) benzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime, nD21.5 1.5731 (534) butanal O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyl)oxime, nD21.5 1.5332 (535) 4-chlorobenzaldehyde 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime, nD21.5 1.5850 (536) 4-chlorobenzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD21.5 1.5740 (537) 4-(trifluoromethyl)benzaldehyde O-(5-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime, nD20.5 1.5455 (538) 4'-(trifluoromethyl)acetophenone 0-(5-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime, nD20.5 1.5421 (539) benzaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime, nnD20.5 1.5756 (540) 4-chlorobenzaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2 propenyloxy)phenoxy)pentyl)oxime, nD20.5 1.5766 (541) acetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl oxy)phenoxy)pentyl)oxime, nD22.5 1.5391 (542) butanal O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe noxy)pentyl)oxime, nD22.5 1.5319 (543) hexanal O-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe noxy)propyl)oxime, nD22.5 1.5313 (544) hexanal O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyl)oxime, nD22.5 1.5288 (545) trimethylacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2 propenyloxy)phenoxy)pentyl)oxime, nD23.0 1,5178 (546) hexanal 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy) phenoxy)pentyl)oxime, nD23.0 1.5250 (547) 4'-(trifluoromethyl)acetophenone 0-(6-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)hexyl)oxime, nD20.5 1.5391 (548) 4-(trifluoromethyl)benzaldehyde O-(6-(2,6-dichloro-4-(3,3-di chloro-2-propenyloxy)phenoxy)hexyl)oxime, nD20.5 1.5412 (549) 4'-(trifluoromethyl)acetophenone O-(2-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)ethyl)oxime, nD23.5 1.5468 (550) 4-(trifluoromethyl)benzaldehyde O-(2-(2,6-dichloro-4-(3,3-di chloro-2-propenyloxy)phenoxy)ethyl)oxime, m.p., 79.8°C (551) hexanal 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe noxy)hexyl)oxime, nD21.0 1.5238 (552) nonanal O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe noxy)pentyl)oxime, nD22.0 1.5189 (553) dodecylaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propen-yloxy)phenoxy)pentyl)oxime, nD22.0 1.5110 (554) nonanal 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyl)oxime, nD22.0 1.5166 (555) dodecylaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propen-yloxy)phenoxy)butyl)oxime, nD22.0 1,5100 (556) hexanalO-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe- noxy)ethyl)oxime, nD21.5 1.5351 (557) butanal O-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe- noxy)ethyl)oxime, nD21.5 1,5410 (558) butanal O-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyl)oxime, nD23.0 1.5295 (559) 3,3-dimethyl-2-butanone O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD24.5 1.5233 (560) acetone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)oxime, nD24.5 1,5350 (561) 2-ethylbutanalO-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime, nD24.5 1.5235 (562) 3,3-dimethyl-2-butanone O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD22.0 1.5277 (563) 4-methyl-2-pentanone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD24.5 1.5265 (564) 4-methyl-2-pentanone 0-(5-(2,6-dichloro.4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD24.5 1.5230 (565) n-butyloxyacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD25.5 1.5240 (566) cyclohexanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl oxy)phenoxy)pentyl)oxime, nD25.5 1.5440 (567) chloroacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime, nD25.0 1.5451 (568) 6-chloro-3-pyridyl methyl ketone 0-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime, m.p., 79.5°C (569) 6-chloro-3-pyridyl methyl ketone 0-(5-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime, m.p,, 67.7°C (570) cyclohexanone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl' oxy)phenoxy)butyl)oxime, nD24.5 1.5470 (571) tetrahydrothiopyran-4-one 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD24.5 1.5650 (572) tetrahydrothiopyran-4-one 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD24.0 1.5612 (573) tetrahydro-4H-pyran-4-one O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime nD24.0 1.5459 (574) tetrahydro-4H-pyran-4-One 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD24.0 1.5440 (575) tetrahydrothiopyran-4-one 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD24.0 1.5541 (576) tetrahydro-4H-pyran-4-one O-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD24.0 1.5383 (577) 4-isopropylbenzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD24.0 1.5665 (578) 4-nitrobenzaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime, m.p., 76.4°C (579) 4-isopropoxybenzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD24.0 1.5701 (580) 3-methyl-2-butanone O-(3-(2,6-dichloro-4-(3,3-dichloro-2.pro penyloxy)phenoxy)propyl)oxime, nD24.0 1.5330 (581) 3-methyl-2-butanone O-(4-(2,6-dichlorO-4-(3,3-dichloro-2-prO-penyloxy)phenoxy)butyl)oxime, nD24.0 1.5302 (582) 3-methyl-2-butanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-pro penyloxy)phenoxy)pentyl)oxime, nD24.5 1.5280 (583) 3-methyl-2-butanone O-(6-(2,6-dichloro-4-(3,3-dichloro-2-pro penyloxy)phenoxy)hexyl)oxime, nD24.5 1.5255 (584) 3-methyl-l-butanalO-(3-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime, nD24.5 1.5296 (585) trimethylacetaldehyde 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD23.0 1.5220 (586) 3,3-dimethyl-2-butanone O-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime, nD23.0 1.5281 (587) 3,3-dimethyl-2-butanoneO-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD23.0 1.5230 (588) 4-methyl-2-pentanone 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime, nD23.0 1.5295 (589) 4-methyl-2-pentanone 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD23.0 1.5203 (590) 4,4-dimethyl-2-pentanone 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime, nD23.0 1.5277 (591) 4,4-dimethyl-2-pentanone O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD23.0 1.5259 (592) 4,4-dimethyl-2-pentanone O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD23.0 1.5205 (593) 4,4-dimethyl-2-pentanone O-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD23.0 1.5212 (594) 2-furaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl oxy)phenoxy)butyl)oxime, nD23.0 1.5690 (595) 2-thiophenecarbaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2 propenyloxy)phenoxy)butyl)oxime, nD23.0 1.5857 (596) 3-thiophenecarbaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD22.5. 1.5859 (597) l-methyl-2-pyrrolecarbaldehyde O-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime, nD22.5 1.5802 (598) acetophenone 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyl)oxime (599) acetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime (600) acetophenone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime (601) 4'-chloroacetophenone 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime (602) 4'-chloroacetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (603) 4'-chloroacetophenone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (604) benzaldehyde O-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyl)oxime (605) benzaldehyde 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyl oxy)phenoxy)butyl)oxime (606) benzaldehyde 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime (607) 4-chlorobenzaldehydeO-(3-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime (608) 4-chlorobenzaldehydeO-(4-(2,6-diethyl-4-(3,3-dichloro-2-pro penyloxy)phenoxy)butyl)oxime (609) 4-chlorobenzaldehyde O-(5-(2,6-diethyl-4-(3,3-dichloro-2-pro penyloxy)phenoxy)pentyl)oxime (610) 4-(trifluoromethyl)benzaldehyde 0-(3-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)propyl)oxime (611) 4-(trifluoromethyl)benzaldehyde 0-(4-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime (612) 4-(trifluoromethyl)benzaldehydeO-(5-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime (613) acetophenone 0-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyl)oxime (614) acetophenone 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime (615) acetophenone 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime (616) 4'-chloroacetophenone O-(3-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime (617) 4'-chloroacetophenoneO-(4-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime (618) 4'-chloroacetophenone O-(5-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime (619) 4'-(trifluoromethyl)acetophenone O-(3-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)propyl)oxime (620) 4'-(trifluoromethyl)acetophenone 0-(4-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime (621) 4'-(trifluoromethyl)acetophenoneO-(5-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime (622) hexanalO-(4-(2,6-diethyl-4-(3,3-dichloro-2.propenyloxy)phe-noxy)butyl)oxime (623) hexanal O-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)oxime (624) trimethylacetaldehyde 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (625) trimethylacetaldehyde 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (626) 4-methyl-2-pentanone 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (627) 4-methyl-2-pentanone 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (628) 3,3-dimethyl-2-butanone O-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (629) 3,3-dimethyl-2-butanoneO-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (630) 3-methyl-2-butanone O-(4-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime (631) 3-methyl-2-butanone O-(5-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime (632) benzaldehydeO-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime (633) benzaldehyde 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime (634) benzaldehyde 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime (635) 4-chlorobenzaldehydeO-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime (636) 4-chlorobenzaldehydeO-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (637) 4-chlorobenzaldehyde O-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (638) 4-(trifluoromethyl)benzaldehyde 0-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime (639) 4-(trifluoromethyl)benzaldehyde 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (640) 4-(trifluoromethyl)benzaldehyde 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxiine (641) acetophenone 0-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime (642) acetophenone 0-(4-(2-ethyl-6-niethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime (643) acetophenone 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime (644) 4'-chloroacetophenoneO-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime (645) 4'-chloroacetophenone 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (646) 4'-chloroacetophenone 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (647) 4'-(trifluoromethyl)acetophenone 0-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime (648) 4'-(trifluoromethyl)acetophenone 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (649) 4'-(trifluoromethyl)acetophenone 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (650) hexanal 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime (651) hexanal 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime (652) trimethylacetaldehyde 0-(4-(2-ethyl-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxime (653) trimethylacetaldehyde 0-(5-(2-ethyl-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime (654) 4-methyl-2-pentanoneO-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (655) 4-methyl-2-pentanoneO-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (656) 3,3-dimethyl-2-butanone 0-(4-(2-ethyl-6-methyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime (657) 3,3-dimethyl-2-butanone 0-(5-(2-ethyl-6-methyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime (658) 3-methyl-2-butanone O-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (659) 3-methyl-2-butanone 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (660) benzaldehyde 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime (661) benzaldehyde 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro- - penyloxy)phenoxy)butyl)oxime (662) benzaldehyde 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime (663) 4-chlorobenzaldehyde O-(3-(2-chloro-6-inethyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)propyl)oxime (664) 4-chlorobenzaldehyde 0-(4-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxime (665) 4-chlorobenzaldehyde 0-(5-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime (666) 4-(trifluoromethyl)benzaldehyde 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime (667) 4-(trifluoromethyl)benzaldehyde 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (668) 4-(trifluoromethyl)benzaldehyde 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (669) acetophenone 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime (670) acetophenone 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro- ' penyloxy)phenoxy)butyl)oxime (671) acetophenone 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime (672) 4'-chloroacetophenone 0-(3-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)propyl)oxime (673) 4'-chloroacetophenone O-(4-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxime (674) 4'-chloroacetophenone 0-(5-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime (675) 4'-(trifluoromethyl)acetophenone 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime (676) 4'-(trifluoromethyl)acetophenone 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (677) 4'-(trifluoromethyl)acetophenone 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (678) hexanal O-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyl oxy)phenoxy)butyl)oxime (679) hexanal O-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime (680) trimethylacetaldehydeO-(4-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxiine (681) trimethylacetaldehyde O-(5-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime (682) 4-methyl-2-pentanone 0-(4-(2-chloro-6-inethyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxime (683) 4-methyl-2-pentanone O-(5-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime (684) 3,3-dimethyl-2-butanone 0-(4-(2-chloro-6-methyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime (685) 3,3-dimethyl-2-butanone 0-(5-(2-chloro-6-methyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime (686) 3-methyl-2-butanone 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime (687) 3-inethyl-2-butanone O-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime (688) methyl 3-pyridyl ketone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD19.5 1.5715 (689) methyl 2-pyridyl ketone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD19.5 1.5717 (690) 4-(N,N-dimethylamino)benzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, IND19.5 1.5817 (691) 4-cyanobenzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime, m.p., 71.2°C (692) 4'-nitroacetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime, nD19.0 1.5878 (693) 3'-nitroacetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxiine, nD19.0 1.5719 (694) 2'-nitroacetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime, nD20.5 1.5615 (695) methyl 4-pyridyl ketone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD20.5 1.5586 The following is a production example for the intermediate compounds of formula (12). Intermediate Production Example 1 Production of intermediate compound 2) First, 10.0 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 14,0 g of 1,3-dibromopropane, and 50 ml of N,N-dimethylformamide were placed in a reaction vessel, to which 5.3 g of potassium carbonate was added. After stirring at room temperature for 12 hours, the reaction mixture was filtered. The filtrate was poured into diluted hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate layer was washed twice with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 6.1 g (yield, 43%) of l-(3-bromopropyloxy)-2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)benzene. Then, 10.0 g of l-(3-bromopropyloxy)-2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)benzene obtained in the same manner as described above, 4.0 g of N-hydrox5rphthalimide, and 100 ml of N,N-dimethylformamide were placed in a reaction vessel, to which 3.4 g of potassium carbonate was added. After stirring at room temperature for 12 hours, the reaction mixture was poured into ice water, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was washed with hexane, which afforded 9.4 g (yield, 78.3%) of N-(3-(2,6-dichloro-4-(3,3-di- chloro-2-propenyloxy)phenoxy)propyloxy)phthalimide, m.p., 97.3°C. Then, 9.1 g of N-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenoxy)propyloxy)phthalimide was added to 150 ml of methanol, to which 1.9 g of hydrazine hydrate was added. The reaction mixture was stirred for 1 hour with heating under reflux, and returned to room temperature. To the reaction mixture was added 50 ml of water, from which the methanol was evaporated under reduced pressure. Further added were 15 ml of concentrated hydrochloric acid and 25 ml of water. The reaction mixture was stirred for 30 minutes with heating under reflux, returned to room temperature, and filtered. The crystals collected by filtration were added to 10% aqueous sodium hydrogencarbonate solution, and extracted with diethyl ether. The diethyl ether layer was washed with 10% aqueous sodium hydrogencarbonate solution and water. To this diethyl ether layer was added 3 ml of concentrated hydrochloric acid, and the mixture was concentrated and the dried, which afforded 6.8 g (yield, 92%) of 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)hydroxylamine hydrochloride, m.p., 171.8°C. Some specific examples of the intermediate compounds of formula (12) are shown below with their compound numbers and physical properties, if any. 1) 0-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth- V yl)hydroxylamine hydrochloride, m.p., 172.2°C 2) 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)hydroxylamine hydrochloride, m.p., 171.8°C 3) 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyl)hydroxylamine hydrochloride, m.p., 105,3°C 4) 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyl)hydroxylamine hydrochloride, m.p., 82.8°C 5) 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyl)hydroxylamine hydrochloride, m.p., 94.0°C 6) 0-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro- pyl)hydroxylamine hydrochloride 7) 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyl)hydroxylamine hydrochloride 8) 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyl)hydroxylamine hydrochloride 9) 0-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex-yl)hydroxylamine hydrochloride 10) 0-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyl)hydroxylamine hydrochloride 11) 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyl)hydroxylamine hydrochloride 12) 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)hydroxylamine hydrochloride 13) 0-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyl)hydroxylamine hydrochloride 14) 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyl)hydroxylamine hydrochloride 15) 0-(4-(2-chloro-6-methyl-4-(3,3-dichlorO-2-propenyloxy)phe-noxy)butyl)hydroxylamine hydrochloride 16) 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)hydroxylamine hydrochloride 17) 0-(6-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyl)hydroxylamine hydrochloride The following are production examples for the carbonyl compounds of formula (22) including the intermediate compounds of formula (13) or (14) in the present invention. Intermediate Production Example 2 Production of intermediate compound 18) First, 2.06 g of terephthalaldehyde and 20 ml of ethanol were placed in a reaction vessel, to which 0.15 g of sodium borohydride was slowly added with stirring under ice cooling. After stirring at room temperature for 12 hours, the ethanol was evaporated. The residue was poured into diluted hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate layer was washed twice with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 1.06 g (yield, 51%) of p-(hydroxy-methyl)benzaldehyde. To a mixture of 3.40 g of p-(hydroxymethyl)benzaldehyde obtained in the same manner as described above, 7,2 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 6.56 g of triphenylphosphine, and 50 ml of tetrahydro-furan was slowly added dropwise 5.05 g of diisopropyl azodicarboxylate with stirring under ice cooling. After stirring at room temperature for 12 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 4.75 g (yield, 46%) of 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyl)benzaldehyde, m.p., 93.9°C. Intermediate Production Example 3 Production of intermediate compound 23) First, 10.0 g of 2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenol, 14.0 g of 1,3-dibromopropane, and 50 ml of N,N-dimethylformamide were placed in a reaction vessel, to which 5.3 g of potassium carbonate was added. After stirring at room temperature for 12 hours, the reaction mixture was filtered. The filtrate was poured into diluted hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate layer was washed twice with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 6.1 g (yield, 43%) of l-(3-bromopropyloxy)-2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)benzene. Then, 1.50 g of l-(3-bromopropyloxy)-2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)benzene obtained in the same manner as described above, 0.50 g of p-hydroxyacetophenone, and 30 ml of N,N-dimethylformamide were placed in a reaction vessel, to which 0.56 g of potassium carbonate was added. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 1.51 g (yield, 89%) of 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyloxy)acetophenone, m.p., 73.6°C. Intermediate Production Example 4 Production of intermediate compound 35) A mixture of 15.67 g of 4-bromophenetyl alcohol, 6.88 g of 3,4-dihydro-2H-pyran, a catalytic amount of p-toluenesulfonic acid monohydrate, and 100 ml of tetrahydrofuran was stirred at room temperature for 24 hours. The reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure, which afforded 21.5 g (yield, 97%) of 4-(2-(2-tetrahydropyranyloxy)ethyl)-l-bromo-benzene, m.p., 93.9°C. A mixture of 11,3 g of 4-(2-(2-tetrahydropyranyloxy)ethyl)-l-bromo-benzene and 100 ml of tetrahydrofuran was cooled to -78°C, to which 25.9 ml of 1.56 M solution of n-butyl lithium in n-hexane was added dropwise over 15 minutes. After stirring at -78°C for 1 hour, 4.2 ml of N,N-dimethyl-formamide was added dropwise at the same temperature over 15 minutes. After further stirring at -78°C for 1 hour, 100 ml of saturated aqueous ammonium chloride solution was added, and the stirring was further continued until the reaction mixture came to room temperature. The reaction mixture was extracted twice with 200 ml of ethyl acetate, and the ethyl acetate layers were combined, washed three times with saturated aqueous ammonium chloride solution, and washed with saturated aqueous sodium chloride solution. The combined ethyl acetate layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give a residue. This residue was subjected to silica gel chromatography, which afforded 7.20 g (yield, 78%) of 4-(2-(2-tetrahydropyranyloxy)ethyl)-benzaldehyde, nS24.5 1.5311. A mixture of 6.50 g of 4-(2-(2-tetrahydropyranyloxy)ethyl)benzalde-hyde, 130 ml of acetone, and 110 ml of IM hydrochloric acid was stirred at room temperature for 24 hours. The reaction mixture was neutralized by the addition of saturated aqueous sodium hydrogencarbonate solution, and extracted twice with 200 ml of ethyl acetate. The ethyl acetate layers were combined, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give a residue. This residue was purified by silica gel chromatography, which 3.88 g (yield, 93%) of 4-(2-hydroxyethyl)benzaldehyde. 'H-NMR (CDCI3/TMS) 6 (ppm): 1.42-1.88 (6H, m), 2.99 (2H, t), 3.42-3.49 (1H, m), 3.60-3.74 (2H, m), 3.94-4.04 (1H, m), 4.58-4.60 (1H, m), 7.38-7.43 (2H, m), 7.79-7.84 (2H, m), 9.98 (1H, s) To a mixture of 3.88 g of 4-(2-hydroxyethyl)benzaldehyde, 6,7 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 100 ml of tetrahydrofuran, and 6.0 g of triphenylphosphine was added dropwise a solution of 4.7 g of diisopropyl azodicarboxylate dissolved in 20 ml of tetrahydrofuran at the ice temperature over 1 hour. After completion of the addition, the reaction mixture was stirred at room temperature for 24 hours, and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, which afforded 6.63 g (yield, 69%) of 4-(2-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde, m.p., 54.2°C. Intermediate Production Example 5 Production of intermediate compound 37) First, 11.1 g of l-(3-bromopropyloxy)-2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)benzene, 3.31 g of benzoic acid, and 50 ml of N,N-dimethyl-formamide were placed in a reaction vessel, to which 3.90 g of potassium carbonate was added. After stirring at room temperature for 24 hours, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. this crude product was subjected to silica gel chromatography, which afforded 11.6 g (yield, 95%) of 3,5-dichloro-4-(3-benzoyloxypropyloxy)-l-(3,3-dichloro-2-propenyloxy)benzene. This 11.6 g of 3,5-dichlorO-4-(3-benzoyloxypropyloxy)-l-(3,3-dichloro-2-propenyloxy)benzene, 15.2 g of 10% aqueous potassium hydroxide solution, and 300 ml of methanol were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was concentrated. The concentrate was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, 7.41 g (yield, 83%) of 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-l-propyl alcohol. Then, 2.00 g of 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)-l-propyl alcohol obtained in the same manner as described above and 20 ml of tert-butyl methyl ether were placed in a reaction vessel, to which 0.24 g of sodium hydride (60% in oil) was slowly added with stirring under ice cooling. After 10 minutes, 0.9 g of 5-acetyl-2-chloropyridine (which had been produced in Reference Production Example 1 as described below) was added, and the mixture was stirred at room temperature for 1 hour and further stirred in an oil bath at 80°C (internal temperature). After 5 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which 0.62 g (yield, 23%) of 5-acetyl-2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)pyridine, m.p., 90.5°C. Intermediate Production Example 6 Production of intermediate compound 52) To a mixture of 56.3 g of 1,4-butanediol and 400 ml of N,N-dimeth-ylformamide was slowly added 11.0 g of 60% sodium hydride (in oil) with stirring under ice cooling. After stirring at room temperature for 12 hours, 49.3 g of bromoacetaldehyde diethylacetal was added dropwise, and the stirring was further continued at 60°C for 8 hours. The reaction mixture was poured into ice water, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 21.6 g (yield, 41%) of 4-(2,2-diethoxyethoxy)butanol. To a mixture of 2.30 g of 4-(2,2-diethoxyethoxy)butanol, 2.94 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 2.94 g of triphenylphosphine, and 30 ml of tetrahydrofuran was slowly added dropwise 2.48 g of diisopro-pylazodicarboxylate with stirring in a stream of nitrogen gas under ice cooling. After stirring at room temperature for 24 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 4.48 g (yield, 73%) of 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene. Then, 1.81 g of 3,5-dichloro-l-(3,3-dichlorO-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene was added to a mixture of 10 ml of acetic acid and 1 ml of concentrated hydrochloric acid with stirring under ice cooling, and the stirring was further continued for 15 minutes. The reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, saturated aqueous sodium hydrogencarbonate solution, and saturated aqueous sodium chloride solution in this order, dried over anhydrous magnesium sulfate, and concentrated, which afforded 1.51 g (yield, 94%) of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde. 'H-NMR (CDCI3/TMS) 6 (ppm): 1.92 (4H, m), 3.65 (2H, t), 3,99 (2H, t), 4.09 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.84 (2H, s), 9.75 (1H, s) Intermediate Production Example 7 Production of intermediate compound 57) To a mixture of 16,0 g of 4-(2,2-diethoxyethoxy)butanol, 18.9 g of 2,6-diehtyl-4-benzoylox5T)henol (which had been produced according to the method as described in JP-A 8-337549/1996), 20.2 g of triphenylphosphine, and 200 ml of tetrahydrofuran was slowly added dropwise 17.0 g of diisopro-pyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen gas. After stirring at room temperature for 6 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 31.4 g (yield, 88%) of 3,5-diethyM-benzoyl-oxy-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene, nD24.8 1.5129. To a solution of 31.0 g of 3,5-diethyl-l-benzoyloxy-4-(4-(2,2-diethoxy-ethoxy)butyloxy)benzene dissolved in 100 ml of methanol was added a solution of 5,1 g of potassium hydroxide dissolved in 25 g of water. After stirring at room temperature for 1 hour, the reaction mixture was acidified by the addition of diluted hydrochloric acid, and concentrated. The residue was poured into water, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.60 g (yield, 94%) of 3,5-diethyl-4-(4-(2,2-diethoxyethoxy)butyloxy)phenol, nD25.0 1.4890. Then, 19.9 g of 3,5-diethyl-4-(4-(2,2-diethoxyethoxy)butyloxy)phenol, 9.20 g of 1,1,3-trichloro-l-propene, 9.15 g of potassium carbonate, and 200 ml of N,N-dimethylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium, and concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 25.4 g (yield, 91%) of 3,5-diethyl-l-(3,3-di-chloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene, nD26.0 1.4991. To a mixture of 9.27 g of 3,5-diethyl-l-(3,3-dichloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene, 25 ml of acetic acid, and 5 ml of water was added 1 ml of concentrated hydrochloric acid at room temperature. After stirring at room temperature for 30 minutes, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, aqueous sodium hydrogen-carbonate solution, and aqueous sodium chloride solution in this order, dried over anhydrous magnesium sulfate, and concentrated, which afforded 7.62 g (yield, 98%) of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde. 'H-NMR (CDCI3/TMS) 6 (ppm): 1.22 (6H, t), 1.88 (4H, m), 2.63 (4H, q), 3.63 (2H, t), 3.74 (2H, t), 4.09 (2H, s), 4.61 (2H, d), 6.14 (1H, t), 6.57 (2H, s), 9.75 (1H, s) Intermediate Production Example 8 Production of intermediate compound 68) First, 65.1 g of 1,5-pentanediol, 18.6 g of proparygyl chloride, 12.0 g of sodium hydroxide (powdery), 5.69 g of benzyltriethylammonium chloride, and 200 ml of tetrahydrofuran were placed in a reaction vessel, and reaction mixture was stirred for 4 hours with heating under reflux. The reaction mixture was filtered through Celite, and the filtrate was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 12.4 g (yield, 35%) of 5-(2-pro-pynyloxy)pentanol, nD26.3 1.4533. To a mixture of 2.35 g of 5-(2-propynyloxy)pentanol, 4.32 g of 2,6-di-chloro-4-(3,3-dichloro-2-propenyloxy)phenol, 4.33 g of triphenylphosphine, and 30 ml of tetrahydrofuran was slowly added dropwise 3.64 g of diisopro-pyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen gas. After stirring at room temperature for 24 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography which afforded 5.17 g (yield, 84%) of 3,5-dichloro-l-(3,3-di-chloro-2-propynyloxy)-4-(5-(2-propynyloxy)pentyloxy)benzene, nD25.5 1.5400. A mixture of 4.12 g of 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(2-propenyloxy)pentyloxy)benzene, 0.36 g of mercury (II) sulfate, 5 ml of 1% aqueous sulfuric acid solution, and 50 ml of tetrahydrofuran was stirred at 60°C for 1 hour. The reaction mixture was filtered through Celite, and the filtrate was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with diluted hydrochloric acid and water in this order, dried over magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 4.05 g (yield, 94%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone, ND25.5' 1.5350. Intermediate Production Example 9 Production of intermediate compound 99) First, 16.3 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 20,7 g of potassium carbonate, 11.8 g of ethyl 5-bromovalerate, and 200 ml of N,N-dimethylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was filtered. The filtrate was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which 18.9 g (yield, 80%) of ethyl 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)valerate, nD24.0 1.5331. To a mixture of 4.06 g of ethyl 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)valerate and 50 ml of toluene was added dropwise 10.27 ml of 0.95 mol/liter diisobutyl aluminum hydride (hexane solution) over 30 minutes with stirring at -70°C in a stream of nitrogen gas. After further stirring at -70°C for 1 hour, 50 ml of saturated aqueous ammonium chloride solution was added. The reaction mixture was returned to room temperature, and poured into50 ml of diluted hydrochloric acid, and extracted twice with toluene. The toluene layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 3.52 g (yield, 96%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal. 'H-NMR (CDCI3/TMS) 6 (ppm): 1.80-2.11 (4H, brs), 2.58 (2H, t), 3.99 (2H, t), 4.62 (2H, d), 6.13 (1H, t), 6.85 (2H, d), 9.81 (1H, s) Intermediate Production Example 10 Production of intermediate compound 96) First, 8.64 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 4.98 g of potassium carbonate, 3.36 g of chloroacetone, and 50 ml of N,N-di-methylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was filtered. The filtrate was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 10.12 g (yield, 98%) of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy-acetone, m.p., 83.8*C. Some specific examples of the carbonyl compounds of formula (22) including the intermediate compounds of formula (13) or (14) of the present invention are shown below with their compound numbers and their physical properties, if any. 18) 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- yl)benzaldehyde, m.p., 93.9°C 19) 4-((2,6-dichloro-4-(3,3-dibromo-2-propenyloxy)phenoxy)meth- yl)benzaldehyde 20) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)- ethoxy)benzaldehyde, m.p., 81.3°C 21) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde, m.p., 76.5°C 22) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde, m.p., 54.9°C 23) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone, m.p., 73.6°'C 24) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyloxy)acetophenone, glassy 25) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro- pyloxy)benzaldehyde, Nd24.5 1.5809 26) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyloxy)benzaldehyde, nD24.5 1.5770 27) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro- pyloxy)benzophenone nD24.5 1.5928 28) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propiophenone, m.p., 39.8°C 29) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)valerophenone, nD24.5 1.5703 V 30) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde, m.p., 41.4°C 31) 4'-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)- pentyloxy)acetophenone, m.p., 101.0°C 32) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth- yloxy)acetophenone, m.p., 100.1°C 33) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- yl)benzaldehyde 1H-NMR (CDCI3/TMS) 6 (ppm): 4.61 (2H, d), 5.06 (2H, s), 6.13 (1H, t), 6.89 (2H, s), 7.58 (1H, t), 7.86 (1H, dt), 7.87 (1H, dt), 8.05 (1H, t), 10.06 (1H, s) 34) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth- yl)acetophenone, m.p., 88.6°C 35) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth- yl)benzaldehyde, m.p., 54.2°C 36) 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- yl)phenoxyacetaldehyde 37) 5-acetyl-2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe- noxy)propyloxy)pyridine, m.p., 90.5°C 38) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)benzaldehyde, m.p., 61.0°C 39) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)but-yl)benzaldehyde 40) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone 41) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 42) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 43) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde 44) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 45) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 46) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyloxy)-5-pyridyl phenyl ketone 47) 5-((2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)meth- yl)-2-furfural 48) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- yl)-2-thiophenecarboxaldehyde 49) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth- yl)-2-pyrrolcarboxaldehyde 50) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)- ethoxyacetaldehyde 51) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl- oxyacetaldehyde ^H-NMR (CDCI3/TMS) 6 (ppm): 2.15 (2H, t), 3,83 (2H, t), 4.08 (2H, t), 4.12 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.84 (2H, s), 9.74 (1H, s) 52) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl oxyacetaldehyde 'H-NMR (CDCI3/TMS) 5 (ppm): 1.92 (4H, m), 3.65 (2H, t), 3.99 (2H, t), 4.09 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.84 (2H, s), 9.75 (1H, s) 53) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl- oxyacetaldehyde 'H-NMR (CDCI3/TMS) 6 (ppm): 1.59-1.77 (4H, brs), 1.86 (2H, brs), 3.58 (2H, t), 3.96 (2H, t), 4.07 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.83 (2H, s), 9.74 (1H, s) 54) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl- oxyacetaldehyde 'H-NMR (CDCI3/TMS) δ(ppm): 1.4-1.9 (8H, m), 3.55 (2H, t), 3.95 (2H, t), 4.06 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.83 (2H, s), 9.74 (1H, s) 55) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy- acetaldehyde 56) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl- oxyacetaldehyde 57) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl- oxyacetaldehyde ^H-NMR (CDCI3/TMS) 6 (ppm): 1.22 (6H, t), 1.88 (4H, m), 2.63 (4H, q), 3.63 (2H, t), 3.74 (2H, t), 4.09 (2H, s), 4.61 (2H, d), 6.14 (1H, t), 6.57 (2H, s), 9.75 (1H, s) 58) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl- oxyacetaldehyde 1H-NMR (CDCI3/TMS) 6 (ppm): 1.22 (6H, t), 1.60-1.82 (6H, brs), 2.63 (2H, q), 3.58 (2H, t), 3.71 (2H, t), 4.07 (2H, s), 4.61 (2H, d), 6.14 (1H, t), 6.57 (2H, s), 9.74 (1H, s) 59) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxyphenoxy)hexyl- oxyacetaldehyde 60) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde 61) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetaldehyde 62) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde 63) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetaldehyde 64) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetaldehyde 65) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone 66) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl- oxyacetone 67) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl- oxyacetone 68) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl- oxyacetone, nD25.5 1.5350 69) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl- oxyacetone 70) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy- acetone 71) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl- oxyacetone 72) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl- oxyacetone 73) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl- oxyacetone 74) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl- oxyacetone 75) 2-(2-ethyl-6-inethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- ethoxyacetone 76) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- propyloxyacetone 77) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- butyloxyacetone 78) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- pentyloxyacetone 79) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- hexyloxyacetone 80) 3-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)- ethoxy)propionaldehyde 81) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro- pyloxy)propionaldehyde 82) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu- tyloxy)propionaldehyde 83) 3-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen tyloxy)propionaldehyde 84) 3-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex yloxy)propionaldehyde 85) 3-(2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy) ethoxy)propionaldehyde 86) 3-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro pyloxy)propionaldehyde 87) 3-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu tyloxy)propionaldehyde 88) 3-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen tyloxy)propionaldehyde 89) 3-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex yloxy)propionaldehyde 90) 3-(2-(2-ethyl-6-inethyl-4-(3,3-dichloro-2-propenyloxy)phe noxy)ethoxy)propionaldehyde 91) 3-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe noxy)propyloxy)propionaldehyde 92) 3-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe noxy)butyloxy)propionaldehyde 93) 3-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe noxy)pentyloxy)propionaldehyde 94) 3-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe noxy)hexyloxy)propionaldehyde 95) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde- hyde 96) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone, m.p., 83.8°C 97) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro- pionaldehyde 1H-NMR (CDCI3/TMS) δ (ppm): 2.91 (2H, dt), 4.33 (2H, t), 4.59 (2H, d), 6.11 (1H, t), 6.85 (2H, s), 9.97 (1H, d) 98) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta- nal 1H-NMR (CDCI3/TMS) 6 (ppm): 2.14 (2H, tt), 2.80 (2H, t), 3.99 (2H, t), 4.58 (2H, d), 6.11 (1H, t), 6.83 (2H, s), 9.88 (1H, s) 99) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta- nal 'H-NMR (CDCI3/TMS) δ (ppm): 1.80-2.11 (4H, brs), 2.58 (2H, t), 3.99 (2H, t), 4.62 (2H, d), 6.13 (1H, t), 6.85 (2H, d), 9.81 (1H, s) 100) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa- nal 1H-NMR (CDCI3/TMS) 6 (ppm): 1.50-1.95 (6H, brs), 2.48 (2H, t), 3.95 (2H, t), 4.58 (2H, d), 6.11 (1H, t), 6.83 (2H, s), 9.79 (1H, s) 101) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde- hyde 102) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 103) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pionaldehyde 104) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal 105) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta- nal 106) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal 107) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- acetaldehyde 108) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- acetone 109) 3-(2-ethyl-6-methyl-4-(3,3-dichlorO-2-propenyloxy)phenoxy)- propionaldehyde 110) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- butanal 111) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- pentanal 112) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)- hexanal 113) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)aceto- phenone, m.p., 112.5°C 114) 7-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)heptyl-oxyacetone 115) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-2-bu-tenyloxyacetone 116) 2-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)ethoxyacetone 117) 2-(N-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethyl)-N-methylamino)ethoxyacetone 118) 4-(2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)cyclo-hexyloxyacetone The following are production examples for the intermediate compounds of formula (15). Intermediate Production Example 11 Production of intermediate compound 138) First, 0.56 g of 2,6-dichlorO-4-benzoyloxyphenol (which can be produced according to the method as described in JP-A 8-337549/1996), 0.30 g of potassium carbonate, 0.74 g of 5-(methanesulfonyloxy)pentyloxy-acetone 0-tert-butyloxime, and 10 ml of N,N-dimethylformamide are placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(benzoyloxy)phenoxy)pentyloxyacetone 0-tert-butyloxime. To a solution of 0.99 g of 5-(2,6-dichloro-4-(benzoyloxy)phenoxy)-pentyloxyacetone 0-tert-butyloxime dissolved in 7.5 ml of methanol is added a solution of 0.15 g of potassium hydroxide dissolved in 1.5 ml of water. After stirring at room temperature for 1 hour, the reaction mixture is acidified by the addition of diluted hydrochloric acid, and concentrated. Water is added to the residue, and the mixture is extracted twice with ethyl acetate. The ethyl acetate layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-di-chloro-4-hydroxyphenoxy)pentyloxyacetone 0-tert-butyloxime. Some specific examples of the intermediate compounds of formula (15) are shown below with their compound numbers and their physical properties, if any. 119) 4-(2,6-dichloro-4-hydroxyphenoxy)butanal 0-isopropyloxime 120) 5-(2,6-dichloro-4-hydroxyphenoxy)pentanal 0-isopropyloxime 121) 6-(2,6-dichloro-4-hydroxyphenoxy)hexanal 0-isopropyloxime 122) 4-(2,6-dichloro-4-hydroxyphenoxy)butanal O-tert-butyloxime 123) 5-(2,6-dichloro-4-hydroxyphenoxy)pentanal 0-tert-butyl-oxime 124) 6-(2,6-dichloro-4-hydroxyphenoxy)hexanal 0-tert-butyloxime 125) 4-(2,6-dichloro-4-hydroxyphenoxy)butanal 0-(2,2,2-trichloro-ethyl)oxime 126) 5-(2,6-dichloro-4-hydroxyphenoxy)pentanal 0-(2,2,2-trichlo-roethyl)oxime 127) 6-(2,6-dichloro-4-hydroxyphenoxy)hexanal 0-(2,2,2-trichloro-ethyl)oxime 128) 4-(2,6-dichloro-4-hydroxyphenoxy)butanalO-(3,3-dichloro-2-propenyl)oxime 129) 5-(2,6-dichloro-4-hydroxyphenoxy)pentanal O-(3,3-dichloro-2-propenyl)oxiine 130) 6-(2,6-dichloro-4-hydroxyphenoxy)hexanal 0-(3,3-dichloro-2-propenyl)oxime 131) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetaldehyde O-isopropyloxime 132) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetaldehyde O-isopropyloxime 133) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetone O-isopropyloxime 134) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetone O-isopropyloxime 135) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-tert-butyloxime 136) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-tert-butyloxime 137) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetone 0-tert-butyloxime 138) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetone 0-tert-butyloxime 139) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetaldehyde O- (2,2,2-trichloroethyl)oxime 140) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime 141) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetone 0-(2,2,2-trichloroethyl)oxime 142) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetone 0-(2,2,2-trichloroethyl)oxime 143) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime 144) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime 145) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetone 0-(3,3-di-chloro-2-propenyl)oxime 146) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime 147) 4-(2,6-dichloro-4-hydroxyphenoxymethyl)benzaldehyde 0-sec-butyloxime 148) 4-(2,6-dichloro-4-hydroxyphenoxymethyl)benzaldehyde 0-t-butyloxime 149) 4-(2-(2,6-dichloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-sec-butyloxime 150) 4-(2-(2,6-dichloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-allyloxime 151) 4-(2-(2,6-dichloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime 152) 4-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-n-propyloxime 153) 4-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-isopropyloxime 154) 4-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)benzaldehyde O-sec-butyloxime 155) 4-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-t-butyloxime 156) 4'-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)acetophe-none 0-ethyloxime 157) 4'-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)propiophe-none O-ethyloxime 158) 4'-(4-(2,6-dichloro-4-hydroxyphenoxy)butyloxy)acetophenone O-ethyloxime 159) 4'-(4-(2,6-dichloro-4-hydroxyphenoxy)butyloxy)acetophenone 0-n-propyloxime 160) 4-(4-(2,6-dichloro-4-hydroxyphenoxy)butyloxy)benzaldehyde 0-isopropyloxime 161) 4'-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)-2,2,2-trifluo-roacetophenone O-ethyloxime 162) 4-(trifluoromethyl)benzaldehyde 0-(4-(2,6-dichloro-4-hy-droxyphenoxy)butyl)oxime 163) 4'-(trifluoromethyl)acetophenone 0-(4-(2,6-dichloro-4-hy-droxyphenoxy)butyl)oxime 164) trimethylacetaldehyde 0-(5-(2,6-dichloro-4-hydroxyphe- noxy)pentyl)oxime 165) 3,3-dimethyl-2-butanone 0-(5-(2,6-dichloro-4-hydroxyphe-noxy)pentyl)oxime 166) 3,3-dimethyl-2-butanone 0-(4-(2,6-dichloro-4-hydroxyphe-noxy)butyl)oxime 167) 4-methyl-2-pentanone 0-(4-(2,6-dichloro-4-hydroxyphenoxy)-butyl)oxime 168) 4-methyl-2-pentanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)-pentyl)oxime 169) 3-methyl-2-butanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)-pentyl)oxime Reference Production Example 1 Production example for 5-acetyl-2-chloropyridine used in Intermediate Production Example 5 First, 15.45 g of 6-chloronicotinic acid and 100 ml of diethyl ether were placed in a reaction vessel, to which 131 ml of methyl lithium (1.5 M ether solution) was slowly added dropwise with stirring under ice cooling (internal temperature, O°C to -5°C). After completion of the addition, the reaction mixture was further stirred at room temperature for 24 hours, and concentrated. The residue was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concen-trated. This crude product was subjected to silica gel chromatography, which 13.11 g (yield, 86%) of 5-acetyl-2-chloropyridine. The following are production examples for the intermediate r compounds of formula (21) Reference Production Example 2 Production of 0-(3,3-dichloro-2-propenyl)hydroxylamine hydrochloride To a mixture of 44 g of N-hydroxyphthalimide, 39 g of potassium carbonate, and 400 ml of N,N-dimethylformamide was added 41 g of 1,1,3-trichloro-1-propene at room temperature. After stirring at room temperature for 12 hours, the reaction mixture was poured into diluted hydrochloric acid to cause the deposition of crystals. These crystals were collected by filtration, washed with water and hexane in this order, and dried under reduced pressure, which afforded 66 g (yield, 90%) of N-(3,3-dichloro-2-propenyloxy)phthalimide. To a mixture of 66 g of N-(3,3-dichloro-2-propenyloxy)phthalimide and 300 ml of chloroform was slowly added dropwise a mixture of 13 g of hydrazine hydrate and 17 ml of isopropyl alcohol at room temperature. After stirring 3 hours with heating under reflux, the reaction mixture was returned to room temperature, in which 100 ml of hexane was poured. The reaction mixture was filtered, and the filtrate was concentrated to give a residue, in which 100 ml of hexane was again poured. This hexane solution was again filtered, and hydrogen chloride gas was blown in the filtrate to cause the deposition of crystals. These crystals were collected by filtration, and dried under reduced pressure, which afforded 26 g (yield, 60%) of 0-(3,3-dichloro-2-propenyl)hydroxylamine hydrochloride. 'H-NMR (CDCl3-CD30D/TMS)(5(ppm): 4.76 (2H, s), 6.17 (1H, t) Reference Production Example 3 Production of 0-(3-(5-trifluoro-methyl-2-pyridyloxy)propyl)hydroxylamine To a mixture of 12.6 g of 1,3-propanediol and 100 ml of N,N-dimethyl-formamide was added in portions 3.30 g of 60% sodium hydride (in oil) at room temperature over 30 minutes with stirring in a stream of nitrogen gas. After further stirring at room temperature for 1 hour, a solution of 10.0 g of 2-chloro-5-trifluoromethylpyridine in 20 ml of N,N-dimethylformamide was added dropwise over 40 minutes. After further stirring at room temperature overnight, 100 ml of about 2 N diluted hydrochloric acid was added over 15 minutes to complete the reaction. The reaction mixture was extracted twice with 500 ml of toluene in total. The toluene layers were combined, washed with diluted hydrochloric acid and saturated aqueous sodium hydrogencarbonate solution in this order, dried over anhydrous magnesium sulfate, and concentrated to give 9.70 g of oil. This oil was dissolved with heating in 300 ml of hexane, followed by recrystallization, which afforded 5.3 g (yield, 44%) of 2-(3-hydroxypropyloxy)-5-trifluoromethylpyridine, m.p., 46.6°C. To a mixture of 20.0 g of 2-(3-hydroxypropyloxy)-5-trifluoromethyl-pyridine, 14.7 g of N-hydroxyphthalimide, 23.6 g of triphenylphosphine, and 200 ml of tetrahydrofuran was slowly added dropwise 20.0 g of diisopropyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen gas. After stirring at room temperature for 24 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 27.8 g (yield, 84%) of N-(3-(5-trifluoro-methyl-2-pyridyloxy)propyloxy)phthalimide, m.p., 97.6°C. To a mixture of 12,8 g of N-(3-(5-trifluoromethyl-2-pyridyloxy)propyl-oxy)phthalimide and 150 ml of chloroform was slowly added dropwise a mixture of 1.74 g of hydrazine hydrate and 1.5 ml of isopropyl alcohol at room temperature. After stirring for 3 hours with heating under reflux, the reaction mixture was returned to room temperature, in which 150 ml of hexane was poured. The reaction mixture was filtered through Celite, and the filtrate was concentrated to give a residue, in which 100 ml of hexane was again poured. This hexane solution was left stand in a refrigerator in 3 days. The deposited crystals were collected by filtration, and dried under reduced pressure, which afforded 7.0 g (yield, 85%) of 0-(3-(5-trifIuoro-methyl-2-pyridyloxy)propyl)hydroxylamine, nD24.0 1,4652. Reference Production Example 4 0-(2,2,2-trichloroethyl)hydroxyl- amine hydrochloride To a mixture of 2.99 g of 2,2,2-trichloroethanol, 2.15 g of 0-(2,4,6-tri-methylbenzenesulfonyl)hydroxylamine (which had been produced according to the method as described in Synthesis, 1-17 (1977)), and 20 ml of diethyl ether was slowly added 0.68 g of sodium ethoxide with stirring under ice cooling. After stirring at room temperature for 5 hours, the deposited precipitate was removed by Celite filtration, and hexane was added to the filtrate. This hexane solution was bubbled with a blow of hydrogen chloride gas at room temperature to case the deposition of crystals. These crystals were collected by filtration, and dried under reduced pressure, which afforded 1.18 g (yield, 59%) of 0-(2,2,2-trichloroethyl)hydroxylamine hydrochloride. ^H-NMR (CDCI3-CD3OD/TMS) 6 (ppm): 4.84 (2H, s) The following are production examples for the intermediate compounds of formula (20). Reference Production Example 7 Production of compound 170) First, 5.21 g of 1,5-pentanediol is placed in a reaction vessel, to which 0.22 g of 60% sodium hydride (in oil) is slowly added at room temperature with stirring in a stream of nitrogen gas. After stirring at room temperature until the evolution of hydrogen gas ceases, 0.75 g of chloroacetaldehyde 0-tert-butyloxime is added at room temperature, and the reaction mixture is slowly warmed to 50°C. After further stirring at 50°C for 3 hours, the reaction mixture is poured into water, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, diluted hydrochloric acid, and water in this order, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-hydroxypentyloxy-aldehyde 0-tert-butyloxime. Reference Production Example 8 Production of intermediate compound 171 First, 13.02 g of 1,5-pentanediol, 2.40 g of sodium hydroxide (powdery), 1.14 g of benzyltriethylammonium chloride, and 100 ml of tetra-hydrofuran were placed in a reaction vessel, to which 8.18 g of chloroacetone 0-tert-butyloxime was slowly added dropwise with stirring under heating under reflux. After further stirring for 8 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with diluted hydrochloric acid and water in this order, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 6.79 g (yield, 59%) of 5-hydroxy-pentyloxyacetone 0-tert-butyloxime, nD23.2 1.4493. Some specific examples of the intermediate compounds of formula (20) are shown below with their compound numbers and their physical properties, if any. 170) 5-hydroxypentyloxyacetaldehyde 0-tert-butyloxime 171) 5-hydroxypentyloxyacetone 0-tert-butyloxime 172) 4-hydroxybutyloxyacetone 0-tert-butyloxime 173) 4-hydroxy-2-butenyloxyacetone 0-tert-butyloxime 174) 4-hydroxy-2-butynyloxyacetone 0-tert-butyloxime 175) 2-(2-hydroxyethoxy)ethoxyacetone 0-tert-butyloxime, nD24.7 1.4451 176) 2-(N-2-hydroxyethyl-N-methylamino)ethoxyacetone 0-tert-butyloxime 177) 4-hydroxycyclohexyloxyacetone 0-tert-butyloxime 178) l-(5-hydroxypentyloxy)-2-butanone 0-tert-butyloxime, nD23.4 1.4479 179) l-(5-hydroxypentyloxy)pinacolone 0-tert-butyloxime, UD^^^ 1.4451 180) 2-(5-hydroxypentyloxy)acetophenone 0-tert-butyloxime, nD23.2 1.5090 181) 2-(5-hydroxypentyloxy)cyclohexanone 0-tert-butyloxime The following are production examples for the intermediate compounds of formula (19). The intermediate compounds produced in Reference Production Example 10 or 12 can also be used as the starting material in Reference Production Example 7, and the intermediate compounds produced in Reference Production Example 11 or 13 can also be used as the starting material in Reference Production Example 8. Reference Production Example 9 Production of intermediate compound 182) To 2.94 g of 40% aqueous chloroacetaldehyde solution was added 2.94 g of 0-(3,3-dichloro-2-propenyl)hydroxylamine hydrochloride with stirring at room temperature. After stirring at room temperature for 2 hours, the reaction mixture was extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 1.94 g (yield, 96%) of chloroacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD23.2 1.5038. Reference Example 10 Production of intermediate compound 183) To 9.81 g of 40% aqueous chloroacetaldehyde solution was added 3.77 g of 0-tert-butylhydroxylamine hydrochloride with stirring at room temperature. After stirring at room temperature for 2 hours, the reaction mixture was extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 4.21 g (yield, 94%) of chloroacetaldehyde 0-tert-butyloxime, UD23.2 1.4418. Reference Production Example 11 Production of intermediate compound 184) A mixture of 1.51 g of 0-tert-butylhydroxylamine hydrochloride, 0.93 g of chloroacetone, and 10 ml of diethyl ether is stirred at room temperature for 3 hours, poured into water, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords chloroacetone 0-tert-butyloxime, Reference Production Example 12 Production of intermediate compound 183) To 3.92 g of 40% aqueous chloroacetoaldehyde solution is 2.08 g of hydroxylamine hydrochloride with stirring at room temperature. After stirring at room temperature for 24 hours, the reaction mixture is extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords 1.32 g (yield, 71%) of chloroacetoaldehyde oxime. Then, 0.47 g of chloroacetoaldehyde oxime, 0.1 ml of concentrated sulfuric acid, and 10 ml of diethyl ether are placed in a reaction vessel, into which isobutene gas is blown with stirring under ice cooling, and the stirring is further continued at room temperature. After completion of the reaction, the reaction mixture is slowly poured into saturated aqueous sodium hydro-gencarbonate solution, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with 10% aqueous sodium hydroxide solution and water in this order, dried over anhydrous magnesium sulfate, and concentrated, which affords chloroacetoaldehyde 0-tert-butyloxime. Reference Production Example 13 Production of intermediate compound 184) A mixture of 0.83 g of hydroxylamine hydrochloride, 0.93 g of chloro- acetone, and 10 ml of diethyl ether is stirred at room temperature for 3 hours, poured into water, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords chloroacetone oxime. Then, 0.54 g of chloroacetone oxime, 0.1 ml of concentrated sulfuric acid, and 10 ml of diethyl ether are placed in a reaction vessel, into which isobutene gas is blown with stirring under ice cooling, and the reaction mixture is further stirred at room temperature. After completion of the reaction, the reaction mixture is slowly poured into saturated aqueous sodium hydrogencarbonate solution, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with 10% aqueous sodium hydroxide solution and water in this order, dried over anhydrous magnesium hydroxide, and concentrated, which affords chloroacetone 0-tert-butyloxy-oxime. Reference Production Example 14 Production of intermediate compound 189) First, 0.22 g of 5-hydroxypentyloxyaldehyde 0-tert-butyloxime, 0.12 g of triethylamine, and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which 0.14 g of methanesulfonyl chloride is slowly added dropwise with stirring under ice cooling. After completion of the addition, the reaction mixture is further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords 5-(methane-sulfonyloxy)pentyloxyaldehyde 0-tert-butyloxime. Reference Production Example 15 Production of intermediate compound 190) First, 0.23 g of 5-hydroxypentyloxyacetone 0-tert-butyloxime, 0.12 g of triethylamine, and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which 0.14 g of methanesulfonyl chloride is slowly added with stirring under ice cooling. After completion of the addition, the reaction mixture is further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords 5-(methanesulfonyloxy)pentyloxy-acetone 0-tert-butyloxime. Some specific examples of the intermediate compounds of formula (19) are shown below with their compound numbers and their physical properties, if any. Intermediate compounds 182) to 188) can also be sued as the starting materials for the production of intermediate compounds 170) to 181) of formula (19). 183) 184) 185) 186) 187) 188) 189) 182) chloroacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD 23.2 1.5038 chloroacetaldehyde 0-tert-butyloxime, nD23.2 1.4418 chloroacetone 0-tert-butyloxime l-bromo-2-butanone 0-tert-butyloxime 1-bromopinacolone 0-tert-butyloxime 2-chloroacetophenone 0-tert-butyloxime 2-chlorocyclohexanone 0-tert-butyloxime 5-(methanesulfonyloxy)pentyloxyacetaldehyde 0-tert-butyl oxime oxime 190) 5-(methanesulfonyloxy)pentyloxyacetone 0-tert-butyloxime 191) 4-(methanesulfonyloxy)butyloxyacetone 0-tert-butyloxime 192) 4-(methanesulfonyloxy)-2-butenyloxyacetone 0-tert-butyl 193) 4-(methanesulfonyloxy)-2-butynyloxyacetone 0-tert-butyl- oxime 194) 2-(2-(methanesulfonyloxy)ethoxy)ethoxyacetone 0-tert-butyl-oxime 195) 2-(N-2-(methanesulfonyloxy)ethyl-N-methylamino)ethoxy-acetone 0-tert-butyloxime 196) 4-(methanesulfonyloxy)cyclohexyloxyacetone 0-tert-butyloxime 197) l-(5-(methanesulfonyloxy)pentyloxy)-2-butanone 0-tert-butyloxime 198) l-(5-(methanesulfonyloxy)pentyloxy)pinacolone 0-tert-butyloxime 199) 2-(5-(methanesulfonyloxy)pentyloxy)acetophenone 0-tert-butyloxime 200) 2-(5-(methanesulfonyloxy)pentyloxy)cyclohexanone 0-tert-butyloxime The following are formulation examples in which -parts- are by weight and the present compounds are designated by their compound numbers as described above. Formulation Example 1 Emulsifiable concentrates First, 10 parts of each of the present compounds (1) to (687) is dissolved in 35 parts of xylene and 35 parts of N,N-dimethylformamide, to which 14 parts of polyoxyethylene styrylphenyl ether and 6 parts of calcium dodecylbenzenesulfonate are added. The mixture is well stirred to give a 10% emulsifiable concentrate of each compound. Formulation Example 2 Wettable powders First, 20 parts of each of the present compounds (1) to (687) is added to a mixture of 4 parts of sodium lauryl sulfate, 2 parts of calcium lignin sulfonate, 20 parts of synthetic hydrated silicon oxide fine powder, and 54 parts of diatomaceous earth. The mixture is stirred with a mixer to give a 20% wettable powder of each compound. Formulation Example 3 Granules To five parts of each of the present compounds (1) to (687) are added 5 parts of synthetic hydrated silicon oxide fine powder, 5 parts of sodium dodecylbenzenesulfonate, 30 parts of bentonite, and 55 parts of clay, and the mixture is well stirred. A suitable amount of water is added to the mixture, which is further stirred, granulated with a granulator, and air-dried to give a 5% granule of each compound. Formulation Example 4 Dusts First, 1 part of each of the present compounds (1) to (687) is dissolved in a suitable amount of acetone, to which 5 parts of synthetic hydrated silicon oxide fine powder, 0.3 part of PAP, and 93.7 parts of clay are added, and the mixture is stirred with a mixer. The removal of acetone by evaporation gives a 1% dust of each compound. Formulation Example 5 Flowables First, 20 parts of each of the present compounds (1) to (687) is mixed with 1.5 parts of sorbitan trioleate and 28.5 parts of an aqueous solution containing 2 parts of polyvinyl alcohol. The mixture is pulverized into fine particles having a particle size of not more than 3 µm with a sand grinder, to which 40 parts of an aqueous solution containing 0.05 part of xanthan gum and 0.1 part of aluminum magnesium silicate is added and then 10 parts of propylene glycol is added. The mixture is stirred to give a 20% flowable of each compound. Formulation Example 6 Oil sprays First, 0.1 part of each of the present compounds (1) to (687) is dissolved in 5 parts of xylene and 5 parts of trichloroethane. The solution is mixed with 89.9 parts nf deodorized kerosine to give a 0.1% oil spray of each compound. Formulation Example 7 Oil-based aerosols First, 0.1 part of each of the present compounds (1) to (687), 0.2 part of tetramethrin, 0.1 part of d-phenothrin, and 10 parts of trichloroethane are dissolved in 59.6 parts of deodorized kerosine, and the solution is put in an aerosol vessel. The vessel is equipped with a valve, through which 30 parts of a propellant (liquefied petroleum gas) is charged under increased pressure to give an oil-based aerosol of each compound. Formulation Example 8 Water-based aerosols An aerosol vessel is filled with a mixture of 0.2 part of each of the present compounds (1) to (687), 0.2 part of d-allethrin, 0.2 part of d-phenothrin, 5 parts of xylene, 3,4 parts of deodorized kerosine, and 1 part of an emulsifier (ATMOS 300 available from Atlas Chemical Co.); and 50 parts of pure water. The vessel is equipped with a valve, through which 40 parts of a propellant (liquefied petroleum gas) are charged under increased pressure to give a water-based aerosol of each compound. Formulation Example 9 Mosquito-coils First, 0.3 g of each of the present compounds (1) to (687) is mixed with 0.3 g of d-allethrin, and the mixture is dissolved in 20 ml of acetone. The solution is uniformly mixed with 99.4 g of a carrier for mosquito-coils (prepared by mixing Tabu powder, pyrethrum marc powder and wood flour in the ratio of 4 : 3 : 3) under stirring. The mixture is well kneaded with 120 ml of water, molded, and dried to give a mosquito-coil of each compound. Formulation Example 10 Electric mosquito-mats First, 0.4 g of each of the present compounds (1) to (687), 0.3 parts of d-allethrin, and 0.4 g of pipenyl butoxide are dissolved in acetone to have a total volume of 10 ml. Then, 0.5 ml of the solution is uniformly absorbed in a substrate for electric mosquito-mats having a size of 2.5 cm x 1.5 cm and a thickness of 0.3 cm (prepared by forming a fibrillated mixture of cotton linter and pulp into a sheet) to give an electric mosquito-mat of each compound. Formulation Example 11 Heating smoke formulations First, 100 mg of each of the present compounds (1) to (687) is dissolved in a suitable amount of acetone. The solution is absorbed in a porous ceramic plate having a size of 4.0 cm x 4.0 cm and a thickness of 1.2 cm to give a heating smoke formulation of each compound. Formulation Example 12: Poison baits First, 10 mg of each of the present compounds (1) to (687) is dissolved in 0.5 ml of acetone, and the solution is uniformly mixed with 5 g of solid bait powder for animals (Breeding Solid Feed Powder CE-2 available from Japan Clea Co., Ltd.). The removal of acetone by air drying gives a 0.5% poison bait of each compound. The following test examples are provided for demonstrating that the present compounds are useful as active ingredients of insecticidal/acaricidal agents. In these test examples, the present compounds are designated by their compound numbers as describe above and the compounds used for comparison are designated by their compound symbols as described below. Compound (A): 4-(3-chloro-2-propenyloxy)phenoxyacetone 0-ethyl-oxime (i.e., compound 9 as described in JP-A 61-72733, page 7) Compound (B): 4-phenoxy-benzaldehyde 0-(3-methylbutyl)oxime (i.e., compound 41 as described in JP-A 61-260054, page 4) Test Example 1 Insecticidal test against Spodoptera litura A 200-fold water dilution (500 ppm) of a test compound formulation obtained according to Formulation Example 1 or 2 was absorbed at a volume of 2 ml in an artificial diet (Insecta LF available from Nihon Nosan K.K.) having a weight of 13 g, which had been prepared in a polyethylene cup having a diameter of 11 cm. Five fourth-instar larvae of Spodoptera litura were set free in the cup. After 6 days, the survival of the larvae was examined to determine the mortality. As a result, it was found that the present compounds (1)-(31), (33), (34), (47), (74).(76), (90), (91), (103), (104), (131), (133), (134), (147)-(150), (152)-(186), (203), (279)-(393), (481), (523)-(556), (558)-(572), (574)-(597), and (688)-(695) exhibited a mortality of 80% or higher. In contrast, compounds (A) and (B) exhibited the mortality of 0%. Test Example 2 Insecticidal test against Plutella xylostella To a water dilution (50 ppm) of a test compound formulation obtained according to Formulation Example 1 was added a spreading agent (New RINOU available from Nihon Noyaku K.K,) at a dilution ratio of 3000-fold. The dilution was sprayed over potted cabbages at the four to five leaf stage at a volume of 25 ml per pot. After the treated plants were air dried, ten third-instar larvae of Plutella xylostella were set free on each pot. After 4 days, the mortality was determined. As a result, it was found that the present compounds (l)-(22), (24)-(29), (33), (34), (47), (75), (76), (90), (91), (103), (104), (134), (153)-(161), (163)-(176), (180), (182)-(185), (279), (281), (283), (285), (287)-(299), (301)-(313), (315)-(321), (327), (332), (334), (336), (338)-(342), (351)-(360), (362)-(368), (370), (372)-(374), (376)-(382), (384)-(389), (391)-(393), (523), (524), (528)-(550), (558)-(566), (568)-(570), (573), (574), (576)-(579), (581)-(584), (589), (591)-(597), and (689)-(693) exhibited a mortality of 80% or higher. In contrast, compound (A) exhibited the mortality of 0%, Test Example 3 Insecticidal test against Heliothis virescens A water dilution (100 ppm) of a test compound formulation obtained according to Formulation Example 1 was added dropwise at a volume of 0.2 ml and uniformly spread over the surface of an artificial diet having a weight of 3 g, which had been prepared in a 30 ml plastic cup. After air drying, one second-instar larva of Heliothis virescens was set free in each cup. Ten larvae were used for each treatment. After 7 days, the mortality of the larvae was determined. As a result, it was found that the present compounds (3), (5), (11), (14)-(17), (25)-(27), (33), (34), (47), (76), (90), (91), (104), (134), (153)-(156), (160), (161), (163)-(169), (171)-(175), (281)-(300), (305)-(310), (312)-(331), (338)-(343), (346), (347), (350)-(359), (523), (528)-(531), (533)-(540), (542)-(551), (559), and (561)-(564) exhibited a mortality of 80% or higher. Test Example 4 Insecticidal test against Helicoverpa armigera A cotton leaf fragment (diameter, 5 cm) was immersed for 10 seconds in a water dilution (100 ppm) of a test compound formulation obtained according to Formulation Example 1. This fragment was taken out from the dilution, air dried, and placed in a polyethylene cup having a diameter of 5.5 cm. One third-instar larva of Helicoverpa armigera was set free in each cup. Ten larvae were used for each treatment. After 5 days, the mortality of the larvae was determined. As a result, it was found that the present compounds (2)-(6), (11), (14), (17), (24)-(26), (91), (104), (279), (283), (288), (291), (293), (303), (312), (318), (327), (329), (342), (355), (357), (358), (529), (531), (545), (562), (564), and (582) exhibited a mortality of 80% or more. In contrast, compound (A) exhibited the mortality of 0%. Test Example 5 Insecticidal test against Cydia pomonella A water dilution (100 ppm) of a test compound formulation obtained according to Formulation Example 1 was added dropwise at a volume of 0.2 ml and spread over the surface of an artificial diet having a weight of 3 g, which had been prepared in a 30 ml polyethylene cup. After air drying, placed in the cup was a piece of wax paper (about 2.5 cm square) having about 20 eggs which had been laid by Cydia pomonella and were just before hatching. Four pieces of such wax paper were used for each treatment. After 7 days, the mortality of the larvae was determined. As a result, it was found that the present compounds (l)-(3), (6), (10), (11), (14)-(16), (25), (27), (33), (34), (47), (76), (90), (91), (153)-(156), (158)-(176), (279), (289)-(291), (293), (294), (297), (300), (306), (307), (309)-(315), (317)-(319), (323), (324), (326)-(331), (338)-(340), (352)-(359), (365), (378), (379), (381), (382), (481), (528)-(531), (533)-(540), (542)-(546), (549), (550), (558)-(566), (568)-(570), (572), (574), (575), (578), and (579) exhibited a mortality of 80% or higher. Test Example 6 Acaricidal test against Tetranychus urticae About twenty female adults of Tetranychus urticae were set free on brush bean {Phaseolus vulgaris) in the primary leaf stage, which had been potted in a plastic cup for 7 days after the seeding. After 6 days, a 200-fold water dilution (500 ppm) of a test compound formulation obtained according to Formulation Example 1 or 2 was sprayed at a volume of 15 ml over the plant. After 8 days, each compound was evaluated for acaricidal activity on the following criteria. almost no damage and completely no surviving mites slight damage and some few surviving mites +: rather smaller damage and a rather fewer surviving mites than non-treatment case ++: same as non-treatment case As a result, it was found that the present compounds (6), (104), (173), (178), (306), (318), (327), (542), (582), (583), (589), (592), and (593) were evaluated at --- or -±-. In contrast, compounds (A) and (B) were evaluated at-+-. Test Example 7 Insecticidal test against Musca domestica In the bottom of a polyethylene cup having a diameter of 5.5 cm was placed a piece of filter paper having the same size. A 200-fold water dilution (500 ppm) of a test compound formulation obtained according to Formulation Example 1 was added dropwise at a volume of 0.7 ml on the filter paper, and about 30 mg of sucrose as a diet was uniformly placed thereon. Ten female adults of houseflies {Musca domestica) were set free in the cup, and the cup was kept covered. After 1 day, the survival of the adults was determined to determine the mortality. As a result, it was found that the present compounds (1), (4), (6), (7), (11)-(16), (18), (19), (22), (28), (29), (153), (155), (158), (159), (165)-(167), (170), (173), (175), (176), (180), (203), (287), (305), (307), (309), (318), (330), (332), (372)-(374), (376), (378), (481), (541), (542), (545), (551), (560), (565), (566), and (689) exhibited a mortality of 80% or higher. In contrast, compounds (A) and (B) used for comparison exhibited the mortality of 0%. Industrial Applicability The present compounds have excellent insecticidal/acaricidal activity, so that they are satisfactorily effective for the control of noxious insects, mites and ticks. 44. The oxime compound according to claim 5, 29, 30, 31, 32, 33, 34, 35, 36, 37, or 38, wherein A1 is A1-12. 45. The oxime compound according to claim 40, wherein G2 is oxygen. 46. The oxime compound according to claim 41, wherein Q1 is oxygen. 47. The oxime compound oxygen. 48. The oxime compound according to claim 5, 29, 30, 31, 32, 33, I 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, or 47, wherein G1 is G1-1. 49. The oxime compound according to claim 5, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, or 47, wherein G1 is G1-2. 50. The oxime compound according to claim 49, wherein Q2 is oxygen. ) 51. The oxime compound according to claim 5, 29, 30, 31, 32, 33, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50, wherein R^ is hydrogen, Ci-Cg alkyl, Cg-Cg haloalkyl, C-y^i al'co ;], C^-CG haloiillienyl. C3-C6 alkynyl, or C3-C6 haloalkynyl, or C3-C7 cycloalkyl optionally or C4-C10 cycloalkylalkyl optionally substituted the ring thereof, or C6-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, or C6-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof 52. The oxime compound according to claim 5, 29, 30, 31, 32, 33, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50, wherein R6 is T1-l or T1-2. 53. The oxime compound according to claim 5, 29, 30, 31, 32, 33, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49. or 50, wherein R^ is hydrogen. 54. The oxime compound according to claim 5, 29, 30, 31, 32, 33. 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, or 55. The oxime compound according to are independently halogen or C1-C3 alkyl; R4 is 3,3-dichloro-2-propenyl; a is 0; Y and Z are both oxygen; R6 is C1-C5 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl or C3-C6 haloalkenyl; AMsA'-7; G1 is G1-.l; al is 0; W is 1,3-phenylene or 1,4-phenylene, h and p are both 0; and R19, R20, R25, R26, R29, abd R30 ARE ALL hydrogen. 56. The oxime compound according to claim 5, wherein R2 and R3 are independently halogen or C1-C3 alkyl; R4 is 3,3-dichloro-2-propenyl; a is 0; Y and Z are both oxygen; R6 is C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl or C3-C6 haloalkenyl; A1 is A1-8 G1 is G1-1; al is 0; G2 is oxygen; or a heterocyclic 6-membered ring, exclusive of pyridine ring, containing at least one oxygen, sulfur, or nitrogen atom, which heterocyclic 6-membered ring may be optionally substituted with one to three identical or different (R16)g's wherein R18 and g are as defined in claim 1, or a heterocyclic 5-membered ring containing at least one oxygen, sulfur, or nitrogen atom, which heterocyclic 5-membered ring may be optionally substituted with one to three identical or different (R18)g'8 wherein R18 of which heterocyclic rings may be optionally substituted with one to three identical or different (R18)g s wherein R18 and g are as defined in claim 1, or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring. 59. The oxime compound according to claim 3, wherein R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C5 haloalkynyl, C2-C6 alkoxyalkyl, or C2-C10 alkylthioalkyl, 67. The oxime compound according to claim 3, 67, 58, 59, 61, 62, or 63, wherein A1 is A1--4. 68. The oxime compound according to claim 3, 67, 58, 69, 61, 62, or 63, wherein A2 is A2-5. 69. The oxime compound 59, 61, 62, or 63, wherein A2 is A2-6. 70. The oxime compound according to claim 3, 57, 58, 59, 61, 62, or 63, wherein A2 is A2-7 or A2-9. 71. The oxime compound according to claim 3, 57, 58, 59, 61, 62, are both 0; and R19, R20 R25 R26 R27, R25 R31, and R32 are all hydrogen. 83. The oxime compound wherein h and p are both 0; and R19 R20, R25 R26, R29, R30, R36 84. The oxime compound according to are both 0; and R19 R20, R25, R26 R29 R30, R35 and R36 are all hydrogen. 85. The oxime compound according to claim 79, wherein h and p are both 0; and R19 R20, R25, R26, R27, R28, R31, R32 R35, and R6 me all 95. The compound according to claim 1, which is 5-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal O-tert-butyloxime. 96. The compound according to claim 1, which is 6-(2,6-dichloro- 4-(3.3-dichloro-2-propenyloxy)phenoxy)hexanal 0-tert-butyloxime. 97. The compound according to claim 1, which is 4-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal 0-(2,2,2'-trichlovoethyl)- oxime. 98. The compound according to claim 1, which is 5-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal 0-(2,2,2-trichloroethyl)-oxime, 99. The compound according to claim 1, which is 6-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal 0-(2,2,2-trichloroethyl) oxime. 100. The compound according to claim 1, which is 4-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal 0 (3, 7 dichloro-2-propenyl)- oxime. 101. The compound according to claim 1, which is 5-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal 0-(3,3-dichloro-2-propenyl)- oxime. 102. The compound according to claim 1, which is 6-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal 0-(3,3-dichloro-2-propenyl)- oxime. 103. The compound according to claim 1, which is 1-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-isopropyl- oxime. 104. The compound according to claim 1, which is 5-(2,6-dichlo 4-(3,3-dichloro-2-propenyloxy)phenoxy) oxime. i 105. The compound according to claim 1, which is 4-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetone 0-isopropyloxime. 106. The compound according to claim 1, which is 5-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-isopropyloxime. 107. The compound according to claim 1, which is 4-(2,6-dichloro- 4-(3.3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-tert-butyl- oxime. 108. The compound according to claim 1, which is 5-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde 0-tert-butyl-oxime. 109. The compound according to claim 1, which is 4-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetone 0-tert-butyloxime. 110. The compound according to 4-(3,3-dichloro-2-propenyloxy)phenoxy) 111. The compound according to claim 1, which is 4-(2,6-dichloro- 4-(3.3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-(2,2,2-tri- chloroethyl)oxime. 112. The compound according to claim 1, which is 5-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde 0-(2,2,2-tri- chloroethyl)oxime. 113. The compound according to claim 1, which is 4-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetone 0-(2,2,2-trichloro- ethyl)oxime. 114. The compound according to claim 1, which is 5-(2.6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy) ethyl)oxime. 115. The compound according to claim 1, which is 4-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-(3,3-dichlo- ro-2-propenyl)oxime, 116. The compound according to claim 1, which is 5-(2,6-dichlon) 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde 0-(3,3-dichlo' ro-2-propenyl)oxime. 117. The compound according to claim 1, which is '4-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetone 0-(3,3-dichloro-2- propenyl)oxime. 118. The compound according to claim 1, which is 5-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime. 119. The compound according to claim 1, which is 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyib3nzaldehyde 0-sec-butyl-oxime. 120. The compound according to claim 1, which is 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methylbenzaldehyde 0-t-butyl-oxime. 121. The compound according to claim 1, which is 4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde 0-sec-butyl-oxime. 122. The compound according to claim 1, which is 4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde 0-alIyloxime. 123. The compound according to claim 1, which is 4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde 0-(3,3-dichIo-ro-2-propenyl)oxime, 124. The compound according to claim 1, which is 4-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzaldehyde 0-n-pro-pyloxime. 125. The compound according to claim 1, which is 4-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzaldehyde 0-isopro-pyloxime. 126. The compound according to claim 1, which is 4-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzdldehyde 0-sec- butyloxime. 127. The compound according to claim1, which is 4-(3-(2,β-clichlo ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)prbonzaldehyde 0-t-buty) oxime. 130. The compound according to claim 1, which is 4'-(4-(2,6-dichlo- ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)acetophenone 0-ethyl- oxime, 131. The compound according to claim 1, which is 4'-(4-(2,fl (lichlo ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)acetophenone O-n-plo pyloxime. 132. The compound according to claim 1, which is 4-(4-(2,6-dichulo- ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)benzaldehyde 0-isopro- pyloxime. 133. The compound according to claim 1, which is 4--(3-(2,6-di- chloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)-2,2,2-trifluoro- acetophenone 0-ethyloxime. 134. The compound according to claim 1, which is 4-(trifluoro- methyl)benzaldehyde 0-(4-(2,6-dichlcro-4-(3,3-dichloro-2-propenyloxy)phe- noxy)butyl)oxime. 135. The compound according to claim 1, which is 4'-(trifluoro- methyl)acetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe- noxy)butyl)oxime, 136. The compound according to claim 1, which is trimethyl- acetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichIoro-2-propenyloxy)phenoxy)pen- tyl)oxime. 137. The compound according to claim 1 which is 3,3-dimethyl-2- butanone O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)ph8noxy)pentyl)-oxime. 138. The compound according to claim 1, which is 3,3-dimethyl-2- butanoneO-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)- oxime. 139. The compound according to claim 1, which is 4-methyl-2- pentanone O-(4-(2,6-dichloro-4-(3.3-dichloro-2-propenyloxy)phenoxy)butyl)- oxime. 140. The compound according to claim 1, which is 4-methyl-2- pentanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)- oxime. 141 The compound according to claim 1, which is 3'methyl-2-butanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)-oxime. 142. An insecticidal/acaricidal agent comprising as an active ingredient, an oxime compound according to any one of claims 1 to 141. 143. A method for the extermination of insects, ticks or mitrw, comprising applying to the insects, ticks or mites, or to their habitats, an effective amount of an oxime compound according to any one of claims 1 to 141. R2 and R3 are both chlorine; R4 is 3,3-dichloro-2-propenyl; and R7 is hydrogen or methyl. 152. The compound according to claim 1, which is 4-(2,6-dlrhloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal oxime. 153. The compound according to claim 1, which is 5-(2,6-dichloro 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanai oxime. 154. The compound according to claim 1, which is 6-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal oxime. 155. The compound according to claim 1, which is 4-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde oxime. 156. The compound according to claim 1, which is 5-(2,6-dichloro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde oxime. 157. The compound according to claim 1, which is 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy ace tone oxime. 158. A hydroxylamine compound of formula (12) independently hydrogen, C1-C3 alkyl, or trifluoromethyl; h is an integer of 0 or 1; j is an integer of 1 to 3; m is an integer of 1 to 3; n is an integer of 1 to 3; p is an integer of 0 or 1; t is an integer of 0 to 3; u is an integer of 0 to 3; fl is an integer of 1 to 3; Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2; E is C5-C6 cycloalkylene; U3 is U3-1, U3-2, or U3-3 of formula (10) wherein: R35 and R36 are independently hydrogen, C1-C3 aikyi, or trifluoromethyl; (R40)g1's are zero to four identical or different substi-tuents selected from halogen, G1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy; R and V are independently -CH= or nitrogen; gl is an integer of 0 to 4; h1 is an integer of 1 to 3; i is an integer of 2 or 3; A2-8 or A2-10; or a salt thereof. 169. The hydroxylamine compound according to 161, wherein h and p are both 0; and R19 R20 R25 R26. R29 and R30 are all hydrogern or a salt thereof. 177. The amine compound according to claim 158, which is 0-(3- (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)hydroxylamine hydrochloride. 178. The amine compound according to claim 158, which is 0-(4- (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)hydroxylamine hydrochloride. 179. The amine compound according to claim 158, which is 0-(5- (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)hydroxyJamin«i hydrochloride. 180. The amine compound according to claim 158, which is 0-(β- (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)hydroxylamine hydrochloride. 181. A compound of formula (13) I / haloalkyl, C1-C3 alkoxy, or C1-C8 haloalkoxy; and R19 and R20 are both hydrogen. 183. The compound according to claim 187, which is3,5-ditihloro- l-(3,3-dichloro-2-propenyloxy)-4-(4-formylbenzyloxy)benzenoi 184. The compound according to claim 181, which is 3,5-dichlom- l-(3,3-dichloro-2-propenyloxy)-4-(4-acetylbenzyloxy)benzene. : 185. The compound according to claim 185, which is 3,5-dichloro- l-(3,3-dichloro-2-propenyloxy)-4-(4-formylphenethyloxy)benzene. 186. The compound according to claim 185, which is 3,5-dichloro- l-(3,3-dichloro-2-propenyloxy)-4-(4-acetylphenethyloxy)benzene. 187. The compound according to claim 185, which is 3,5-dichloro- l-(3,3-dichloro-2-propenyloxy)-4-(5-formyl-2-furylmethoxy)benzene. 188. A compound of formula (14) R19 R20, R29 and R30 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl; j is an integer of 1 to 3; and V is an integer of 1 to 4. 189. The compound according to claim 188, wherein R2 and R3 are independently halogen or C1-C3 alkyl; R7 is hydrogen, C1-C8 alkyl, or C1-C3 haloalkyl, or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy; and R19 R2o R29 and R30 are all hydrogen. 190. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(3-(4-formylphenoxy)propoxy)benzene. 191. The compound according to claim 188, which is 3,5-dichloro-1.-(3,3-dichloro-2-propenyloxy)-4-(4-(4-formylphenoxy)butoxy)benzene. 192. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-formylphenoxy)pentyloxy)benzene. 193. The compound according to claim 188, which is 3,5-dichloro-l'(3,3-dichloro-2-propenyloxy)-4-(3-(4-acetylphenoxy)propoxy)benzene. 194. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(4-(4-acetylphenoxy)batoxy)benzene. 195. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-acetylphenoxy)pentyioxy)bonzene. 196. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(3-(4-(trifluoroacetyl)phenoxy)propoxy)-benzene. 197. The compound according to claim 188, which is 3,5-dichloro- ■J ■ l-(3,3-dichloro-2-propenyloxy)-4-(4-(4-(trifluoroacetyl)phenoxy)butoxy)- benzene. 198. The compound according to claim 188, which is 3.5-dichloro- l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-(trifluoroacetyl)phenoxy)pentyloxy)- benzene. 199. The compound according to claim IBS. whhichis 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(3-(4-propionylphenoxy)propoxy)benzene. 200. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(4-(4-propionylphenoxy)butoxy)benzene, 201. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-propionylphenoxy)pentyloxy)benzene. 202. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(3-(4-benzoylphenoxy)propoxy)benzene. 203. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(4-(4-benzoylphenoxy)butoxy)benzene. 204. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-benzoylphenoxy)petyloxy)benzene. 205. The compound according to claim i, winch is 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methylbenzaldehyde oxime. 206. The compound according to claim 1, which is 4'-((2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyl)acetophenone oxime. 207. The compound according to claim 1, which is 4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde oxime. 208. The compound according to claim 1, which is .4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)acetophenone oxime, 209. The compound according to claim 1, which is 4-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzaldehyde oxime. 210. The compound according to claim 1, which is 4-(4-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)bexbleyde oxime. 211. The compound according to claim 1, which is 4-(5-(2,6-dichlo- ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)bonzaldehyde oxime. 212. The compound according to claina, (3-(2,6-dichlo-ro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)acelophenone oxime. 213. The compound according to claim 1, which is 4'-(4-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)acetophenone oxime. 214. The compound according to claim 1, which is 4'-(5-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)acetophenone oxime. 215. The compound according to claim 1. which is 4'-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)-2,2,24rifluoroacetophe-none oxime. 216. The compound according to claim 1, which is 4'-(4-(2,β illchlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)-2,2,2-trifluoroacetophe none oxime. 217. The compound according to claim 1, which is 4-(5-(2,6-diehlo- ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)-2,2,2-trifluoroacetophe-none oxime. 218. The compound according to claim 1, which is 4'"(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)propiophenone oxime. 219. The compound according to claim 1, which is 4'-(4-(2,6-dichlo- ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)propiophenone oxime. 220. The compound according to claim 1, which is 4'-(5-(2,6-dichlo- ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)propiophenone oxime. 221. The compound according to claim 1, which is 4'-(3-(2,6-dichlo- ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyioxy)ben2ophenone oxime. 222. The compound according to claim 1, which 4-(4-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)ben2ophenone oxime. 223. The compound according to claim 1, which is 4-(5-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)benzophenone oxime. 224. A phenol compound of formula (50) wherein: R1 R2, and R3 are independently halogen, C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1-C3 haloalkoxy, nitro, or cyano; a is an integer of 0 to 2; Z is oxygen, sulfur, or NR5 wherein R5 is hydrogen, acetyl, or C1-C3 D is -CH= or nitrogen; J is oxygen or sulfur; b is an integer of 0 to 5; d is an integer of 1 to 3; e is an integer of 0 to 3; f is an integer of 2 to 4; alkyl, C1-C3 haloalkyl, C1-C4 alkoxy, or C1-C3 haloalkoxy; and R'16 and R42 are independently C1-C6 alkyl, C2-C6 wherein: (R17)b's are zero to five identical or different substi-tuents selected from halogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C1-C6 alkoxy, C1-C3 haloalkoxy, C2-C6 alkenyloxy, C2-C6 haloalkenyloxy, C2-C6 alkynyloxy, C3-C6 haloalkynyloxy, C1-C3 alkylthio, C1-C3 haloalkylthio, C1-C2 alkylsulfinyl, C1-C2 alkylsulfonyl, C1-C2 haloalkylsulfinyl, CpCa haloalkylsulfonyl, together at their ends to form trimethylene or tetramethyl-ene, or when b is 2 to 5, two adjacent R17's are combined together at their ends to form methylenedioxy optionally substituted with halogen or C1-C3 alkyl, or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring; methyl; R22 is hydrogen, C1-C3 alkyl, or trifluoromethyl, or when h is 0 and i is 1 in A1-l, R22 and R7 may be combined together at their ends to form trimethylene, tetra-methylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl, or when h is 0 and j is 1, in A1-2, A1-3, A1-4, A1-5, or A1-6, R22 and R2 may be combined together at their ends to form trimethylene, tetramethylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl; h is an integer of 0 or 1; i is an integer of 1 to 6; j is an integer of 1 to 3; k is an integer of 2 to 8; m is an integer of 1 to 3; n is an integer of 1 to 3; p is an integer of 0 or 1; q is an integer of 0 or 1; r is an integer of 2 to 4; s is an integer of 2 to 4; t is an integer of 0 to 3; u is an integer of 0 to 3; V is an integer of 1 to 4; w is an integer of 1 to 4; X is an integer of 1 to 4; Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2; Q2 is oxygen, S(0)z, or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2; E is C5-C6 cycloalkylene; U1 is U1 of formula (6) wherein: W is an optionally substituted benzene ring or an optionally substituted heterocyclic ring; G1 is G1-l or G1-2 of formula (7) Q2 is oxygen, S(0)z,, or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2; R35 R36 R37 and R38 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl; al is an integer of 0 to 4; bl is an integer of 1 to 3; and dl is an integer of 0 to 2; and are independently hydrogen, C1-C8 alkyl, or trifluoromethyl; h is an integer of 0 or 1; j is an integer of 1 to 3; m is an integer of 1 to 3; n is an integer of 1 to 3; p is an integer of 0 or 1; t is an integer of 0 to 3; u is an integer of 0 to 3; f1 is an integer of 1 to 3; Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2; E is C6-C6 cycloalkylene; U1 is U3.l, U3-2, or U3-3 of formula (10) h1 is an integer of 1 to 3; i1 is an integer of 2 or 3; and Q2 is oxygen, S(0)„ or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2; U4 is U4-l, U4-2, or U'-3 of formula (11) wherein: R35 and R36 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl; (R40)g1's are zero to four identical or different substituents selected from halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy; R and V are independently -CH= or nitrogen; gl is an integer of 0 to 4; hi is an integer of 1 to 3; il is an integer of 2 or 3; Q2 is oxygen, S(0),, or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2; and Q3 is oxygen, S(0)e,i, or NR39 wherein R39 is hydrogen or C1-C3 alkyl, and el is an integer of 0 to 2. 225. The phenol compound according to claim 224, wherein Z is a is 0. 227. The phenol compound according to claim 224, 225, or 226, wherein R1 R2 and R3 are independently halogen or C1-C3 alkyl. 228. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 229. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X2 230. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-l, 231. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-2. 232. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-3. 233. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-4. 234. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-5. 1. 235: The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 arid A1 is A1-6. 236. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-7. 237. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-8. 238. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-9. 239. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-1O. 240. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X^ and A' is A'-ll. 241. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X' and A' is A'-12. 242. The phenol compound according to claim 224, wherein: X is X1 A1 isA1-1; R21 and R22 are both hydrogen; h is 0; i is an integer of 3 to 5; Z is oxygen; R2 and R3 are independently chlorine or C1-C3 alkyl; a is 0; R6 is C1-C5 alkyl, C2-C4 haloalkyl, C3-C6 alkenyl, or C3-C6 haloalkenyl; and R7 is hydrogen, C1-C4 alkyl, or trifluoromethyl; or wherein: X is X'; A1 is A1-2; R21, R22 R23 and R24 are all hydrogen; h is O; Q1 is oxygen; j is 1; k is an integer of 3 to 6; Z is oxygen; R2 and R3 are independently chlorine or C1-C3 alkyl; a is 0; R6 is C1-C5 alkyl, C2-C4 haloalkyl, C3-C6 alkenyl, or C3-C6 haloalkenyl; a is 0; Z is oxygen; X is X1 R6 is C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, or C3-C6 haloalkenyl; A1 is A1-7; I G1 is G1-1; al is 0; W is 1,3-phenylene or 1,4-phenylene; h and p are both 0; and ^19 1^20^ j^26 j^26^ j^29^ ^^^ R3O ^^^ ^^ hydrogen. 248. The phenol compound according to claim 224, wherein R^ and R^ are independently halogen or C2-C6 alkyl; a is 0; Z is oxygen; X is X1 R6 is C1-C8 alkyl, C2-C8 haloalkyl, C2-C8 alkenyl, or C3-C6 haloalkenyl; A1 isA1-8; G1 is G1-l; al is 0; G2 is oxygen; W is 1,3-phenylene or 1,4-phenylene; h and p are both 0; and R19, R2o, R25, R26, R29, and R3O ARE ALL hydrogen. 249. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X2 R8 and R9 are independently hydrogen, C1-C11, alkyl, C1-C6 haloalkyl, C2-C8 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C8 haloalkynyl, C2-C10 alkoxyalkyl, C2-C10 alkylthioalkyl, or naphthyl, or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or C2-C8 cycloalkenyl optionally substituted with C1-C4 alkyl, or C2-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, or T2-l or T2-2 of formula (4) I wherein R17, D, R11, R12 b, and d are as defined in claim 224, or 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, or 3-pyrrolyl, each of which heterocyclic rings may be optionally substituted with one to three identical or different (R18)g's wherein R18 and g are as defined in claim 223, or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring. 250. The phenol compound according to claim 224, 225, 226, or oxygen or sulfur atoms in the ring. 251. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A2-l. 252. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A2-2. 253. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A2-3. 254. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A2-A. 255. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A2-5. 256. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A'-6. 257. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A='-7 or A'-9. 258. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A2-8 or A2-10. 259. The phenol compound according to claim 251, wherein h and p are both 0; and R19 R20, R25 R26 R29 and R30 are all hydrogen. 260. The phenol compound according to claim 252, wherein h and p are both 0; R19 R20, R25 R26 R27, R28, R313, and R32' are all hydrogen; and Q1 is oxygen. 261. The phenol compound according to claim 253, wherein h and p are both 0; R19 R20, R25 R26 R29 R30, R35 and R36 are all hydrogen; and Q2 is oxygen. 262. The phenol compound according to claim 254, wherein h and p are both 0; R19 R20, R25 R26 R29 R30, R35 and R36 are all hydrogen; and Q1 and Q3 are both oxygen. 263. The phenol compound according to claim 255, wherein h and p are both 0; R19 R20 R25 R26 R27 R28 R31, R32 R35 and R36 are all hydrogen; and Q1 and Q2 are both oxygen. 264. The phenol compound according to claim 256, wherein h and p are both 0; R19 R20 R25 R26 R27 R28 R31, R32 R35 and R36 are all hydrogen; and Q1 Q2, and Q3 are all oxygen. 265. The phenol compound according to claim 257, wherein R19 R20 R23, R24, R25, R26, R29, R3o, R35 and R36 ARE ALL hydrogen; and Q1 and Q1 are both oxygen. 266. The phenol compound according to claim 258, wherein R19 R20 R23 R24 R25 R26 R35 and R36 are all hydrogen; and Q1 and Q2 are both oxygen. I ■ ' 267. The compound according to claim 224, which is 4-(2,6-dichlo- ro-4-hydroxyphenoxy)butanal 0-isopropyloxime. 268. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentanal 0-isopropyloxime. 269. The compound according to claim 224, which is 6-(2,6-dichlo-ro-4-hydroxyphenoxy)hexanal 0-isopropyloxime. 270. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butanal 0-tert-butyloxime. 271. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentanal 0-tert-butyloxime. 272. The compound according to claim 224, which is 6-(2,6-dichlo-ro-4-hydroxyphenoxy)hexanal 0-tert-butyloxime. 273. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butanal 0-(2,2,2-trichloroethyl)oxime. 274. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentanal 0-(2,2,2-trichloroethyl)oxime. 275. The compound according to claim 224, which is 6-(2,6-dichlo-ro-4-hydroxyphenoxy)hexanal 0-(2,2,2-trichloroethyl)oxime. 276. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butanal 0-(3,3-dichloro-2-propenyl)oxime. 277. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentanal 0-(3,3-dichloro-2-propenyl)oxime. 278. The compound according to claim 224, which is 6-(2,6-dichlo-ro-4-hydroxyphenoxy)hexanal 0-(3,3-dichloro-2-propenyl)oxime. 279. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-isopropyloxime. 280. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-isopropyloxime. 281. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetone 0-isopropyloxime. 282. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetone 0-isopropyloxime. 283. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-tert-butyloxime. 284. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-tert-butyloxime. 285. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxy\|)henoxy)butyloxyacetone 0-tert-butyloxime. 286. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetone 0-tert-butyloxime. 287. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime. 288. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime. 289. The compound according to claim 224, which is 4-(2,6-dichlo ro-4-hydroxyphenoxy)butyloxyacetone 0-(2,2,2-trichloroethyl)oxime. 290. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetone 0-(2,2,2-trichloroethyl)oxime. 291. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)-oxime. 292. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)-oxime. 293. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime. 294. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime. 295. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)methylbenzaldehyde 0-sec-butyloxime. 296. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)methylbenzaldehyde 0-t-butyloxime. 297. The compound according to claim 224, which is 4-(2-(2,6-di-chloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-sec-butyloxime. 298. The compound according to claim 224, which is 4-(2-(2,6-di-chloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-allyloxime. 299. The compound according to claim 224, which is 4-(2-(2,6-di-chloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)-oxime. r I I 300. The compound according to claim 224, which is 4-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-n-propyloxime. 301. The compound according to claim 224, which is 4-(3-(2,6-di- chloro-4-hydroxyphenoxy)propyloxy)benzaldehydeO-isopropyloxime. 302. The compound according to claim 224, which is 4-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)benzaldehydeO-sec-butyloxime. 303. The compound according to claim 224, which is 4-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-t-butyloxime. 304. The compound according to claim 224, which is 4'-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)acetophenone 0-ethyloxime. 305. The compound according to claim 224, which is 4'-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)propiophenone 0-ethyloxime. 306. The compound according to claim 224, which is 4'-(4-(2,6-di-chloro-4-hydroxyphenoxy)butyloxy)acetophenone 0-ethyloxime. 307. The compound according to claim 224, which is 4'-(4-(2,6-di-chloro-4-hydroxyphenoxy)butyloxy)acetophenone 0-n-propyloxime. 308. The compound according to claim 224, which is 4-(4'(2,6-di-chloro-4-hydroxyphenoxy)butyloxy)benzaldehyde 0-isopropyloxime. 309. The compound according to claim 224, which is 4'-(3-(2,6-di- chloro-4-hydroxyphenoxy)propyloxy)-2,2,2-trifluoroacetophenone 0-ethyloxime. 310. The compound according to claim 224, which is 4-(trifluoro-methyl)benzaldehyde 0-(4-(2,6-dichloro-4-hydroxyphenoxy)butyl)oxime. 311. The compound according to claim 224, which is 4'-(trifluoro-methyl)acetophenone 0-(4-(2,6-dichloro-4-hydroxyphenoxy)butyl)oxime. 312. The compound according to claim 224, which is trimethyl-acetaldehyde 0-(5-(2,6-dichloro-4-hydroxyphenoxy)pentyl)oxime. 313. The compound according to claim 224, which is 3,3-dimethyl-2-butanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)pentyl)oxime. 314. The compound according to claim 224, which is 3,3-dimethyl-2-butanone 0-(4-(2,6-dichloro-4-hydroxyphenoxy)butyl)oxime. , ' ■ ■ 1 , I 315. The compound according to claim 224, which is 4-methyI-2- pentanone 0-(4-(2,6-dichloro-4-hydroxyphenoxy)butyl)oxime. 316. The compound according to claim 224, which is 4-methyl-2- pentanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)pentyl)oxime. 317. The compound according to claim 224, which is 3-methyl-2- 4 butanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)pentyl)oxime. 318. A compound of formula (51) wherein: R57is C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, C3-C6 haloalkenyl, C3-C6 alkynyl, C3-C6 haloalkynyl, or triphenylmethyl, or C3-C7 cycloalkyl, optionally substituted C1-C4 alkyl, or C4-C10 cycloalkylalkyl, optionally substituted C1-C4 alkyl on the ring thereof, or C3-C6 cycloalkenyl, optionally substituted C1-C4 alkyl, or C3-C6 cycloalkenylalkyl, optionally substituted C1-C4 alkyl on the ring thereof, tuents selected from halogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 halo-alkynyl, C1-C6 alkoxy, C1-C3 haloalkoxy, C2-C6 alkenyloxy, C2-C6 haloalkenyloxy, C2-C6 alkynyloxy, C2-C6 haloalkynyloxy, (C1-C5 alkoxy)carbonyl, cyano, or nitro; R11, R12, R13, and R14 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl; D is -CH= or nitrogen; b is an integer of 0 to 5; d is an integer of 1 to 3; e is an integer of 0 to 3; f is an integer of 2 to 4; R7 is hydrogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 cycloalkyl, cyano, cyano C1-C3 alkyl, (C1-C4 alkoxy)carbonyl, or (C1-C4 alkoxy)carbonyl(C1-C3)alkyl, or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy, or benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof; R58 is hydrogen or C1-C4 alkyl; R59 is hydrogen or C1-C4 alkyl; or R59 and R7 may be combined together at their ends to form trimethylene, tetramethylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl; L7 is hydroxy, chlorine, bromine, iodine, mesyloxy, or tosyloxy; and G4 is G4.2, G4-3, or G4-4 of formula (53) G4-2: -(CR60R61)k- G4-4:-(CR60R61)M-C = C-(CR62R63)N-wherein: R60, R61 R62 R63 R64, and R65 ARE independently hydrogen or C1-C3 alkyl; k is an integer of 2 or 8; m is an integer of 1 to 3; and n is an integer of 1 to 3. 319. An oxime compound, substantially as herein described, and exempli f ied. 3 20. A phenol compound, substantially as herein described, and exemplified.

Full Text

DESCRIPTION
OXIME COMPOUNDS, THEIR USE, AND
INTERMEDIATES FOR THEIR PRODUCTION
Technical Field
The present invention relates to oxime compounds, their use, and intermediates for their production.
Background Art
As disclosed, for example, in JP-A 61-72733 and JP-A 61-260054, it is well known that certain types of oxime compounds can be used as the active ingredients of insecticides. These compounds are, however, not necessarily satisfactory for the active ingredients of insecticidal/acaricidal agents in view of their insecticidal activity.
Disclosure of Invention
Under these circumstances, the present inventors have extensively studied to find out compounds with excellent insecticidal/acaricidal activity. As a result, they have found that oxime compounds of formula (1) as depicted below have excellent insecticidal/acaricidal activity, thereby completing the present invention.
Thus, the present invention provides oxime compounds of formula (1)

(hereinafter referred to as the present compound(s)) wherein:

R1 R2 and R3 are independently halogen, C1-C3 alkyl, C1-C3 naioaiKyi, C1-C3 alkoxy, C1-C3 haloalkoxy, nitro, or cyano;
R4 is 3,3-dihalogeno-2-propenyl;
a is an integer of 0 to 2;
Y is oxygen, sulfur, or NH;
Z is oxygen, sulfur, or NR5 wherein R5 is hydrogen, acetyl, or Cj-Cg alkyl;
X is X1 or X2 of formula (2)

wherein:
R6 is hydrogen, C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, Cg-Cg haloalkenyl, C3-C6 alkynyl, C3-C6 haloalkynyl, or triphenyl-methyl,
or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl,
or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof,
or C5-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or Cfi-Cg cycloalkenylalkyl optionally substituted with Ci-C4 alkyl on the ring thereof,
or Ci-Cg alkyl substituted with cyano, nitro, (C1-C4 alkoxy)-carbonyl, C1-C4 alkylthio, or C1-C4 alkoxy,
or T1-l, T1-2, T1-3, T1-4, T1-5, T1-6, or T1-7 of formula (3)

(R10')b's are zero to five identical or different substi-tuents selected from halogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 halo-alkynyl, C1-C6 alkoxy, C1-C3 haloalkoxy, C3-C6 alkenyloxy, C2-C6 haloalkenyloxy, C2-C6 alkynyloxy, C3-C6 haloalkynyloxy, (C1-C5 alkoxy)carbonyl, cyano, or nitro;
R11, R12, R13, and R14 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
D is -CH= or nitrogen;
J is oxygen or sulfur;
b is an integer of 0 to 5;
d is an integer of 1 to 3;
e is an integer of 0 to 3;
f is an integer of 2 to 4;
R15 is C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, or C2-C6 cycloalkyl,
or phenyl optionally substituted with halogen, C1-C4

alkyl, C1-C3 haloalkyl, C1-C4 alkoxy, or C1-C3 haloalkoxy; and R16 and R42 are independently C1-C3 alkyl, C2-C6
haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl,
C3-C6 haloalkynyl, or C2-C6 cycloalkyl,
or phenyl optionally substituted with halogen, C1-C4
alkyl, C1-C3 haloalkyl, C1-C4 alkoxy, or C1-C3 haloalkoxy,
or benzyl optionally substituted with halogen, C1-C4
alkyl, C1-C3 haloalkyl, C1-C4 alkoxy, or C1-C3 haloalkoxy on
the ring thereof;
R7 is hydrogen, C1-C3 alkyl, C1-C3 haloalkyl, C2-C6 cycloalkyl, cyano, cyano C1-C3 alkyl, (C1-C4 alkoxy)carbonyl, or (C1-C4 alkoxy)-carbonyl(Ci-C3)alkyl,
or phenyl optionally substituted with halogen, Ci-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy,
or benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof;
R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C2-C10 alkoxyalkyl, C2-C10 alkylthioalkyl, or naphthyl,
or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl,
or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof,
or C2-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 on the ring thereof,
or T2-l or T2-2 of formula (4)

wherein:
(R17)b's are zero to five identical or different substi-tuents selected from halogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C1-C3 alkoxy, C1-C3 haloalkoxy, C2-C6 alkenyloxy, C2-C6 haloalkenyloxy, C2-C6 alkynyloxy, C2-C6 haloalkynyloxy, C1-C3 alkylthio, C1-C3 haloalkylthio, C1-C3 alkylsulfinyl, C1-C2 alkylsvdfonyl, C1-C3 haloalkylsulfinyl, C1-C2 haloalkylsulfonyl, C1-C3 hydroxyalkyl, C2-C4 alkoxyalkyl, C2-C4 alkylthioalkyl, dimethylamino, acetamido, acetyl, formyl, carboxyl, (C1-C3 alkyl)aminocarbonyl, [di(C1-C2 alkyl)amino]carbonyl, (C1-C3 alkoxy)carbonyl, C3-C6 cycloalkyl, C2-C6 cycloalkenyl, C2-C6 cycloalkyloxy, C2-C6 cycloalkenyloxy, pentafluorosulfanyl (FgS), cyano, or nitro,
or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy,
or phenoxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy,
or benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof,
or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof,
or when b is 2 to 5, two adjacent R17's are combined

together at their ends to form trimethylene or tetramethyl-
ene,
or when b is 2 to 5, two adjacent R^^'s are combined together at their ends to form methylenedioxy optionally substituted with halogen or C1-C3 alkyl,
or when b is 2 to 5, two adjacent R17's are combined together at their ends to form ethylenedioxy optionally substituted with halogen or C1-C3 alkyl;
D is -CH= or nitrogen;
R11 and R12 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
b is an integer of 0 to 5; and
d is an integer of 1 to 3; or a heterocyclic group, exclusive of pyridine ring, which heterocyclic group may be optionally substituted with one to three identical or different (R18)g s, wherein:
R18 is halogen, C1-C3 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C1-C3 alkoxy, C1-C3 haloalkoxy, C2-C6 alkenyloxy, C3-C6 haloalkenyloxy, C2-C6 alkynyloxy, C3-C6 haloalkynyloxy, C1-C3 alkylthio, C1-C3 haloalkylthio, C1-C2 alkylsulfinyl, C1-C3 alkylsulfonyl, C1-C2 haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3 hydroxyalkyl, C2-C4 alkoxyalkyl, C2-C4 alkylthioalkyl, cyano, or nitro,
or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy; and
g is an integer of 1 to 3;

or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring;
A1 is A1-l, A1-2. A1-3, A1-4, A1-5, A1-6, A1-7, A1-8, A1-9, A1-10,

methyl;
R22 is hydrogen, C1-C3 alkyl, or trifluoromethyl,
or when h is 0 and i is 1 in A^-1, R^^ and R^ may be combined together at their ends to form trimethylene, tetra-methylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl,
or when h is 0 and j is 1, in A1-2, A1-3, A1-4, A1-5, or A1-6, R22 and R7 may be combined together at their ends to form trimethylene, tetramethylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl;
h is an integer of 0 or 1;
i is an integer of 1 to 6;
j is an integer of 1 to 3;
k is an integer of 2 to 8;
m is an integer of 1 to 3;
n is an integer of 1 to 3;
p is an integer of 0 or 1;
q is an integer of 0 or 1;
r is an integer of 2 to 4;
s is an integer of 2 to 4;
t is an integer of 0 to 3;
u is an integer of 0 to 3;
V is an integer of 1 to 4;
w is an integer of 1 to 4;
X is an integer of 1 to 4;
Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2;
Q2 is oxygen, S(0)z, or NR34 wherein R34 is hydrogen

or C1-C3 alkyl, and z is an integer of 0 to 2; E is C5-C6 cycloalkylene; U1 is U1 of formula (6)
-G1-W-wherein:
W is an optionally substituted benzene ring or an optionally substituted heterocyclic ring;
G1 is G1-l or G1-2 of formula (7)

Q2 is oxygen, S(0)z, or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2;
R35 R36 R37 and R38 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
al is an integer of 0 to 4;
bl is an integer of 1 to 3; and
dl is an integer of 0 to 2; and G2 is oxygen, 8(0)a1, or NR39 wherein R39 is

h is an integer of 0 or 1; j is an integer of 1 to 3; m is an integer of 1 to 3; n is an integer of 1 to 3; p is an integer of 0 or 1; t is an integer of 0 to 3; u is an integer of 0 to 3; fl is an integer of 1 to 3;
Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2; E is C2-C6 cycloalkylene; U3 is U3-l, U3.2, or U3-3 of formula (10)

wherein:
R35 and R36 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
(R40)gi's are zero to four identical or different substituents selected from halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy;
R and V are independently -CH= or nitrogen;
gl is an integer of 0 to 4;

wherein:
R35 and R36 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
(R40)gi's are zero to four identical or different substituents selected from halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy;
R and V are independently -CH= or nitrogen;
gl is an integer of 0 to 4;
hi is an integer of 1 to 3;
il is an integer of 2 or 3;
Q2 is oxygen, S(0)„ or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2; and
Q3 is oxygen, 8(0)e,1, or NR39 wherein R39 is hydrogen or C1-C3 alkyl, and el is an integer of 0 to 2; and insecticidal/acaricidal agents containing them as active ingredients.
In particular, the oxime compounds of formula (1) wherein X is X1 and R6 is hydrogen are useful both as the active ingredients of insecticidal/-

acaricidal agents and as the intermediates for the production of these active ingredient compounds.
The present invention further provides hydroxylamine compounds of formula (12)

wherein R1 R2, R3, R4 a, Y, Z, and A2 are as defined above, and salts thereof (e.g., inorganic acid salts such as hydrochlorides, sulfates, and nitrates). The present invention further provides compounds of formula (13)

wherein R2 R3 R7 R19, R20, and j are as defined above, and R41 is 3,3-di-chloro-2-propenyl, 3,3-dibromo-2-propenyl, or 3-bromo-3-chloro-2-propenyl, which are useful as the intermediates for the production of the present compounds.
The present invention further provides compounds of formula (14)

wherein R2, R3 R7 R19 R20 R29 R30 R41 j, and v are as defined above, which are useful as the intermediates for the production of the present compounds.

The present invention further provides phenol compounds of formula (50)

wherein R1 R2, R3, a, X, and Z are as defined above, with the proviso that when X is X1 R6 is not hydrogen, which are useful as the intermediates for the production of the present compounds.

ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, 1-ethylpropyl, n-hexyl, isohexyl, 2-ethyl-butyl, 1-methylpentyl, 1-ethylbutyl, 3-methylpentyl, 1,3-dimethylbutyl, n-heptyl, 1-ethyl-l-methylbutyl, n-octyl, and 1-methylheptyl.
The C1-C6 alkyl represented by R7 R10 R15 R16 R42 R17 or R18 may include, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, 1-ethylpropyl, n-hexyl, isohexyl, 2-ethylbutyl, 1-methylpentyl, 1-ethylbutyl, 3-methylpentyl, and 1,3-dimethylbutyl.
The C1-C11 alkyl represented by R8 or R9 may include, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl,

n-pentyl, isopentyl, neopentyl, tert-pentyl, 1-ethylpropyl, n-hexyl, isohexyl, 2-ethylbutyl, 1-methylpentyl, 1-ethylbutyl, 3-methylpentyl, 1,3-dimethyl-butyl, n-heptyl, l-ethyl-l-methylbutyl, n-octyl, 1-methylheptyl, n-nonyl, n-decyl, and n-undecyl.
The C1-C4 alkyl represented by R40 may include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, and tert-butyl.
The C1-C3 haloalkyl represented by R1 R2, R3 R7 R10 R15 R17 R18, or R40 may include, for example, trifluoromethyl, difluoromethyl, bromo-difluoromethyl, 1-fluoroethyl, 1-chloroethyl, 1-bromoethyl, perfluoroethyl, 2-bromo-l,l,2,2-tetrafluoroethyl, 1,1,2,2-tetrafluoroethyl, 2-chloro-l,l,2-tri-fluoroethyl, 2-bromo-l,l,2-trifluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloro-ethyl, 2,2,2-tribromoethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodo-ethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3, 3-hexafluoropropyl, l,l,l,3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloro-propyl, 2-bromopropyl, 2-iodopropyl, and 2,3-dibromopropyl
The C2-C6 haloalkyl represented by R6, R16, or R41 may include, for example, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoropropyl, 1,1,1, 3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bromopropyl, 2-iodopropyl, 2,3-dibromopropyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl, 4-iodobutyl, 3-chloro-2,2-dimethylpropyl, 3-bromo-2,2-dimethylpropyl, 2,2,3, 3,4,4,5,5-octafluoropentyl, 6-chlorohexyl, and 6-bromohexyl
The C1-C6 haloalkyl represented by R8 or R9 may include, for example, trifluoromethyl, trichloromethyl, difluoromethyl, bromodifluoromethyl, 2,2, 2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, 2-fluoroethyl,

2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopro-pyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoropropyl, 1,1,1,3,3,3-hexa-fluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bromopropyl, 2-iodopropyl, 2,3-dibromopropyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl, 4-iodobutyl, 3-chloro-2,2-dimethylpropyl, 3-bromo-2,2-dimethylpropyl, 2,2,3,3,4,4,5,5-octafluoropentyl, 6-chlorohexyl, and 6-bromohexyl
The C1-C3 alkoxy represented by R1 R2, R3, or R40 may include methoxy, ethoxy, n-propyloxy, and isopropyloxy.
The C1-C3 alkoxy represented by R10, R17 and R18 may include, for example, methoxy, ethoxy, n-propyloxy, isopropyloxy, n-butyloxy, isobutyloxy, sec-butyloxy, tert-butyloxy, n-pentyloxy, isopentyloxy, neopentyloxy, tert-pentyloxy, 1-ethylpropyloxy, n-hexyloxy, isohexyloxy, 2-ethylbutyloxy, 1-methylpentyloxy, 1-ethylbutyloxy, 3-methylpentyloxy, and 1,3-diemthyl-butyloxy.
The C1-C3 haloalkoxy represented by R1 R2 R3 R10 R17 R18, or R40 may include, for example, trifluoromethoxy, bromodifluoromethoxy, 1-fluoro-ethoxy, 1-chloroethoxy, 1-bromoethoxy, perfluoroethoxy, 2-bromo-l,l,2,2-tetrafluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-chloro-1,1,2-trifluoroethoxy, 2-bromo-l,l,2-trifluoroethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy-ethoxy, 2,2,2-tribromoethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2-dichloroethoxy, 2,2-dibromoethoxy, 3-fluoropropyloxy, 3-chloropropyloxy, 3-bromopropyloxy, 3-iodopropyloxy, 3,3,3-trifluoropropyloxy, 2,2,2,3,3,3-hexafluoropropyloxy, 1,1,1,3,3,3-hexa-fluoro-2-propyloxy, 2-fluoropropyloxy, 2-chloropropyloxy, 2-bromopropyloxy, 2-iodopropyloxy, and 2,3-dibromopropyloxy.
The C3-C6 alkenyl represented by R6, R16, or R42 may include, for example, allyl, 2-butenyl, 3-butenyl, l-methyl-2-propenyl, 2-methyl-2-

propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, l-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, l-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, l-ethyl-2-propenyl, 2-ethyl-2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, l-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, l-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, l-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, and 4-methyl-4-pentenyl
The C2-C6 haloalkenyl represented by R6, R16, or R42 may include, for example, 3-chloro-2-propenyl, 3-bromo-2-propenyl, 2-chloro-2-propenyl, 2-bromo-2-propenyl, 3,3-dichloro-2-propenyl, 3,3-dibromo-2-propenyl, 3,3-di-fluoro-2-propenyl, 2,3-dichloro-2-propenyl, 2,3-dibromo-2-propenyl, 2-chloro-methyl-2-propenyl, 4-chloro-2-butenyl, 3-chloro-4,4,4-trifluoro-2-butenyl, 3-bromo-4,4,4-trifluoro-2-butenyl, 3,4-dichloro-4,4-difluoro-2-butenyl, 3,4,4, 4-tetrafluoro-3-butenyl, 4,4-dichloro-3-butenyl, 4,4-dibromo-3-butenyl, 5,5-dichloro-4-pentenyl, 5,5,-dibromO-4-pentenyl, 6,6-dichloro-5-hexenyl, and 6,6-dibormo-5-hexenyl
The C2-C6 alkynyl represented by R®, R^^, or R^^ may include, for example, 2-propynyl, 2-butynyl, 3-butynyl, l-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, l-methyl-2-butynyl, l-methyl-3-butynyl, 2-methyl-3-butynyl, l-ethyl-2-propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, l-ethyl-2-butynyl, l-ethyl-3-butynyl, and 2-ethyl-3-butynyL
The C3-C6 haloalkynyl represented by R6, R16, or R42 may include, for example, 3-chloro-2-propynyl, 3-bromo-2-propynyl, 4-chloro-2-butynyl, 4-chloro-3-butynyl, 4-bromo-2-butynyl, 4-bromo-3-butynyl, 5-chloro-4-pen-tynyl, 4-chloro-l-methyl-2-butynyl, 4-chloro-l-methyl-3-butynyl, 4-chloro-2-methyl-3-butynyl, 5-bromo-4-pentynyl, 4-bromo-l-methyl-2-butynyl, 4-bro-mo-l-methyl-3-butynyl, 4-bromo-2-methyl-3-butynyl, 6-chloro-5-hexynyl, and 6-bromo-5-hexynyl

The C2-C6 alkenyl R8 R9 R10 R15, R17 or R18 may include, for example, vinyl, 1-propenyl, isopropenyl, 1-butenyl, allyl, 2-butenyl, 3-butenyl, 1-meth-yl-2-propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, l-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, l-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, l-ethyl-2-propenyl, 2-ethyl-2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, l-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, l-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, l-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, and 4-methyl-4-pentenyL
The C2-C6 haloalkenyl represented by R8 R9 R10 R17 or R18 may include, for example, 2-chloroethenyl, 2-bromoethenyl, 2,2-dichloroethenyl, 2,2-dibromoethenyl, 3-chloro-2-propenyl, 3-bromo-2-propenyl, 2-chloro-2-pro-penyl, 2-bromo-2-propenyl, 3,3-dichloro-2-propenyl, 3,3-dibromo-2-propenyl, 3,3-difluoro-2-propenyl, 2,3-dichloro-2-propenyl, 2,3-dibromo-2-propenyl, 2-chloromethyl-2-propenyl, 4-chloro-2-butenyl, 3-chloro-4,4,4-trifluoro-2-bu-tenyl, 3-bromo-4,4,4-trifluoro-2-butenyl, 3,4-dichloro-4,4-difluoro-2-butenyl, 3,4,4,4-tetrafluoro-2-butenyl, 4,4-dichloro-3-butenyl, 4,4-dibromo-3-butenyl, 5,5-dichloro-4-pentenyl, 5,5-dibromo-4-pentenyl, 6,6-dichloro-5-hexenyl, and 6,6-dibromo-5-hexenyL
The C2-C6 alkynyl represented by R8 ,R9 R10 R17 or R18 may include, for example, ethynyl, 1-propynyl, 1-butynyl, 2-propynyl, 2-butynyl, 3-butynyl, l-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, l-methyl-2-butynyl, l-methyl-3-butynyl, 2-methyl-3-butynyl, l-ethyl-2-propynyl, 2-hexynyl, ^ 3-hexynyl, 4-hexynyl, 5-hexynyl, l-ethyl-2-butynyl, l-ethyl-3-butynyl, and 2-methyl-3-butynyl.
The C2-C6 haloalkynyl represented by R8 ,R9 R10, R17 or R18 may include, for example, 2-chloroethynyl, 2-bromoethynyl, 3-chloro-2-propynyl,

3-bromo-2-propynyl, 4-chloro-2-butynyl, 4-chloro-3-butynyl, 4-bromo-2-buty-nyl, 4-bromo-3-butynyl, 5-chloro-4-pentynyl, 4-chloro-l-methyl-2-butynyl, 4-chloro-l-methyl-3-butynyl, 4-chloro-2-methyl-3-butynyl, 5-bromo-4-pen-tynyl, 4-bromo-l-methyl-2-butynyl, 4-bromo-l-methyl-3-butynyl, 4-bromo-2-methyl-3-butynyl, 6-chloro-5-hexynyl, and 6-bromo-5-hexynyL
The C2-C6 cycloalkyl represented by R7 R15 R16 R17', or R42 may include cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl.
The C2-C10 alkoxyalkyl represented by R8 or R9 may include, for example, methoxymethyl, ethoxymethyl, n-propyloxymethyl, isopropyl-oxymethyl, 2-methoxyethyl, 1-methoxyethyl, 2-ethoxyethyl, 1-ethoxyethyl, 3-methoxypropyl, 2-methoxypropyl, l-methoxyp)ropyl, 2-methoxy-l-methyl-ethyl, 2-propyloxyethyl, 2-isopropyloxyethyl, 2-ethoxypropyl, 2-ethoxy-l-methylethyl, 2-methoxybutyl, l-ethyl-2-methoxyethyl, 3-ethoxypropyl, 3-methoxybutyl, 3-methoxy-2-methylpropyl, 3-methoxy-1-methylpropyl, 2-butoxyethyl, 3-methoxy-3-methylbutyl, and 2-butoxy-l-methylethyl.
The C2-C10 alkylthioalkyl represented by R8 or R9 may include, for example, methylthiomethyl, ethylthiomethyl, propylthiomethyl, isopropyl-thiomethyl, 2-methylthiomethyl, 1-methylthioethyl, 2-ethylthioethyl, 1-ethylthioethyl, 3-methylthiopropyl, 2-methylthiopropyl, 1-methylthiopro-pyl, 2-methylthio-l-methylethyl, 2-propylthioethyl, 2-isopropylthioethyl, 2-ethylthiopropyl, 2-ethylthio-l-methylethyl, 2-methylthiobutyl, l-ethyl-2-methylthioethyl, 3-ethylthiopropyl, 3-methylthiobutyl, 2-methyl-3-methyl-thiopropyl, l-methyl-3-methylthiopropyl, 4-methylthiobutyl, l-methyl-2-methylthiopropyl, 2-isobutylthioethyl, 2-sec-butylthioethyl, 3-isobutylthio-propyl, and 3-sec-butylthiopropyl.
The C2-C6 alkenyloxy represented by R10, R17, or R18 may include, for example, allyloxy, 2-butenyloxy, 3-butenyloxy, l-methyl-2-propenyloxy, 2-methyl-2-propenyloxy, 2-pentenyloxy, 3-pentenyloxy, 4-pentenyloxy,

l-methyl-2-butenyloxy, 2-methyl-2-butenyloxy, 3-methyl-2-butenyloxy, l-inethyl-3-butenyloxy, 2-methyl-3-butenyloxy, 3-methyl-3-butenyloxy, l-ethyl-2-propenyloxy, 2-ethyl-2-propenyloxy, 2-hexenyloxy, 3-hexenyloxy, 4-hexenyloxy, 5-hexenyloxy, l-methyl-2-pentenyloxy, 2-methyl-2-pentenyloxy, 3-methyl-2-pentenyloxy, 4-methyl-2-pentenyloxy, l-methyl-3-pentenyloxy, 2-methyl-3-pentenyloxy, 3-methyl-3-pentenyloxy, 4-methyl-3-pentenyloxy, l-methyl-4-pentenyloxy, 2-methyl-4-pentenyloxy, 3-methyl-4-pentenyloxy, and 4-methyl-4-pentenyloxy.
The C2-C6 haloalkenyloxy represented by R10, R17, or R18 may include, for example, 3-chloro-2-propenyloxy, 3-bromo-2-propenyloxy, 2-chloro-2-pro-penyloxy, 2-bromo-2-propenyloxy, 3,3-dichloro-2-propenyloxy, 3,3-dibromo-2-propenyloxy, 3,3-difluoro-2-propenyloxy, 2,3-dichloro-2-propenyloxy, 2,3-di-bromo-2-propenyloxy, 2-chloromethyl-2-propenyloxy, 4-chloro-2-butenyloxy, 3-chloro-4,4,4-trifluoro-2-butenyloxy, 3-bromo-4,4,4-trifluoro-2-butenyloxy, 3,4-dichloro-4,4-difluoro-2-butenyloxy, 3,4,4,4-tetrafluoro-2-butenyloxy, 4,4-dichloro-3-butenyloxy, 4,4-dibromo-3-butenyloxy, 5,5-dichloro-4-pentenyloxy, 5,5-dibromo-4-pentenyloxy, 6,6-dichloro-5-hexenyloxy, and 6,6-dibrmo-5-hexenyloxy.
The C2-C6 alkynyloxy represented by R10, R17 or R18 may include, for example, 2-propynyloxy, 2-butynyloxy, 3-butynyloxy, l-methyl-2-propynyloxy, 2-pentynyloxy, 3-pentynyloxy, 4-pentynyloxy, l-methyl-2-butynyloxy, l-methyl-3-butynyloxy, 2-methyl-3-butynyloxy, l-ethyl-2-propynyloxy, 2-hexynyloxy, 3-hexynyloxy, 4-hexynyloxy, 5-hexynyloxy, l-ethyl-2-butynyl-oxy, l-ethyl-3-butynyloxy, and 2-ethyl-3-butynyloxy.
The C2-C6 haloalkynyloxy represented by R10, R17, or R18 may include, for example, 3-chloro-2-propynyloxy, 3-bromo-2-propynyloxy, 4-chloro-2-butynyloxy, 4-chloro-3-butynyloxy, 4-bromo-2-butynyloxy, 4-bromo-3-buty-nyloxy, 5-chloro-4-pentynyloxy, 4-chloro-l-methyl-2-butynyloxy, 4-chloro-l-

inethyl-3-butynyloxy, 4-chloro-2-inethyl-3-butynyloxy, 5-bromo-4-pentynyl-oxy, 4-broino-l-inethyl-2-butynyloxy, 4-bromo-l-methyl-3-butynyloxy, 4-bro-mo-2-methyl-3-butynyloxy, 6-chloro-5-hexynyloxy, and 6-bromo-5-hexynyl-oxy.
The (C1-C3 alkoxy)carbonyl represented by R10 may include, for example, methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, isopropyl-oxycarbonyl, n-butyloxycarbonyl, isobutyloxycarbonyl, sec-butyloxycarbonyl, tert-butyloxycarbonyl, n-pentyloxycarbonyl, isopentyloxycarbonyl, neopen-tyloxycarbonyl, tert-pentyloxycarbonyl, and 1-ethylpropyloxycarbonyl.
The C1-C3 alkylthio represented by R17- or R18 may include methylthio, ethylthio, propylthio, and isopropylthio.
The C1-C3 haloalkylthio represented by R17 or R18 may include, for example, trifluoromethylthio, difluoromethylthio, bromodifluoromethylthio, 2,2,2-trifluoroethylthio, 2-chloro-l,l,2-trifluoroethylthio, 2-bromo-l,l,2-tri-fluoroethylthio, 1,1,2,2-tetrafluoroethylthio, 2-chloroethylthio, 2-fluoroethyl-thio, 2-bromoethylthio, 1,1,2,2,2-pentafluoroethylthio, 3-fluoropropylthio, 3-chloropropylthio, 3-bromopropylthio, 2,2,3,3,3-pentafluoropropylthio, and 3,3,3-trifluoropropylthio.
The C1-C2 alkylsulfinyl represented by R17 or R18 may include methylsulfinyl or ethylsulfinyl.
The C1-C2 alkylsulfonyl represented by R17 or R18 may include methylsulfonyl and ethylsulfonyl.
The C1-C2 haloalkylsulfinyl represented by R17 or R18 may include, for example, trifluoromethylsulfinyl, 2,2,2-trifluoroethylsulfinyl, and perfluoro-ethylsulfinyl.
The C1-C2 haloalkylsulfonyl represented by R17 or R18 may include, for example, trifluoromethylsulfonyl, 2,2,2-trifluoroethylsulfonyl, and perfluoro-ethylsulfonyl.

The C1-C3 hydroxyalkyl represented by R17 or R18 may include hydroxymethyl, 2-hydroxyethyl, and 3-hydroxypropyl.
The C2-C4 alkoxyalkyl represented by R17 or R18 may include, for example, methoxymethyl, ethoxymethyl, propyloxymethyl, isopropyloxy-methyl, 2-methoxyethyl, 1-methoxyethyl, 2-ethoxyethyl, 1-ethoxyethyl, 3-methoxypropyl, 2-methoxypropyl, 1-methoxypropyl, and 2-methoxy-l-methylethyl.
The C2-C4 alkylthioalkyl represented by R17 or R18 may include, for
example, methylthiomethyl, ethylthiomethyl, propylthiomethyl, isopropyl-
' thiomethyl, 2-methylthioethyl, 1-methylthioethyl, 2-ethylthioethyl, 1-ethyl-
thioethyl, 3-methylthiopropyl, 2-methylthiopropyl, 1-methylthiopropyl, and
2-methylthio-l-methylethyl.
The (C1-C2 alkyl)aminocarbonyl represented by R17 may include methylaminocarbonyl or ethylaminocarbonyl.
The di(Ci-C2 alkyl)aminocarbonyl represented by R^*^ may include dimethylaminocarbonyl, N-methyl-N-ethylaminocarbonyl, or diethylamino-carbonyl.
The (C1-C6 alkoxy)carbonyl represented by R17 may include, for example, methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, isopropyl- oxycarbonyl, n-butyloxycarbonyl, isobutyloxycarbonyl, sec-butyloxycarbonyl, tert-butyloxycarbonyl, n-pentyloxycarbonyl, isopentyloxycarbonyl, neopen-tyloxycarbonyl, tert-pentyloxycarbonyl, 1-ethylpropyloxycarbonyl, n-hexyl-oxycarbonyl, isohexyloxycarbonyl, 2-ethylbutyloxycarbonyl, 1-methylpentyl-oxycarbonyl, 1-ethylbutyloxycarbonyl, 3-methylpentyloxycarbonyl, and 1,3-dimethylbutylcarbonyl.
The C2-C6 cycloalkenyl represented by R17 may include 1-cyclopen-tenyl, 2-cyclopentenyl, 3-cyclopentenyl, 1-cyclohexenyl, 2-cyclohexenyl, or 3-cyclohexenyl

The C2-C6 cycloalkyloxy represented by R17 may include cyclopropyl-oxy, cyclobutyloxy, cyclopentyloxy, or cyclohexyloxy.
The C5-C6 cycloalkenyloxy represented by R1 may include 1-cyclo-pentenyloxy, 2-cyclopentenyloxy, 3-cyclopentenyloxy, 1-cyclohexenyloxy, 2-cyclohexenyloxy, or 3-cyclohexenyloxy.
The 3,3-dihalogeno-substituted-2-propenyl represented by R4 may include, for example, 3,3-dichloro-2-propenyl, 3,3-dibromo-2-propenyl, 3-bro-mo-3-chloro-2-propenyl, 3-chloro-3-fluoro-2-propenyl, and 3-bromo-3-fluoro-2-propenyL
The C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, which is represented by R6, R8, or R9, may include, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 2-methylcyclopentyl, 3-methylcyclopentyl, 2-methyl-cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 4-ethylcyclohexyl, 4-n-propylcyclohexyl, 4-isopropylcyclohexyl, and 4-tert-butylcyclohexyl
The C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, which is represented by R6, R8, or R9, may include, for example, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclo-hexylmethyl, 1-cyclopropylethyl, (2-methylcyclopropyl)methyl, 2-(2-methyl-cyclopropyl)ethyl, 2-cyclopentylethyl, 3-cyclopentylpropyl, 2-cyclohexylethyl, and 3-cyclohexylpropyl.
The C3-C6 cycloalkenyl optionally substituted with C1-C4 alkyl, which is represented by R6, R8, or R9, may include, for example, 2-cyclopentenyl, 3-cyclopentenyl, 2-cyclohexenyl, 3-cyclohexenyl, 3,5,5-trimethyl-2-cyclo-hexenyl, and 3-methyl-2-cyclohexenyl.
The C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof, which is represented by R6, R8, or R9, may include, for example, (l-cyclopentenyl)methyl, (2-cyclopentenyl)methyl, (1-cyclohexenyl)-methyl, (2-cyclohexenyl)methyl, (3-cyclophexenyl)methyl, and 2-(3-cyclo-

n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, and isobutyl.
The C1-C3 haloalkyl in the phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy, which is represented by R7 R15, R16, R17, R18, or R42, may include, for example, trifluo-romethyl, difluoromethyl, bromodifluoromethyl, 1-fluoroethyl, 1-chloroethyl, 1-bromoethyl, perfluoroethyl, 2-bromo-l,l,2,2-tetrafluoroethyl, 1,1,2,2-tetra-fluoroethyl, 2-chloro-l,l,2-trifluoroethyl, 2-bromo-l,l,2-trifluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, 2-fluoroethyl, 2-chlo-roethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoropropyl, l,l,l,3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bromopropyl, 2-iodopropyl, and 2,3-dibromopropyl.

romethoxy, bromodifluoromethoxy, 1-fluoroethoxy, 1-chloroethoxy, 1-bromo-ethoxy, perfluoroethoxy, 2-bromo-l,l>2,2-tetrafliioroethoxy, 1,1,2,2-tetrafluo-roethoxy, 2-chloro-l,l,2-trifluoroethoxy, 2-bromo-l,l,2-trifluoroethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy, 2,2,2-tribromoethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2-dichloro-ethoxy, 2,2-dibromoethoxy, 3-fluoropropyloxy, 3-chloropropyloxy, 3-bromo-propyloxy, 3-iodopropyloxy, 3,3,3-trifluoropropyloxy, 2,2,2,3,3,3-hexafluoro-propyloxy, l,l,l,3,3,3-hexafluoro-2-propyloxy, 2-fluoropropyloxy, 2-chloropro-pyloxy, 2-bromopropyloxy, 2-iodopropyloxy, and 2,3-dibromopropyloxy.
The halogen in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R7, R16, R17, or R42, may include fluorine, chlorine, bromine, or iodine.
The C1-C4 alkyl in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R7, R16, R17, or R42, may include methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, and isobutyl.
The C1-C3 haloalkyl in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring ' thereof, which is represented by R7, R16, R17, or R42, may include, for example, trifluoromethyl, difluoromethyl, bromodifluoromethyl, 1-fluoroethyl, 1-chloroethyl, 1-bromoethyl, perfluoroethyl, 2-bromo-l,l,2,2-tetrafluoroethyl, 1,1,2,2-tetrafluoroethyl, 2-chloro-l,l,2-trifluoroethyl, 2-bromo-l,l,2-trifluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, - 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoro-propyl, l,l,l,3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bro-

mopropyl, 2-iodopropyl, and 2,3-dibromopropyl.
The C1-C3 alkoxy in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R7, R16, R17 or R42, may include methoxy, ethoxy, n-propyloxy, or isopropyloxy
The C1-C3 haloalkoxy in the benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R7, R16, R17, or R42, may include, for example, trifluoromethoxy, bromodifluoromethoxy, 1-fluoroethoxy, 1-chlo-roethoxy, 1-bromoethoxy, perfluoroethoxy, 2-bromo-l,l,2,2-tetrafluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-chloro-l,l,2-trifluoroethoxy, 2-bromo-l,l,2-tri-luoroethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy, 2,2,2-tribromo-ethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-di-fluoroethoxy, 2,2-dichloroethoxy, 2,2-dibromoethoxy, 3-fluoropropyloxy, 3-chloropropyloxy, 3-bromopropyloxy, 3-iodopropyloxy, 3,3,3-trifluoropro-pyloxy, 2,2,2,3,3,3-hexafluoropropyloxy, 1,1,1,3,3,3-hexafluoro-2-propyloxy, 2-fluoropropyloxy, 2-chloropropyloxy, 2-bromopropyloxy, 2-iodopropyloxy, and 2,3-dibormopropyloxy.
The halogen in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R17, may include fluorine, chlorine, bromine, or iodine.
The C1-C4 alkyl in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R17, may include methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, and isobutyl.
The C1-C3 haloalkyl in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 halo-

alkoxy on the ring thereof, which is represented by R17, may include, for example, trifluoromethyl, difluoromethyl, bromodifluoromethyl, 1-fluoro-ethyl, 1-chloroethyl, 1-bromoethyl, perfluoroethyl, 2-bromo-l,l,2,2-tetra-fluoroethyl, 1,1,2,2-tetrafluoroethyl, 2-chloro-l,l,2-trifluoroethyl, 2-bromo- 1,1,2-trifluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromo-ethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoro-ethyl, 2,2-dichloroethyl, 2,2-dibromoethyl, 3-fluoropropyl, 3-chloropropyl, 3-bromopropyl, 3-iodopropyl, 3,3,3-trifluoropropyl, 2,2,2,3,3,3-hexafluoro-propyl, l,l,l,3,3,3-hexafluoro-2-propyl, 2-fluoropropyl, 2-chloropropyl, 2-bro-mopropyl, 2-iodopropyl, and 2,3-dibromopropyL
The C1-C3 alkoxy in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R17 may include methoxy, ethoxy, n-propyloxy, or isopropyloxy.
The C1-C3 haloalkoxy in the phenoxy or benzyloxy optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof, which is represented by R17, may include, for example, trifluoromethoxy, bromodifluoromethoxy, 1-fluoroethoxy, 1-chloroethoxy, 1-bromoethoxy, perfluoroethoxy, 2-bromo-l,l,2,2-tetrafluoro-ethoxy, 1,1,2,2-tetrafluoroethoxy, 2-chloro-l,l,2-trifluoroethoxy, 2-bromo-1,1,2-trifluoroethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy, 2,2,2-tri-bromoethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2-dichloroethoxy, 2,2-dibromoethoxy, 3-fluoropropyloxy, 3-chloropropyloxy, 3-bromopropyloxy, 3-iodopropyloxy, 3,3,3-trifluoropropyl-oxy, 2,2,2,3,3,3-hexafluoropropyloxy, l,l,l,3,3,3-hexafluoro-2-propyloxy, 2-fluoropropyloxy, 2-chloropropyloxy, 2-bromopropyloxy, 2-iodopropyloxy, and 2,3-dibormopropyloxy.
The halogen in the methylenedioxy optionally substituted with

halogen or C1-C3 alkyl, which is represented by R17 and which is formed from two adjacent R17's combined together at their ends when b is 2 to 5, may include fluorine, chlorine, bromine, or iodine.
The C1-C3 alkyl in the methylenedioxy optionally substituted with
halogen or C1-C3 alkyl, which is represented by R17 and which is formed from two adjacent R17's combined together at their ends when b is 2 to 5, may include methyl, ethyl, n-propyl, and isopropyl.
The halogen in the ethylenedioxy optionally substituted with halogen or C1-C4 alkyl, which is represented by R17 and which is formed from two
' adjacent R17's combined together at their ends when b is 2 to 5, may include fluorine, chlorine, bromine, or iodine.
The C1-C3 alkyl in the ethylenedioxy optionally substituted with halogen or C1-C3 alkyl, which is represented by R17 and which is formed from two adjacent R17's combined together at their ends when b is 2 to 5, may
- include methyl, ethyl, n-propyl, and isopropyl.
R8 and R9, when combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring thereof, represent tetramethylene optionally substituted with C1-C4 alkyl or halogen; pentamethylene optionally substituted
■ with C1-C4 alkyl or halogen; butenylene optionally substituted with C1-C4 alkyl or halogen; pentenylene optionally substituted with C1-C4 alkyl or halogen; or pentadienylene optionally substituted with C1-C4 alkyl or halogen; examples of which are tetramethylene, 1-methyltetramethylene, 2-methyltetramethylene, 1,1-dimethyltetramethylene, 1,3-dimethyltetra-methylene, pentamethylene, 1-methylpentamethylene, 2-methylpentameth-ylene, 3-methylpentamethylene, 3-ethylpentamethylene, 3-tert-butylpenta-methylene, 1,1-dimethylpentamethylene, 1,5-dimethylpentamethylene, 1-chloropentamethylene, 1-methoxypentamethylene, 1-butenylene,

1-methyl-l-butenylene, 2-methyl-l-butenylene, 1-pentenylene, 2-methyl-l-pentenylene, 3,3-dimethyl-l-pentenylene, 2-oxa-l-methyltetramethylene, 3-oxapentamethylene, 3-oxa-l,4-pentadienylene, 2-thiatetramethylene, 3-thiapentainethylene, 3,3-dimethyl-2,4-dioxapentainethylene, and 2,4-dithiapentamethylene. In these groups, each methylene or methine linkage may be replaced with an oxygen or sulfur atom.
The C2-C6 cycloalkylene represented by E may include 1,2-cyclo-hexylene, 1,3-cyclohexylene, 1,4-cyclohexylene, 1,2-cyclopentylene, and 1,3-cyclopentylene.
The C1-C3 alkyl substituted with cyano, nitro, (C1-C4 alkoxy)carbonyl, C1-C4 alkylthio, or C1-C4 alkoxy, which is represented by R6, may include, for example, cyanomethyl, 1-cyanoethyl, 2-cyanoethyl, 3-cyanopropyl, nitro-methyl, 1-nitroethyl, 1-methyl-l-nitroethyl, methoxycarbonylmethyl, ethoxy-carbonylmethyl, isopropoxycarbonylmethyl, l-(methoxycarbonyl)ethyl, 2-(methoxycarbonyl)ethyl, methoxymethyl, ethoxymethyl, 1-methoxyethyl, 2-methoxyethyl, 2-ethoxyethyl, 2,2-dimethoxyethyl, 2,2-diethoxyethyl, 2,2-dimethoxypropyl, 2,2-diethoxypropyl, 3,3-dimethoxypropyl, 3,3-diethoxy-propyl, 2,3-dimethoxypropyl, methylthiomethyl, 2-methylthioethyl, and 2,2-di(methylthio)ethyL
In the case where h is 0 and i is 1 in A1-1, R22 and R7, when combined together at their ends to form trimethylene, tetramethylene, or penta-methylene, which is optionally substituted with C1-C3 alkyl, may include, for example, trimethylene, 1-methyltrimethylene, 2-methyltrimethylene, tetramethylene, 1-methyltetramethylene, 2-methyltetramethylene, and penta-methylene.
In the case where h is 0 and j is 1 in A1-2, A1-3, A1-4, A1-5, or A1-6, R22 and R7, when combined together at their ends to form trimethylene, tetramethylene, or pentamethylene, which is optionally substituted with C1-C3

alkyl, may include, for example, trimethylene, 1-methyltrimethylene, 2-methyltrimethylene, tetramethylene, 1-methyltetramethylene, 2-methyl-tetramethylene, and pentamethylene.
Preferred examples of the present compounds are as follows:
oxime compounds of formula (1) wherein X is X1;
oxime compounds of formula (1) wherein X is X1 and A1 is A1-1, A1-2, A1-3,A1-4,,A1-5, or A1-6;

or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl,
or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof,
or C5-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C6-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof;
oxime compounds of formula (1) wherein X is X1 R7 is hydrogen,
C1-C6 alkyl, or C1-C3 haloalkyl,

oxime compounds of formula (1) wherein X is X1 R7 is hydrogen, C1-C6 alkyl, or C1-C3 haloalkyl,
A1 is A1-3, or A1 is A1-2 and k is an integer of 2 to 6,
Q1 is oxygen, and
R6 is C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, C2-C6 haloalkenyl, C3-C6 alkynyl, or Cg-Ce haloalkynyl,
or Cg-C, cycloalkyl optionally substituted with C1-C4 alkyl,
or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof,
or C5-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C3-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on

the ring thereof,
or T1-l or T1-2;
oxime compounds of formula (1) wherein R2 and R3 are independently chlorine or C1-C3 alkyl,
a is 0,
R4 is 3,3-dichloro-2-propenyl or 3,3-dibromo-2-propenyl,

R4 is 3,3-dichloro-2-propenyl,
R6 is isopropyl, isobutyl, sec-butyl, tert-butyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl, l,l,l,3,3,3-hexafluoro-2-propyl, or 3,3-dichloro-2-propenyl, and
R7 is hydrogen;
oxime compounds of formula (1) wherein X is X1
A1 is A1-2, R21 R22 R23 and R24 are all hydrogen, h is 0, Q1 is oxygen, j is 1, k is an integer of 3 to 6,
Y and Z are both oxygen,

W is a benzene ring, a heterocyclic 6-membered ring containing at least oxygen, sulfur, or nitrogen atom, a heterocyclic 5-membered ring containing at least one oxygen, sulfur, or nitrogen atom, or any one of these rings substituted with one to four identical or different (R40)g2's, wherein R40 is halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy, and g2 is an integer of 1 to 4;
oxime compounds of formula (1) wherein A1 is A1-7, A1-8, A1-9, A1-10, A1.ll,or A1-12, and

W is a benzene ring, a pyridine ring, a pyridazine ring, a pyrimidine ring, a pyradine ring, a furan ring, a thiophene ring, a pyrrole ring, an oxazole ring, an isoxazole ring, a thiazole ring, an isothiazole ring, a pyrazole ring, an imidazole ring, or any one of these rings substituted with one to four identical or different (R40)g2's;
oxime compounds of formula (1) wherein A1 is A1-7, A1-8, A1-9, A1-10, A1-ll, or A1-12, and
W is a benzene ring, a pyridine ring, a pyridazine ring, or any one of

oxime compounds of formula (1) wherein X is X2;
oxime compounds of formula (1) wherein X is X2, and Y and Z are both oxygen;
oxime compounds of formula (1) wherein X is X2 and a is 0;
oxime compounds of formula (1) wherein X is X2, and R1 R2, and R3 are independently halogen or C1-C3 alkyl;
oxime compounds of formula (1) wherein A2 is A2-1;
oxime compounds of formula (1) wherein A2 is A2-2 and Q1 is oxygen;
oxime compounds of formula (1) wherein A2 is A2-3 and Q2 is oxygen;
oxime compounds of formula (1) wherein A2 is A2--4, and Q2 and Q3 are

or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof,
or C5-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C6-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on

or a heterocyclic 6-membered ring, exclusive of pyridine ring, containing at least one oxygen, sulfur, or nitrogen atom, which heterocyclic 6-membered ring may be optionally substituted with one to three identical or different (R18)g's, and R18 and g are as defined above,
or a heterocyclic 5-membered ring containing at least one oxygen, sulfur, or nitrogen atom, which heterocyclic 5-membered ring may be optionally substituted with one to three identical or different (R18)g's, and R18 and g are as defined above,
or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring thereof;
oxime compounds of formula (1) wherein X is X2, and R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C2-C10 alkoxyalkyl, C2-C10 alkylthioalkyl, or naphthyl,
or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl, or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on the ring thereof,
or C2-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on

wherein R17, D, R11 R12, b, and d are as defined above,
or 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, or 3-pyrrolyl, each
of which heterocyclic groups may be optionally substituted with one to three
identical or different (R18) wherein R18 and g are as defined above,
or R8 and R9 are combined together at their ends to form a saturated
or unsaturated 5- or 6-membered ring containing zero to two oxygen or
sulfur atoms in the ring thereof;
oxime compounds of formula (1) wherein X is X2, and
R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C3 haloalkyl,
C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C3-C6 haloalkynyl, C2-C10
alkoxyalkyl, or C2-C10 alkylthioalkyl,
or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl,
or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof,
or C2-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof,
or T2-1 or T2-2 of formula (4)
T2.I T2.2

wherein R17, D, R11 R12, b, and d are as defined above,
or R8 and R9 are combined together at their ends to form a saturated
or unsaturated 5- or 6-membered ring containing zero to two oxygen or
sulfur atoms in the ring thereof;
oxime compounds of formula (1) wherein X is X2, and
R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C3 haloalkyl,
C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C3-C6 haloalkynyl, C2-C10
alkoxyalkyl, or C2-C10 alkylthioalkyl,
or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl,
or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof,
or C2-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C6-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof,
or R8 and R9 are combined together at their ends to form a saturated
or unsaturated 5- or 6-membered ring containing zero to two oxygen or
sulfur atoms in the ring thereof; and
oxime compounds of formula (1) wherein X is X2, and
R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C3 haloalkyl,
C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C2-C10
alkoxyalkyl, or C2-C10 alkylthioalkyl,
or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl,
or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof,
or C3-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C2-C6 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof.
Particularly preferred examples of the present compounds are as

follows:
(187) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-
nal 0-isopropyloxime
(169) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-
nal 0-isopropyIoxime
(188) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-
nal 0-isopropyloxime
(26) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-nal 0-tert-butyloxime
(16) 5-(2,6-dicliloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-
nal 0-tert-butyloxime
(134) 6-(2,6-dicliloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-tert-butyloxime
(189) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-
nal 0-(2,2,2-trichloroethyl)oxime
(170) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-
nal 0-(2,2,2-trichloroethyl)oxime
(190) 6-(2,6-dicliloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-
nal 0-(2,2,2-trichloroethyl)oxime
(24) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-nal 0-(3,3-dichloro-2-propenyl)oxime
(17) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-
nal 0-(3,3-dichloro-2-propenyl)oxime
(76) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-(3,3-dichloro-2-propenyl)oxime
(165) 4-(2,6-diehloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-isopropyloxime
(152) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-

oxyacetaldehyde 0-isopropyloxime
(191) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-
oxyacetone 0-isopropyloxime
(172) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl
oxyacetone 0-isopropyloxime
(6) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-
oxyacetaldehyde 0-tert-butyloxime
(14) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-
oxyacetaldehyde 0-tert-butyloxime
(103) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-tert-butyloxime
(104) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-tert-butyloxime
(167) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime
(160) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime
(192) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-
oxyacetone 0-(2,2,2-trichloroethyl)oxime
(173) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-
oxyacetone 0-(2,2,2-trichloroethyl)oxime
(2) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-
oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(15) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-
oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(46) 4-(2,6-dichloro-4-(3,3-dichIoro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(47) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-

oxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(329) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-ylbenzaldehyde 0-sec-butyloxime
(314) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-
ylbenzaldehyde 0-t-butyloxime
(355) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-sec-butyloxime
(357) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-allyloxime
(358) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxiine

(338) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-n-propyloxime
(339) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-isopropyloxime
(340) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde O-sec-butyloxime
(291) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-t-butyloxime
(293) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-ethyloxime
(318) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propiophenone 0-ethyloxime
(297) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-ethyloxime
(310) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-n-propyloxime
(315) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-

tyloxy)benzaldehyde 0-isopropyloxime
(391) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-2,2,2-trifluoroacetophenone 0-ethyloxime
(529) 4-(trifluoromethyl)benzaldehyde 0-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime
(531) 4'-(trifluoromethyl)acetophenone 0-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime
(545) trimethylacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(559) 3,3-dimethyl-2-butanoneO-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(562) 3,3-dimethyl-2-butanone O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(563) 4-methyl-2-pentanone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(564) 4-methyl-2-pentanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(582) 3-methyl-2-butanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime
The above numbers preceding the compound names are also used below for designating the present compounds.
The present compounds can be produced, for example, by the following production processes A to M.
Production process A (the compounds of formula (1) wherein X is X1 and R6 is hydrogen are excluded)
This is the production process in which a compound of formula (15)

wherein R4 is as defined above and L is halogen (e.g., chlorine, bromine, iodine), mesyloxy, or tosyloxy.
The reaction is preferably effected in the presence of an appropriate base and in an inert solvent.
The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture.
The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as

sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (15).
The reaction temperature, although it can be usually selected in the range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of -5°C to the boiling point of the solvent used in the reaction or 100°C.
The molar ratio of the starting materials and base to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process B (for the present compounds wherein Y is oxygen, with the proviso that when X is X1 R6 is not hydrogen)
This is the production process in which the compound of formula (15) wherein Y is oxygen is reacted with an alcohol compound of formula (17)
HO-R4
wherein R4 is as defined above.
The reaction is preferably effected in the presence of an appropriate dehydrating agent and, if necessary, in an inert solvent.
The dehydrating agent which can be used may include, for example, dicyclohexylcarbodiimide, dialkyl (e.g., C1-C4) azodicarboxylate (e.g., diethyl-

azodicarboxylate, and diisopropylazodicarboxylate) - trialkyl (e.g., C1-C20) phosphine or triarylphosphine (e.g., triphenylphosphine, trioctylphosphine, tributylphosphine) systems.
The solvent which can be used may include, for example, hydro-' carbons such as benzene, xylene, and toluene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, and dioxane; and halogenated hydrocarbons such as carbon tetrachloride, dichloromethane, chlorobenzene, and dichlorobenzene.
The reaction temperature can be usually selected in the range of -20°C to 200°C or the boiling point of a solvent used in the reaction.
The molar ratio of the starting materials and base to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process C (for the present compounds wherein Y and Z are both oxygen, with the proviso that when X is X1 R6 is not hydrogen)
This is the production process in which a compound of formula (18)

wherein R1 R2, R3, R4 and a are as defined above, is reacted with a compound of formula (19)

wherein X and L are as defined above, with the proviso that when X is X1 R6 is hydrogen.
The reaction is preferably effected in the presence of an appropriate base and in an inert solvent.
The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture.
The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (18).
The reaction temperature, although it can be usually selected in the

range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of -5°C to the boiling point of the solvent used in the reaction or 100°C.
The molar ratio of the starting materials and base to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process D (for the present compounds wherein Y and Z are both oxygen, with the proviso that when X is X1 R6 is not hydrogen)
This is the production process in which a compound of formula (18) is reacted with a compound of formula (20)
X-OH
wherein X is as defined above, with the proviso that when X is X1 R6 is not hydrogen.
The reaction is preferably effected in the presence of an appropriate dehydrating agent and, if necessary, in an inert solvent.
The dehydrating agent which can be used may include, for example, dicyclohexylcarbodiimide, dialkyl (e.g., C1-C4) azodicarboxylate (e.g., diethyl-azodicarboxylate, and diisopropylazodicarboxylate) - trialkyl (e.g., C1-C20) phosphine or triarylphosphine (e.g., triphenylphosphine, trioctylphosphine, tributylphosphine) systems.
The solvent which can be used may include, for example, hydrocarbons such as benzene, xylene, and toluene; ethers such as diethyl ether,

diisopropyl ether, tetrahydrofuran, and dioxane; and halogenated hydrocarbons such as carbon tetrachloride, dichloromethane, chlorobenzene, and dichlorobenzene.
The reaction temperature can be usually selected in the range of -20°C to 200°C or the boiling point of a solvent used in the reaction.
The molar ratio of starting materials and dehydrating agent to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process E (for the present compounds wherein X is X1)
This is the production process in which a hydroxylamine compound of formula (21)
R6O-NH2
wherein R6 is as defined above, or a salt thereof, is reacted with a carbonyl compound of formula (22)

wherein R1 R2 R3, R4 R7 A1 Y, Z, and a are as defined above.
The reaction can be effected in an inert solvent and, if necessary, in the presence of a base or an acid.
The solvent which can be used may include, for example, alcohols

such as methanol and ethanol; ethers such as diethyl ether, tetrahydrofuran, and dioxane; acetic acid; and water. If necessary, these solvents may also be used in admixture.
The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. The amount of base to be used, if necessary, in the reaction is preferably 1 mole or more relative to 1 mole of the hydroxylamine compound of formula (21). The organic bases such as triethylamine and pyridine can serve both as the base and as the solvent, when the reaction is effected with them in large excess relative to the hydroxylamine compound of formula (21).
The acid which can be used may include, for example, hydrochloric acid, sulfuric acid, and p-toluenesulfonic acid. The acid can be used in the reaction at a catalytic amount ranging from 0.01 to 1 equivalent relative to the carbonyl compound of formula (22).
The hydroxylamine compound as the starting material, although it can be used as such in the reaction, is usually used in the form of an inorganic acid salt, such as hydrochloride or sulfate.
The reaction temperature, although it can be usually selected in the range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of 0°C to the boiling point of the solvent used in the reaction or 60°C.

The molar ratio of the starting materials and reagents to be used in the reaction may be freely selected; however, it is favorable that the reaction of the carbonyl compound of formula (22) and the hydroxylamine compound of formula (21) or a salt thereof is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process F (for the present compounds wherein X is X1 with the proviso that R6 is not hydrogen, T1-4, T1-5, T1-6, or T1-7)
This is the production process in which a compound of formula (23)

present compound wherein X is X1 and R6 is hydrogen).
The reaction is preferably effected in the presence of an appropriate base and in an inert solvent.
The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl

ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture.
The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0,01 to 1 mole relative to 1 mole of the compound of formula (24).
The reaction temperature, although it can be usually selected in the range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of -5°C to the boiling point of the solvent used in the reaction or 100°C.
The molar ratio of the starting materials and base to be used in the reaction may be freely selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If

necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process G (for the present compounds wherein Y and Z are both oxygen, X is X1 A^ is A1-8, and el is 0, with the proviso that R6 is not hydrogen)

wherein R6, R7, G1 and W are as defined above, Q4 is oxygen, sulfur, or NR39, and R39 is as defined above.
The reaction is preferably effected in the presence of an appropriate base and in an inert solvent.
The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may

also be used in admixture.
The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, sodium carbonate, potassium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (25).
The reaction temperature can be usually selected in the range of -20°C to the boiling point of a solvent used in the reaction or 150°C.
The molar ratio of the starting materials and base to be used in the reaction may be suitably selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process H (for the present compounds wherein Y and Z - are both oxygen, X is X2, A2 is A2-4, and el is 0)
This is the production process in which a compound of formula (27)

The reaction is preferably effected in the presence of an appropriate base and in an inert solvent.
The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as - toluene, benzene, and xylene; and water. If necessary, these solvents may

also be used in admixture.
The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, sodium carbonate, potassium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (27).
The reaction temperature can be usually selected in the range of -20°C to the boiling point of a solvent used in the reaction or 150°C.
The molar ratio of the starting materials and base to be used in the reaction may be freely selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process I (for the present compounds wherein X is X2)
This is the production process in which an 0-substituted hydroxyl-amine compound of formula (29)

the presence of a base.
The solvent which can be used may include, for example, alcohols such as methanol and ethanol; ethers such as diethyl ether, tetrahydrofuran, and dioxane; pyridine; and water. The carbonyl compound of formula (30) may also be used as the solvent. If necessary, these solvents may also be used in admixture.
The base which can be used may include, for example, triethylamine, pyridine, and sodium acetate.
The 0-substituted hydroxylamine compound as the starting material is usually used in the form of an inorganic acid salt such as hydrochloride.
The reaction temperature is usually in the range of 0°C to 150°C.
The molar ratio of the starting materials and reagents to be used in the reaction may be suitably selected; however, it is preferred that the reaction of the carbonyl compound of formula (30) and the 0-substituted hydroxylamine compound of formula (29) or a salt thereof is effected at the equimolar ratio or a ratio close thereto. The amount of base to be used, if

necessary, in the reaction is preferably 1 mole or more relative to 1 mole of the compound of formula (29).
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process J (for the present compounds wherein X is X2) This is the production process in which a compound of formula (31)

The reaction is preferably effected in the presence of an appropriate base and in an inert solvent.
The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile,

and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture.
The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, sodium carbonate, potassium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-C4) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In necessary, catalysts such as ammonium salts (e.g., triethylbenzylammonium chloride) may be added to the reaction system in an amount of 0.01 to 1 mole relative to 1 mole of the compound of formula (31).
The reaction temperature can be usually selected in the range of -20°C to the boiling point of a solvent used in the reaction or 150°C.
The molar ratio of the starting materials and base to be used in the reaction may be freely selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process K (for the compounds wherein X is X1 and R6 is T1-4, T1-5, or T1-7)

wherein R15 and L1 are as defined above (when R6 is T1-7), is reacted with a compound of formula (24).
The reaction is preferably effected in the presence of an appropriate base and in an inert solvent.
The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl

ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; hydrocarbons such as toluene, benzene, and xylene; and water. If necessary, these solvents may also be used in admixture.
The base which can be used may include hydroxides of alkali metals or alkaline earth metals, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, and calcium hydroxide; carbonates of alkali metals or alkaline earth metals, such as lithium carbonate, potassium carbonate, sodium carbonate, and calcium carbonate; hydrides of alkali metals or alkaline earth metals, such as lithium hydride, sodium hydride, potassium hydride, and calcium hydride; alkoxides (e.g., C1-04) of alkali metals, such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide; and organic bases such as triethylamine and pyridine. In particular, organic bases such as triethylamine or pyridine are preferably used.
The reaction temperature, although it can be usually selected in the range of-20°C to the boiling point of a solvent used in the reaction or 150°C, is more preferably in the range of -5°C to the boiling point of the solvent used in the reaction or 50°C.
The molar ratio of the starting materials and base to be used in the reaction may be freely selected; however, it is favorable that the reaction is effected with the compound of formula (33), (34), (35), or (36) and the base in an amount of 1 to 5 moles, respectively, relative to 1 mole of the compound of formula (24).
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If

necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process L (for the present compounds wherein X is X1 and R6 is T1-G)
This is the production process in which an isocyanate compound or an isothiocyanate compound of formula (37)
wherein J and R16 are as defined above, is reacted with a compound of formula (24).
The reaction is effected, if necessary, in the presence of an appropriate catalyst and in an inert solvent.
The solvent which can be used may include ketones such as acetone, methyl ethyl ketone, and cyclohexanone; ethers such as 1,2-dimethoxy-ethane, tetrahydrofuran, dioxane, and dialkyl (e.g., C1-C4) ether (e.g., diethyl ether, diisopropyl ether); polar solvents such as N,N-dimethylformamide, dimethylsulfoxide, hexamethylphosphoric triamide, sulforane, acetonitrile, and nitromethane; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; and hydrocarbons such as toluene, benzene, and xylene. If necessary, these solvents may also be used in admixture.
As the catalyst, for example, bases such as triethylamine, pyridine, and sodium acetate, or acids such as aluminum chloride, hydrogen chloride, and boron trifluoride ether complex (BF3.(C2H5)20), can be used.
The reaction temperature, although it can be usually selected in the range of -20°C to the boiling point of a solvent used in the reaction, is more preferably in the range of-5°C to the boiling point of the solvent used in the

reaction.
The molar ratio of the starting materials be used in the reaction may be freely selected; however, it is favorable that the reaction is effected at the equimolar ratio or a ratio close thereto.
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
Production process M (for the present compounds wherein X is X1 and R6 is tert-butyl)
This is the production process in which isobutene (CH2=C(CH3)2) is reacted with a compound of formula (24).
The reaction is effected in the presence of an appropriate acid catalyst and in an inert solvent.
The solvent which can be used may include, for example, hydrocarbons such as toluene, benzene, and xylene; halogenated hydrocarbons such as dichloromethane, chloroform, 1,2-dichloroethane, and chlorobenzene; ethers such as 1,2-dimethoxyethane, tetrahydrofuran, and dioxane, dialkyl (e.g., C1-C4) ethers (e.g., diethyl ether, diisopropyl ether); and esters such as ethyl acetate. If necessary, these solvents may also be used in admixture.
The acid catalyst which can be used may include, for example, inorganic acids such as hydrochloric acid, hydrobromic acid, perchloric acid, sulfuric acid, nitric acid, and phosphoric acid; and organic acids such as trifluoroacetic acid, trichloroacetic acid, methanesulfonic acid, benzene-sulfonic acid, p-toluenesulfonic acid, and camphorsulfonic acid. In particular, sulfuric acid is preferably used.
The reaction temperature although it can be usuallv selected in the

range of -50°C to 50°C or the boiling point of a solvent used in the reaction, is usually in the range of 0°C to 30°C,
The molar ratio of the starting materials to be used in the reaction may be suitably selected; however, the reaction is preferably effected with the use of isobutene in an amount of 1 mole or more relative to 1 mole of the compound of formula (24).
After completion of the reaction, the reaction mixture is subjected to ordinary post-treatments such as extraction with an organic solvent and/or concentration. Thus, the desired present compounds can be isolated. If necessary, further purification may be carried out by an ordinary technique such as chromatography, distillation, or recrystallization.
For the present compounds, there may exist optical isomers based on the presence of at least one asymmetric carbon atom, and the optical isomers having biological activity, whether they are either in (+)-form or in (-)-form, and their mixtures at any ratio are, of course, included within the scope of the present invention. Furthermore, there may exist geometrical isomers based on the presence of at least one double bond, and the geometrical isomers having biological activity, whether they are either in cis-form or in trans-form, and their mixtures at any ratio are, of course, included within the scope of the present invention.
The compounds of formula (12), which are useful as the intermediates for the production of the present compounds, also have insecticidal/-acaricidal activity and can therefore be formulated or used as the active ingredients of insecticidal/acaricidal agents, in the same manner as the case of the present compounds.
The specific examples of the present compounds are shown below; however, the present compounds are not limited to these examples.

In the above formulae, (R1)a, R2, R3 and M2 are as defined in Table 1 below, and R6 is as defined in Tables 2 to 19 below.

The following will describe various processes for producing the intermediates in the production of the present compounds.
The compounds of formula (15) as the intermediates for the production of the present compounds can be produced, for example, according to the following schemes I to VI.

wherein all the variable are as defined above, with the proviso that R6 is not hydrogen.

wherein all the variable are as defined above, with the proviso that R6 is not hydrogen.

wherein TBDMSCl is tert-butyldimethylsillyl chloride, Z1 is oxygen or sulfur, and the other variables are as defined above, with the proviso that R6 is not hydrogen.

wherein all the variables are as defined above, with the proviso that R6 is not hydrogen.

The compounds of formula (18) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme VII.

The halide compounds of formula (16) and alcohol compounds of formula (17), both as the intermediates for the production of the present compounds, are commercially available or can be produced, for example, according to the publications: J. Org. Chem., 56, 1037-1041 (1991); Izvest. Akad. Nauk S.S.S.R., Otdel. Khim. Nauk, IQfiQ, 447-451 [CA (Chemical Abstracts) vol. 54, 22344d]; and Doklady Akad. Nauk S.S.S.R. 132, 606-608 (1960) [CA (Chemical Abstracts) vol. 54, 22331h], or according to the following scheme VIII.

The compounds of formula (19) or (20) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme IX or X.

A1-3,A1-4,A1-5, or A1-6,

The compounds of formula (22) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XI, XII, XIII, XIV, or XV.

wherein Y1 is oxygen or NH, R52 is a protecting group for the hydroxyl group of phenol or for the amino group of aniline, such as benzoyl, acetyl, or tert-butylmethylsillyl (TBDMS), and the other variables are as defined above.

wherein R53 is methyl or ethyl, R54 is a protecting group for the hydroxyl group of phenol, such as benzoyl or acetyl, and the other variables are as defined above.
Scheme XIII (in the case where X is X1 A1 is A1-2, A1-3, A1-4, A1-5, or A1-6, Q1 Y, and Z are all oxygen, and R7 is methyl)

wherein R53 is methyl or ethyl, R55 is a protecting group for the hydroxyl group of phenol, such as benzyl, DIBAL means diisobutylaluminum hydride, and the other variables are as defined above.

wherein R55 is a protecting group for the hydroxyl group of phenol, such as benzyl, R56 is acetyl or benzoyl, PCC means pyridinium chlorocromate, and the other variables are as defined above.

The compounds of formula (21) as the intermediateg for the production of the present compounds are commercially available or can be produced, for example, according to the following scheme XVI,

wherein L^ is a leaving group such as halogen, hydroxysulfonyloxy, or 2,4,6-trimethylbenzenesulfonyloxy, and the other variables are as defined above.
The compounds of formula (33), (34), (35), (36), or (37), as the intermediates for the production of the present compounds, are commercially available or can be produced by the methods widely known in the art or by the methods as described in the publications: [compounds of formula (33) wherein J is sulfur] J. Org. Chem,, 3Q, 1284 (1965); [compounds of formula (35) wherein J is oxygen] J. Am. Chem. Soc, 81, 714 (1959); [compounds of formula (35) wherein J is sulfurl Justus Liebies Ann. Chem., 590. 123 (1954).

The compounds of formula (19) or (20) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XVII.

The compounds of formula (39) can be produced, for example, according to the following schemes XVIII-1 to XVIII-9.

A11-8:-G2-(CR19R=20)j-(CR23=CR24)h-(CR225R26)=(CR27=CR28)p

wherein all the variables are as defined above.
Scheme XVIII-3 (in the case where A^ is A^-11)

The compounds of formula (25) as the intermediates for the production of the present compounds can be produced, for example, according to scheme XIV.

The compounds of formula (26) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XX,

The compounds of formula (21) as the intermediates for the produc-ion of the present compounds are commercially available or can be produced, for example, according to the following scheme XXL

The carbonyl compounds of formula (22) as the intermediates for the production of the present compounds can be produced, for example, according to the following schemes XXI-1 to XXII-5.

■
Scheme XXII-2 (in the case where X is X1 A1 is A1-8, and Y and Z are both oxygen)

Scheme XXII-3 (in the case where X is X1 R7 is hydrogen, W is W1 A1 is A1-8, G1 is G1-1, al is 0, and Y and Z are both oxygen)

V
wherein R105 is methyl or ethyl, W1 is a benzene ring or a heterocyclic ring containing no -NH- linkage in the ring thereof, and the other variables are as defined above.

Scheme XXII-4 (in the case where X is X1 R1 is hydrogen, W is W1 A1 is A^-8, G1 is G1-1, al is 0, and Y and Z are both oxygen)

wherein R108 is methyl or ethyl, or two R108 are combined together at their ends to form ethylene or trimethylene, and the other variables are as defined above.

Scheme XXII-5 (in the case where X is X1 R7 is hydrogen, A1 is A1-7, G^ is G1-1, al is 0, W is W\ t, h, u, and p are 0, j is 1, R29 and R30 are both hydrogen, and Y and Z are both oxygen)

The compounds of formula (24) as the intermediates for the produc-on of the present compounds can be produced, for example, according to the following scheme XXIII.

Some of the compounds of formula (41), (42), or (43) are commercially available or can be produced according to the following schemes XXIV-1 to XXIV-4.

wherein R106is methyl or ethyl, R107Ms C1-C6 alkyl, C3-C6 cycloalkyl, or phenyl or benzyl, each of which may be optionally substituted with C1-C4 alkyl or C1-C3 alkoxy, and the other variables are as defined above.

Scheme XXIV-3
.
wherein all the variables are as defined above.

wherein all the variables are as defined above. The starting compounds of formula (47)
wherein R109 and R110 are L1, Q4H, CHO, CH(0R108)2, CO2H, CO2R105 COCH3, or CH2L1 and the other variables are as defined above, which are used in the

lemes XXII-3, XXII-4, XXII-5, XXIV-1, XXIV-2, XXIV-3, and XXIV-4, and ler compounds are commercially available or can be produced, for example, the methods as described in the following publications. In the case where W1 is a pyridazine ring:
J. Heterocyclic Chem., 5, 845 (1968);
Monatschefte fur Chem., 110, 365 (1979), etc. In the case where W1 is a pyrimidine ring:
Justus Liebigs Ann. Chem., 684, 209 (1965);
J. Heterocyclic Chem., 28, 1281 (1991);
Chem. Ber., 97, 3407 (1964);
J. Chem. Soc, 1965, 5467;
Aust. J. Chem., 19, 2321 (1966), etc. In the case where W^ is a pyradine ring:
J. Org. Chem., 54, 640 (1089) etc. In the case where W1 is an oxazole ring:
J. Org Chem., 57, 4797 (1992) etc. In the case where W1 is an isoxazole ring:
Chem. Pharm. Bull, 14, 92 (1966);
Chem. Pharm. Bull, 14, 1277 (1966);
Chem. Pharm. Bull., 19, 46 (1971);
J. Chem. Res. Synop., 1994, 116;
V
Synthesis, 1976, 992, etc. In the case where W1 is a thiazole ring:
J.Am. Chem. Soc, 72, 5221 (1950) etc. In the case where W1 is an isothiazole ring:
J. Chem. Soc, 1959, 3061 etc. In the case where W1 is an imidazole ring:
Tetrahedron Lett, 26, 1915 (1985) etc.

In the case where W1 is a pyrazole ring: Chem. Ber., 112, 1712 (1979); Chem. Ber., 116, 1520 (1983); JP-A 63-185964/1988; Tetrahedron, 29, 441 (1973); J. Chem. Soc, Chem. Commun., 1969, 66; J Org. Chem., 35, 3451 (1970); Chem. Ber., 103, 2356 (1970), etc.
The compounds of formula (19) or (20) wherein X is X2, as the intermediates for the production of the present compounds, can be produced, for example, according to the following scheme XXV.

wherein L3 is halogen (e.g., chlorine, bromine, iodine), mesyloxy, or tosyloxy, R151 is a protecting group for alcohols, such as described in PROTECTIVE GROUPS IN ORGANIC SYNTHESIS, TW. Greene, RG.M. Wuts, A WILEY-INTERSCIENCE PUBLICATION, JOHN WILEY & SONS, INC., pp. 10-142; e.g., benzoyl, and the other variables are as defined above.
The compounds of formula (48) or (49) in the scheme XXV can be produced, for example, according to the following schemes XXVT to XXXXIII.

wherein L5 is halogen (e.g., chlorine, bromine, iodine), mesyloxy, or tosyloxy, Q8 is oxygen, sulfur, or NR33, R33 is hydrogen or C1-C3 alkyl, and the other variables are as defined above.

Scheme XXVIII (in the case where A2 is A2-3 and U3 is U3-2)

wherein all the variables are as defined above.

wherein Q9 is oxygen, sulfur, or NR34, R34 is hydrogen or C1-C3 alkyl, and the other variables are as defined above.

wherein R152 is a protecting group for alcohols (as described in PROTECTIVE GROUPS IN ORGANIC SYNTHESIS, TW. Greene, RG.M. Wuts, A WILEY-INTERSCIENCE PUBLICATION, JOHN WILEY & SONS, INC., pp. 10-142; as a protecting group selectively removable for R151 for example, when R151 is benzoyl, R152 is tetrahydropyranyl), and the other variables are as defined above.

wherein R153 is a protecting group (as described in PROTECTIVE GROUPS IN ORGANIC SYNTHESIS, T.W. Greene, RG.M. Wuts, A WILEY-INTERSCIENCE PUBLICATION, JOHN WILEY & SONS, INC., pp. 143-170 and 277-405; for example, when Q4 is oxygen, R153 is benzoyl), and the other variables are as defined above.

Scheme XXXIV (in the case where A2 is A2-5 and U3 is U3-2)

wherein all the variables are as defined above.

Scheme XXXV-1 (in the case where A2 is A2-5 and U3 is U3-3)

wherein L5 is halogen (e.g., chlorine, bromine, iodine), mesyloxy, or tosyloxy, and the other variables are as defined above.

Scheme XXXVIII (in the case where A2 is A2-7 and U3 is U3-2)

wherein all the variables are as defined above.

Scheme XXXIX-1 (in the case where A2 is A1-7 and U3 is U3-3)

wherein all the variables are as defined above.

Scheme XXXX (in the case where A2 is A2-8 and U3 is U3-2)

wherein all the variables are as defined above.

Scheme XXXXM (in the case where A' is A'-S and U' is U'-3)

wherein all the variables are as defined above.

The compounds of formula (27) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XXXXIV.

wherein all the variables are as defined above.

The compounds of formula (28) as the intermediates for the production of the present compounds can be produced, for example, according to the following schemes XXXXV to XXXXVIL

The compounds of formula (29) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XXXXVIII.

The compounds of formula (32) as the intermediates for the production of the present compounds can be produced, for example, according to the following scheme XXXXIX.

The harmful insects and harmful ticks and mites, against which the present compounds exhibit controlling activity, may include, for example, the following:
The present compounds are satisfactorily effective for the control of various noxious insects, mites and ticks, examples of which are as follows:
Hemiptera:
Delphacidae such as Laodelphax striatellus, Nilaparvata lugenSy and Sogatella furcifera, Deltocephalidae such as Nephotettix cincticeps and Empoasca onukh, Aphididae such as Aphis gossypii and Myzus persicae, Pentatomidae, Aleyrodidae such as Trialeurodes vaporariorum, Bemisia tabaci, and Bemisia argentifolii, Coccidae, Tingidae, Psyllidae, etc.
Lepidoptera:
Pyralidae such as Chilo suppressalis, Cnaphalocrocis medinalis, Ostrinia nubilalis, and Parapediasia teterrella, Noctuidae such as Spodoptera litura, Spodoptera exigua, Pseudaletia separata, Mamestra brassicae, Agrotis ipsilon, Ttichoplusia spp., HeJiothisspp., Helicoverpa spp. and Earias spp., Pieridae such as Pieris rapae crucivora, Tortricidae such as Adoxophyes orana fasciata, Grapholita molesta, and Cydia pomonella, Carposinidae such as Carposina niponensis, Lyonetiidae such as Lyonetia clerkella, Gracillariidae such as Phyllonorycter ringoniella, Phyllocnistidae such as Phyllocnistis citrella, Yponomeutidae such as Plutella xylostella, Gelechiidae such as Pectinophora gossypiella, Arctiidae, Tineidae, etc.
Biptera:
CaJicidae, Aedes spp,, Anopheles spp., Chironomidae, Muscidae, Calliphoridae, Sarcophagidae, Anthomyiidae, Cecidomyiidae, Agromyzidae, Tephritidae, Brosophilidae, Psychodidae, Simuliidae, Tabanidae, Stomoxyidae, etc.
Coleoptera:

Chrysomelidaey Scarabaeidae, Curculionidae, Attelabidae, Coccinellidae, Cerambycidae, Tenebrionidae, etc.
Thysanoptera:
Thnpidae such as Thrips spp., e.g., Thrips palmi, Frankliniella spp., e.g., Frankliniella occidentalism Sciltothrips spp., e.g., Sciltothrips dorsalis, and Phlaeotberipidae, etc.
Hymenoptera:
Tenthredinidae, Formicidae, Vespidae, etc.
Dictyoptera:
Blattidae, Blattellidae, etc.
Orthoptera:
Acrididae, Gryllotalpidae, etc,
Aphaniptera:
Purex irritans etc.
Anoplura:
Pediculus humanus capitis etc.
Isoptera:
Termitidae etc,
Acarina:
Tetranychidae such as Tetranychus spp. and Panonychus spp,, Tarsonemidae, Eriophyidae, Acaridae, Ixodidae, etc.
The present compounds are also effective for the control of various noxious insects, mites and ticks with resistance to conventional insecticides or acaricides.
When the present compounds are used as the active ingredients of insecticidal/acaricidal agents, they may be used as such without addition of any other ingredients. The present compounds are, however, usually mixed with solid carriers, liquid carriers, gaseous carriers, or baits, and if necessary,

with surfactants and other auxiliaries, and formulated into various forms, such as oil sprays, emulsifiable concentrates, wettable powders, flowables, granules, dusts, aerosols, fumigants (e.g., foggings), or poison baits.
Each of these formulations may usually contain at least one of the present compounds as an active ingredient in an amount of 0.01% to 95% by weight.
The solid carrier which can be used in the formulation may include, for example, fine powder or granules of clay materials such as kaolin clay, diatomaceous earth, synthetic hydrated silicon oxide, bentonite, Fubasami clay, and acid clay; various kinds of talc, ceramics, and other inorganic minerals such as sericite, quartz, sulfur, activated carbon, calcium carbonate, and hydrated silica; and chemical fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, urea, and ammonium chloride.
The liquid carrier may include, for example, water; alcohols such as methanol and ethanol; ketones such as acetone and methyl ethyl ketone; hydrocarbons such as hexane, cyclohexane, kerosene, and light oil; esters such as ethyl acetate and butyl acetate; nitriles such as acetonitrile and isobutyronitrile; ethers such as diisopropyl ether and dioxane; acid amides such as N,N-dimethylformamide and N,N-dimethylacetamide; halogenated hydrocarbons such as dichloromethane, trichloroethane, and carbon tetrachloride; dimethyl sulfoxide; and vegetable oils such as soybean oil and cottonseed oil.
The gaseous carrier or propellant may include, for example, Freon gas, butane gas, LPG (liquefied petroleum gas), dimethyl ether, and carbon dioxide.
The surfactant may include, for example, alkyl sulfates, alkyl sulfonates, alkyl arylsulfonates, alkyl aryl ethers and their polyoxyethylene derivatives, polyethylene glycol ethers, polyhydric alcohol esters, and sugar

alcohol derivatives.
The auxiliaries such as fixing agents or dispersing agents may include, for example, casein, gelatin, polysaccharides such as starch, gum arabic, cellulose derivatives, and alginic acid, lignin derivatives, bentonite, sugars, and synthetic water-soluble polymers such as polyvinyl alcohol, polyvinyl pyrrolidone, and polyacrylic acid.
The stabilizer may include, for example, PAP (isopropyl acid phosphate), BHT (2,6-di-tert-butyl-4-methylphenol), BHA (mixtures of 2-tert-butyl-4-methoxyphenol and 3-tert-butyl-4-methoxyphenol), vegetable oils, mineral oils, surfactants, fatty acids, and their esters.
The base material for used in poison baits may include, for example, bait materials such as grain powder, vegetable oils, sugars, and crystalline cellulose; antioxidants such as dibutylhydroxytoluene and nordihydro-guaiaretic acid; preservatives such as dehydroacetic acid; substances for preventing erroneous eating, such as red pepper powder; attractant flavors such as cheese flavor or onion flavor.
The formulations thus obtained are used as such or after diluted with water. Furthermore, they may be used in admixture with or separately but simultaneously with other insecticides, nematocides, acaricides, bactericides, fungicides, herbicides, plant growth regulators, synergists, fertilizers, soil conditioners and/or animal.
The insecticide, nematocide and/or acaricide which can be used may include, for example, organophosphorus compounds such as Fenitrothion [0,0-dimethyl 0-(3-methyl-4-nitrophenyl)phosphorothioate], Fenthion [0,0-dimethyl 0-(3-methyl-4-(methylthio)phenyl)phophorothioate], Diazinon [0,0-diethyl-0-2-isopropyl-6-methylpyrimidin-4-ylphosphorothioate], Chlor-pyriphos [0,0-diethyl-0-3,5,6-trichloro-2-pyridylphosphorothioate], Ace-phate [0,S-dimethylacetylphosphoramidothioate], Methidathion [S-2,3-di-

hydro-5-methoxy-2-oxo-l,3,4-thiadiazol-3-ylmethyl 0,0-dimethylphosphoro-dithioate], Disulfoton [0,0-diethyl S-2-ethylthioethylphosphorothioate], DDVP [2,2-dichlorovinyldimethylphosphate], Sulprofos [0-ethyl 0-4-(meth-ylthio)phenyl S-propyl phosphorodithioate], Cyanophos [0-4-cyanophenyl 0,0-dimethylphosphorothioate], Dioxabenzofos [2-methoxy-4H-l,3,2-benzo-dioxaphosphinine-2-sulfide], Dimethoate [0,0-dimethyl-S-(N-methylcar-bamoylmethyl)dithiophosphate], Phenthoate [ethyl 2-dimethoxyphosphino-thioylthio(phenyl)acetate], Malathion [diethyl(dimethoxyphosphinothioyl-thio)succinate], Trichlorfon [dimethyl 2,2,2-trichloro-l-hydroxyethylphos-phonate], Azinphos-methyl [S-3,4-dihydro-4-oxo-l,2,3-benzotriazin-3-yl-methyl 0,0-dimethylphosphorodithioate], Monocrotophos [dimethyl (E)-1-methyl-2-(methylcarbamoyl)vinylphosphate], Ethion [0,0,0',0'-tetraethyl S,S'-methylenebis(phosphorodithioate)], and Profenofos [0-4-bromo-2-chloro-phenyl 0-ethyl S-propyl phosphorothioate]; carbamate compounds such as BPMC (2-sec-butylphenylmethylcarbamate), Benfuracarb [ethyl N-[2,3-di-hydro-2,2-dimethylbenzofuran-7-yloxycarbonyl(methyl)aminothio]-N-isopro-pyl-p-alaninate], Propoxur [2-isopropoxyphenyl N-methylcarbamate], Car-bosulfan [2,3-dihydro-2,2-dimethyl-7-benzo[b]furanyl N-dibutylaminothio-N-methylcarbamate], Carbaril [1-naphthyl-N-methylcarbamate], Methomyl [S-methyl-N-[(methylcarbamoyl)oxy]thioacetimidate], Ethiofencarb [2-(eth-ylthiomethyl)phenylmethylcarbamate], Aldicarb [2-methyl-2-(methylthio)-propionaldehyde 0-methylcarbamoyloxime], Oxamyl [N,N-dimethyl-2-meth-ylcarbamoyloxyimino-2-(methylthio)acetamide], Fenothiocarb [S-4-phenoxy-butyl]-N,N-dimethylthiocarbamate], Thiodicarb [3,7,9,13-tetramethyl-5,11-dioxa-2,8,14-trithia-4,7,9,12-tetraazapentadeca-3,12-diene-6,10-dione], and Alanycarb [ethyl (Z)-N-benzyl-N-{[methyl(l-methylthioethylideneaminooxy-carbonyl)amino]thio}-p-alaninate]; pyrethroid compounds such as Etofen-prox [2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzylether], Fenvaler-

ate [(RS)αcyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutyr-ate], Esfenvalerate [(S)-α-cyano-3-phenoxybenzyl (S)-2-(4-chlorophenyl)-3-methylbutyrate], Fenpropathrin [(RS)αcyano-3'phenoxybenzyl 2,2,3,3-tetramethylcyclopropanecarboxylate], Cypermethrin [(RS)αcyano-3-phe-noxybenzyl (lRS,3RS)-3-(2,2-dichlorovinyl)-2,2-diinethylcyclopropanecarbox-ylate], Permethrin [3-phenoxybenzyl (IRS, 3RS)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate], Cyhalothrin [(RS)αcyano-3-phenoxy-benzyl (Z)-(lRS)-cis-3-(2-chloro-3,3,3-trifluoroprop-l-enyl)-2,2-dimethylcyclo-propanecarboxylate], Deltamethrin [(S)αcyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate], Cycloprothrin [(RS)αcyano-3-phenoxybenzyl (RS)-2,2-dichloro-l-(4-ethoxyphenyl)cyclo-propanecarboxylate], Fluvalinate (a-cyano-3-phenoxybenzyl N-(2-chloro-a,a,a-trifluoro-p-tolyl)-D-valinate), Bifenthrin (2-methylbiphenyl-3-yl-methyl) (Z)-(lRS)-cis-3-(2-chloro-3,3,3-trifluoroprop-l-enyl)-2,2-dimethyl-cyclopropanecarboxylate), Acrinathrin [(S)αcyano-(3-phenoxyphenyl)-methyl [lR-{la(S*),3α(Z)}]-2,2-dimethyl-3-[3-oxo-3-(2,2,2-trifluoro-l-(tri-fluoromethyl)ethoxy-l-propenyl)cyclopropanecarboxylate], 2-methyl-2-(4-bromodifluoromethoxyphenyl)propyl (3-phenoxybenzyl) ether, Traromethrin [(S)αcyano-3-phenoxylbenzyl(lR,3R)-3-[(rRS)(l,1,2',2'-tetrabromoethyl)]-2,2-dimethylcyclopropanecarboxylate], and Silafluofen [4-ethoxylphenyl [3-(4-fluoro-3-phenoxyphenyl)propyl]dimethylsilane]; thiadiazine derivatives such as Buprofezin (2-tert-butylimino-3-isopropyl-5-phenyl-l,3,5-thiadiazin-4-one; nitroimidazolidine derivatives such as Imidacloprid [l-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylidenamine]," Nereistoxin derivatives such as Cartap [S,S'-(2-dimethylaminotrimethylene)bis(thiocarbamate)], Thiocyclam [N,N-dimethyl-l,2,3-trithian-5-ylamine], and Bensultap [S,S'-2-dimethylaminotrimethylene di(benzenethiosulfonate)]; N-cyanoamidine derivatives such as acetamiprid [N-cyano-N'-methyl-N'-(6-chloro-3-pyridyl-

methyl)acetamidine]; chlorinated hydrocarbon compounds such as Endo-sulfan [6,7,8,9,10,10-hexachloro-l,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepinoxide], yBHC (1,2,3,4,5,6-hexachlorocyclohexane), and l,l-bis(chlorophenyl)-2,2,2-trichloroethanol; benzoylphenylurea compounds such as Chlorfluazuron [l-(3,5-dichloro-4-(3-chloro-5-trifluoromethylpyridin-2-yloxy)phenyl)-3-(2,6-difluorobenzoyl)urea], Teflubenzuron [l-(3,5-dichloro-2,4-difluorophenyl)-3-(2,6-difluorobenzoyl)urea], and Fulphenoxron [l-(4-(2-chloro-4-trifluoromethylphenoxy)-2-fluorophenyl)-3-(2,6-difluorobenzoyl)-urea]; formamidine derivatives such as Amitraz [N,N'-[(methylimino)-dimethylidine]-di-2,4-xylidine], and Chlordimeform [N'-(4-chloro-2-methyl-phenyl)-N,N-dimethylmethanimidamide]; thiourea derivatives such as Diafenthiuron [N-(2,6-diisopropyl-4-phenoxyphenyl)-N'-tert-butylcarbodi-imide]; Bromopropylate [isopropyl 4,4'-dibromobenzylate], Tetradifon [4-chlorophenyl 2,4,5-trichlorophenylsulfone], Quinomethionate [S,S-6-methylquinoxaline-2,3-diyldithiocarbonate], Propargate [2-(4-tert-butyl-phenoxy)cyclohexyl prop-2-yl sulfite], Fenbutatin oxide [bis[tris(2-methyl-2-phenylpropyl)tin]oxide], Hexythiazox [(4RS,5RS)-5-(4-chlorophenyl)-N-chlorohexyl-4-methyl-2-oxo-l,3-thiazolidine-3-carboxamide], Chlofentezine [3,6-bis(2-chlorophenyl)-l,2,4,5-tetrazine], Pyridaben [2-tert-butyl-5-(4-tert-butylbenzylthio)-4-chloropyridazin-3(2H)-one], Fenpyroximate [tert-butyl (E)-4-[(l,3-dimethyl-5-phenoxypyrazol-4-yl)methyleneaminooxymethyl]-benzoate], Tebfenpyrad [N-4-tert-butylbenzyl]-4-chloro-3-ethyl-l-methyl-5-pyrazolecarboxamide], polynactin complexes [e.g., tetranactin, dinactin, trinactin]; Milbemectin, Avermectin, Ivermectin, Azadilactin [AZAD], Pyrimidifen [5-chloro-N-[2-{4-(2-ethoxyethyl)-2,3-dimethylphenoxy}ethyl]-6-ethylpyrimidin-4-amine], Chlorfenapyr [4-bromo-2-(4-chlorophenyl)-l-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile], Tebfenozide [N-tert-butyl-N'-{4-ethylbenzoyl)-3,5-dimethylbenzohydrazide], and phenylpyrazole

derivatives.
When the present compounds are used as the active ingredients of insecticidal/acaricidal agents for agriculture, the application amount thereof is usually in the range of 0.1 to 100 g per 10 ares. When they are used after diluted with water in the case of emulsifiable concentrates, wettable powders, flowables, or similar formulations, the application concentration thereof is usually in the range of 1 to 10,000 ppm. In the case of granules, dusts, or similar formulations, they are applied as such formulations without any dilution. When the present compounds are used as the active ingredients of insecticidal/acaricidal agents for epidemic prevention, they are usually applied after diluted with water to a typical concentration of 0.1 to 500 ppm in the case of emulsifiable concentrates, wettable powders, flowable, or similar formulations; or they are applied as such in the case of oil sprays, aerosols, fumigants, poisonous baits, or similar formulations.
The application amount and concentration may vary depending upon the conditions including types of formulations, times, places and methods of application, kinds of noxious insects, mites and ticks, and degree of damage, and they can be increased or decreased without limitation to the above range.
Examples
The present invention will be further illustrated by the following production examples, formulation examples, and test examples; however, the present invention is not limited to these examples.
The following are production examples for the present compounds.
Production Example 1 Production of the present compound (2) by production process (E)
To a mixture of 0.37 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyloxyacetaldehyde and 10 ml of pyridine was added 0.20 g of

0-(3,3-dichloro-2-propenyl)hydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.39 g (yield, 74%) of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.0 1.5489.
Production Example 2 Production of the present compound (12) by production process F
First, 0.27 g of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde oxime, O.lOg of potassium carbonate, 0.16 g of benzyl bromide, and 10 ml of N,N-dimethylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.21 g (yield, 56%) of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde 0-benzyloxime, nD22.5 1.5402.
Production Example 3 Production of the present compound (16) by production process E
To a mixture of 0.37 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentanal and 10 ml of pyridine was added 0.13 g of 0-tert-butylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and

concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.22 g (yield, 50%) of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal 0-tert-butyloxime,
nD25.2 1.5275.
Production Example 4 Production of the present compound (30) by
production process E
To a mixture of 0.34 g of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenoxy)acetone and 10 ml of pyridine was added 0.11 g of O-ethylhydroxyl-amine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.32 g (yield, 81%) of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 0-ethyloxime, m.p., 65.4°C.
Production Example 5 Production of the present compound (14) by production process E
To a mixture of 0.42 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyloxyacetaldehyde and 10 ml of pyridine was added 0.13 g of 0-tert-butylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.45 g (yield, 92%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetalde-hyde 0-tert-butyloxime, nD25.2 1.5185.
Production Example 6 Production of the present compound (17) by

production process E
To a mixture of 0.37 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentanal and 10 ml of pyridine was added 0.20 g of 0-(3,3-di-chloro-2-propenyl)hydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.23 g (yield, 48%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal 0-(3,3-di-chloro-2-propenyl)oxime, nD25.2 1.5559.
Production Example 7 Production of the present compound (74) by production process C
First, 0.58 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol (which had been produced according to the method as disclosed in JP-A 8-337549/1996), 0.30 g of potassium carbonate, 0.43 g of chloroacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, and 10 ml of N,N-dimethylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography which afforded 0.74 g (yield, 82%) of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD22.3 1.5680.
Production Example 8 Production of the present compound (147) by production process E
To a mixture of 0.75 g of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-

oxy)phenoxy)butyloxyacetaldehyde and 10 ml of pyridine was added 0.15 g of hydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0,67 g (yield, 75%) of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde oxime, nD24.5 1.5278.
Production Example 9 Production of the present compound (152) by production process E
To a mixture of 5.58 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentanal and 50 ml of pyridine was added 1.25 g of hydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 2.44 g (yield, 41%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal oxime, nD23.4 1.5600,
Production Example 10 Production of the present compound (234) by production process E
To a mixture of 1,67 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyloxyacetone and 30 ml of pyridine was added 8.60 g of hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concen-

trated, which afforded 8.81 g (yield, 99%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone oxime, nD25.0 1.5460.
Production Example 11 Production of the present compound (104) by production process E
To a mixture of 0.43 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyloxyacetone and 10 ml of pyridine was added 0.15 g of 0-tert-butylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 0.45 g (yield, 90%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-tert-butyloxime, nD25.5 1.5170.
Production Example 12 Production of the present compound (177) by production process K
6
First, 0,45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.12 g of triethylamine, and 10 ml of tetra-hydrofuran were placed in a reaction vessel, to which 0.12 g of acetic anhydride was slowly added dropwise with stirring at room temperature. After completion of the addition, the reaction mixture was further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with saturated aqueous sodium hydrogencarbonate solution and water in this order, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.21 g (yield, 43%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-acetyloxime, nD25.6 1.5318.

Production Example 13 Production of the present compound (179) by production process K
First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.12 g of triethylamine, and 10 ml of tetra-hydrofuran were placed in a reaction vessel, to which 0.25 g of 4-trifluoro-methylbenzoyl chloride was slowly added dropwise with stirring at room temperature. After completion of the addition, the reaction mixture was further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.59 g (yield, 96%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-(4-trifluoromethylbenzoyl)oxime, nD25.6 1.5300.
Production Example 14 Production of the present compound (180) by production process K
First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime and 10 ml of tetrahydrofuran were placed in a reaction vessel, to which 0.12 g of tert-butylisocyannate was slowly added dropwise with stirring at room temperature. After completion of the addition, the reaction mixture was further stirred at room temperature for 30 minutes, poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.47 g (yield, 86%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetone 0-(N-tert-butylcarbamoyl)oxime, nD25.6 1.5191.
Production Example 15 Production of the present compound (216)

by production process K
First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.12 g of triethylamine, and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which a solution of 0.23 g of p-toluenesulfonyl chloride dissolved in 5 ml of tetrahydrofuran is slowly added dropwise with stirring under ice cooling. After completion of the addition, the reaction mixture is further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(p-toluenesulfonyl)oxime.
Production Example 16 Production of the present compound (217) by production process K
First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.12 g of triethylamine, and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which 0.16 g of N,N-diethyl-carbamoyl chloride is slowly added dropwise with stirring under ice cooling. After completion of the addition, the reaction mixture is further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel - chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyloxyacetone 0-(N,N-diethylcarbamoyl)oxime,
Production Example 17 Production of the present compound (218) by production process L

First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which 0.14 g of tert-butylisocyannate is slowly added dropwise with stirring at room temperature. After completion of the addition, the reaction mixture is further stirred at a temperature ranging from room temperature to 65°C, poured into water, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N-tert-butylthiocarbamoyl)oxime.
Production Example 18 Production of the present compound (213) by production process F
First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime and 10 ml of tert-butyl methyl ether are placed in a reaction vessel, to which 48 mg of 60% sodium hydride (in oil) is slowly added with stirring at room temperature in a stream of nitrogen gas. The mixture is stirred at room temperature until the evolution of hydrogen gas ceases, to which 0,11 g of chloroacetonitrile is added at room temperature, and the mixture is further stirred with heating under reflux. After completion of the reaction, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-cyanomethyloxime.
Production Example 19 Production of the present compound (214) by production process F

First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime and 10 ml of tert-butyl methyl ether are placed in a reaction vessel, to which 48 mg of 60% sodium hydride (in oil) is slowly added with stirring at room temperature in a stream of nitrogen gas. The mixture is stirred at room temperature until the evolution of hydrogen gas ceases, to which 0.29 g of tert-butyl bromoacetate is added at room temperature, and the mixture is further stirred with heating under reflux. After completion of the reaction, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-(tert-butoxycarbonyl-methyl)oxime.
Production Example 20 Production of the present compound (211) by production process A
First, 0.39 g of 5-(2,6-dichloro-4-hydroxyphnoxy)pentyloxyacetone 0-tert-butyloxime, 0.12 g of 1,1,3-tribromo-l-propene, 0.17 g of potassium carbonate, and 10 ml of N,N-dimethylformamide are placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dibromo-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-tert-butyloxime.
Production Example 21 Production of the present compound (207) by production process C

First, 0.46 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 0,25 g of potassium carbonate, 0.58 g of l-(5-(methanesulfonyloxy)pentyl-oxy)-2-butanone 0-tert-butyloxime, and 15 ml of N,N-dimethylformamide are placed in a reaction vessel. After stirring at 55°C to 60°C for 24 hours, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with ethyl acetate. The ethyl acetate layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 0.69 g (yield, 84%) of l-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)-2-butanone 0-tert-butyloxime,
ND23.4 1.5140.
Production Example 22 Production of the present compound (210) by production process D
To a mixture of 0.45 g of 2-(5-hydroxypentyloxy)cyclohexane 0-tert-butyloxime, 0.43 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 0.39 g of triphenylphosphine, and 15 ml of tetrahydrofuran is slowly added dropwise 0.30 g of diisopropyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen gas. After stirring at room temperature for 24 hours, the reaction mixture is concentrated to give a residue. This residue is subjected to silica gel chromatography, which affords 2-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)cyclohexanone 0-tert-butyloxime.
Production Example 23 Production of the present compound (103) by production process C
First, 0.55 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 0.30 g of potassium carbonate, 0.59 g of 4-(methanesulfonyloxy)butyloxy-acetone 0-tert-butyloxime, and 10 ml of N,N-dimethylformamide are placed in a reaction vessel. After stirring at 60°0 for 6 hours, the reaction mixture

is poured into diluted hydrochloric acid, and extracted twice with ethyl acetate. The ethyl acetate layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 0.71 g (yield, 77%) of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetone 0-tert-butyloxime, nD25.0 1.5170.
Production Example 24 Production of the present compound (203) by production process D
To a mixture of 0.51 g of 2-(2-hydroxyethoxy)ethoxyacetone 0-tert-butyloxime, 0,58 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 0.58 g of triphenylphosphine, and 20 ml of tetrahydrofuran is slowly added dropwise 0.49 g of diisopropyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen gas. After stirring at room temperature for 4 hours, the reaction mixture is concentrated to give a residue. This residue is subjected to silica gel chromatography, which affords 0.68 g (yield, 68%) of 2-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy)ethoxy-acetone 0-tert-butyloxime, nD23.0 1.5172.
Production Example 25 Production of the present compound (104) by production process M
First, 0.45 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxyacetone oxime, 0.3 ml of concentrated sulfuric acid, and 10 ml of toluene are placed in a reaction vessel, into which isobutene gas is blown with stirring under ice cooling, and the mixture is further stirred at room temperature. After completion of the reaction, the reaction mixture is slowly poured into a saturated aqueous sodium hydrogencarbonate solution, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to

silica gel chromatography, which affords 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-tert-butyloxime.
Production Example 26 Production of the present compound (185) by production process E
To a mixture of 1.29 g of 0-(2,4,6-trimethylbenzenesulfonyl)hydroxyl-amine (which had been produced according to the method as described in Synthesis, 1-17 (1977)) and 10 ml of diethyl ether was added 1.14 g of sodium l,l,l,3,3,3-hexafluoro-2-propyloxide with stirring under ice cooling, and the mixture was stirred for 2 hours. The suspended reaction mixture was filtered through Celite to give a filtrate which was a solution of 0-(l,l,l, 3,3,3-hexafluoro-2-propyl)hydroxylamine in diethyl ether. The addition of diethyl ether to this filtrate made the diethyl ether solution have the weight of 30 g. Then, 10 g of the diethyl ether solution and 0.1 ml of concentrated hydrochloric acid were poured into a reaction vessel containing 0,37 g of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal. After stirring at room temperature for 2 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to preparative thin layer chromatography, which afforded 0.27 g (yield, 50%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentanal 0-(l,l,l,3,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4850.
Production Example 27 Production of the present compound (186) by production process E
A mixture of 0.34 g of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenoxy)acetone, 0.24 g of 0-(3-(5-trifluoromethyl-2-pyridyloxy)propyl)-hydroxylamine, 0.14 g of pyridinium chloride, and 10 ml of pyridine was

stirred at room temperature for 2 hours. The reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 0.40 g (yield, 71%) of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-acetone 0-(3-(5-trifluoromethyl-2-pyridyloxy)propyl)oxime, nD23.0 1.5310.
Production Example 28 Production of compound (279) by production process D
To a mixture of 0.35 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenol, 0.32 g of 4-(hydroxy me thy l)benzaldehyde 0-(3,3-dichloro-2-prope-nyl)oxime, 0.32 g of triphenylphosphine, and 10 ml of dichloromethane was slowly added dropwise 0.25 g of diisopropyl azodicarboxylate. After stirring at room temperature for 12 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 0.43 g (yield, 67%) of 4-((2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)methyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 76.2°C.
Production Example 29 Production of compound (293) by production process E
To a mixture of 0.31 g of 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyloxy)acetophenone (which had been produced in Intermediate Production Example 2 as described below) and 10 ml of pyridine was added 0.07 g of 0-ethylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was

subjected to silica gel chromatography, which afforded 0.33 g (yield, 99%) of 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)aceto-phenone 0-ethyloxime, nD24.5 1.5948.
Production Example 30 Production of compound (303) by production process E
To a mixture of 0.21 g of 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyloxy)benzaldehyde and 10 ml of pyridine was added 0.09 g of 0-ethylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.21 g (yield, 92%) of 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzaldehyde 0-ethyloxime, m.p., 42.6°C.
Production Example 31 Production of compound (353) by production process E
To a mixture of 0,55 g of 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)ethyl)benzaldehyde (which had been produced in Intermediate Production Example 3 as described below) and 5 ml of pyridine was added 0.18 g of 0-propylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.45 g (yield, 72%) of 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde 0-propyloxime, m.p., nD24.5 1.5773.

Production Example 32 Production of compound (364) by production process E
To a mixture of 0.41 g of 5-acetyl-2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)pyridine and 10 ml of pyridine was added 0.17 g of 0-ethylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.40 g (yield, 89%) of 5-(l-(N-ethoxyimino)ethyl)-2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenoxy)propyloxy)pyridine, nD24.5 1.5701.
Production Example 33 Production of compound (369) by production process E
To a mixture of 0.43 g of 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyl)benzaldehyde and 5 ml of pyridine was added 0.15 g of 0-tert-butylhydroxylamine hydrochloride. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.38 g (yield, 75%) of 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)benzaldehyde 0-tert-butyloxime, nD25.5 1.5673.
Production Example 34 Production of compound (481) by production process D
To a mixture of 0.62 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenol, 0.54 g of 5-(hydroxymethyl)-2-furfural 0-(3,3-dichloro-2-propenyl)-

oxime, 0.57 g of triphenylphosphine, and 10 ml of dichloromethane was slowly added dropwise 0.44 g of diisopropyl azodicarboxylate with stirring under ice cooling. After stirring at room temperature for 12 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 0.43 g (yield, 69%) of
5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyl)-2-furfural 0-(3,3-dichloro-2-propenyl)oxime, m.p., 65.0°C.
Production Example 35 Production of compound (523) by production process I
To a mixture of 0.15 g of benzaldehyde and 10 ml of pyridine was added 0.56 g of 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.50 g (yield, 79.4%) of benzaldehyde 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)-oxime, nD22..5 1.5797.
Production Example 36 Production of compound (529) by production process I
To a mixture of 0.14 g of 4-(trifluoromethyl)benzaldehyde and 10 ml of pyridine was added 0.30 g of 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude

product was subjected to silica gel chromatography, which afforded 0,37 g (yield, 95.6%) of 4-(trifluoromethyl)benzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD21..0 1.5387.
Production Example 37 Production of compound (531) by production process I
To a mixture of 0.15 g of 4'-(trifluoromethyl)acetophenone and 10 ml of pyridine was added 0.30 g of 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.30 g (yield, 75.5%) of 4'-(trifluoromethyl)acetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD21..5 1,5420.
Production Example 38 Production of compound (545) by production process I
To a mixture of 0.07 g of trimethylacetaldehyde and 5 ml of pyridine was added 0,30 g of 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.31 g (yield, 96.8%) of trimethylacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyl)oxime, nD23..0 1.5178.
Production Example 39 Production of compound (564) by produc-

tion process I
To a mixture of 0.10 g of 4-methyl-2-pentanone and 5 ml of pyridine was added 0.40 g of 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)hydroxylamine hydrochloride. After stirring at room temperature for 1 hour, the reaction mixture was poured into5% aqueous citric acid solution, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0,42 g (yield, 95.4%) of 4-meth-yl-2-pentanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyl)oxime, nD24.5 1,5230.
Some specific examples of the present compounds are shown below with their compound numbers and physical properties, if any.
(1) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-ethyloxime, nD24.0 1.5310
(2) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(3,3-dichlorO-2-propenyl)oxime, nD24.0 1.5489
(3) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5661
(4) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(2-propenyl)oxime, nD23..5 1.5326
(5) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-benzyloxime, nD23..5 1.5471
(6) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-tert-butyloxime, nD23..5 1.5229
(7) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-methyloxime, nD23..5 1.5374
(8) (Z)-4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-

butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxiine, nD24.6 1.5498
(9) (E)-4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.6 1.5490
(10) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5213
(11) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-tert-butyloxime, nD24.5 1.4974
(12) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-benzyloxime, nD22.5 1.5402
(13) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(4-(trifluoromethyl)benzyl)oxime, nD22.5 1.5166
(14) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-tert-butyloxime, nD25.2 1.5185
(15) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD25.2 1.5450
(16) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-tert-butyloxime, nD25.2 1.5275
(17) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-(3,3-dichloro-2-propenyl)oxime, nD25.2 1,5559
(18) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-n-propyloxime, nD19.5 1.5373
(19) 5-(2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-(2-propenyl)oxime, nD19.5 1.5468
(20) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen tanal 0-(3,3-dibromo-2-propenyl)oxime, nD19.5 1.5742
(21) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-benzyloxime, nD23.7 1.5605
(22) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen

tanal 0-(4-methoxybenzyl)oxime, nD21.5 1.5587
(23) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal 0-(2,4-dinitrophenyl)oxime, m.p., 65.2°C
(24) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-(3,3-dichloro-2-propenyl)oxime, nD22.6 1.5602
(25) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-(3,3-dibromo-2-propenyl)oxime, nD22.6 1.5797
(26) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-tert-butyloxime, nD22.6 1.5309
(27) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-benzyloxime, nD22.6 1.5700
(28) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-ethyloxime, nD24.6 1.5427
(29) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tanal 0-methyloxime, nD22.6 1.5496
(30) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 0-ethyloxime, m.p., 65.4°C
(31) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 0-(3,3-dichloro-2-propenyl)oxime, nD23.2 1.5658
(32) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(33) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-
oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, HD^^^ 1.5513
(34) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD26.0 1.5390
(35) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(36) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-

oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(37) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(38) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(39) 2-(2-ethyl-6-inethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(40) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(41) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(42) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(43) 6-(2-ethyl-6-inethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(44) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(45) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(46) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(47) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime, nD25.5 1.5408
(48) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(49) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-acetone 0-(3,3-dichloro-2-propenyl)oxime
(50) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-

oxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(51) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(52) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(53) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(54) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(55) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetone 0-(3,3-dichloro-2-propenyl)oxiine
(56) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(57) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime
(58) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetone 0-(3,3-dichloro-2-propenyl)oxiine
(59) 3-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(60) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(61) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(62) 3-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(63) 3-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(64) 3-(2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-

ethoxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(65) 3-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(66) 3-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(67) 3-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(68) 3-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(69) 3-(2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)ethoxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(70) 3-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(71) 3-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(72) 3-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(73) 3-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyloxy)propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(74) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetal-dehyde 0-(3,3-dichloro-2-propenyl)oxime, nD22.3 1.5680
(75) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pionaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD22.3 1.5646
(76) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5509
(77) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-hyde 0-(3,3-dichloro-2-propenyl)oxime
(78) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone

0-(3,3-dichloro-2-propenyl)oxime
(79) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(80) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal 0-(3,3-dichloro-2-propenyl)oxiine
(81) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tanal O-(3,3-dichloro-2-propenyl)oxime
(82) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal 0-(3,3-dichloro-2-propenyl)oxime
(83) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(84) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-acetone 0-(3,3-dichloro-2-propenyl)oxime
(85) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propionaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(86) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butanal 0-(3,3-dichloro-2-propenyl)oxime
(87) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentanal 0-(3,3-dichloro-2-propenyl)oxime
(88) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexanal 0-(3,3-dichloro-2-propenyl)oxime
(89) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde 0-tert-butyloxime
(90) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetaldehyde 0-tert-butyloxime, nD25.6 1.5253
(91) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-tert-butyloxime, nD26.0 1.5181
(92) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-

acetaldehyde 0-tert-butyloxime
(93) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetaldehyde 0-tert-butyloxime
(94) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde O-tert-butyloxime
(95) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde O-tert-butyloxime
(96) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde O-tert-butyloxime
(97) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetaldehyde O-tert-butyloxime
(98) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde O-tert-butyloxime
(99) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetaldehyde O-tert-butyloxime
(100) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetaldehyde O-tert-butyloxime
(101) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone O-tert-butyloxime
(102) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone O-tert-butyloxime
(103) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone O-tert-butyloxime, nD25.0 1.5170
(104) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone O-tert-butyloxime, nD25.5 1.5170
(105) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone O-tert-butyloxime
(106) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-

acetone 0-tert-butyloxime
(107) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone 0-tert-butyloxime
(108) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-tert-butyloxime
(109) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-tert-butyloxime
(110) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone 0-tert-butyloxime
(111) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone 0-tert-butyloxime
(112) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetone 0-tert-butyloxime
(113) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetone 0-tert-butyloxime
(114) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetone 0-tert-butyloxime
(115) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetone 0-tert-butyloxime
(116) 3-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde 0-tert-butyloxime
(117) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)propionaldehyde 0-tert-butyloxime
(118) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)propionaldehyde 0-tert-butyloxime
(119) 3-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)propionaldehyde 0-tert-butyloxime
(120) 3-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-

hexyloxy)propionaldehyde 0-tert-butyloxime
(121) 3-(2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde O-tert-butyloxime
(122) 3-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propionaldehyde O-tert-butyloxime
(123) 3-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)propionaldehyde O-tert-butyloxime
(124) 3-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)propionaldehyde O-tert-butyloxime
(125) 3-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex-yloxy)propionaldehyde O-tert-butyloxime
(126) 3-(2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)ethoxy)propionaldehyde O-tert-butyloxime
(127) 3-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyloxy)propionaldehyde O-tert-butyloxime
(128) 3-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyloxy)propionaldehyde O-tert-butyloxime
(129) 3-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxy)propionaldehyde O-tert-butyloxime
(130) 3-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyloxy)propionaldehyde O-tert-butyloxime
(131) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-hyde O-tert-butyloxime
nD22.3 1.5371
(132) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone O-tert-butyloxime
(133) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pionaldehyde O-tert-butyloxime, nD2433 1.5345

(134) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-tert-butyloxime,nD24.5 1.5237
(135) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-
hyde 0-tert-butyloxime
(136) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone
O-tert-butyloxime
(137) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-
pionaldehyde 0-tert-butyloxime
(138) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal
0-tert-butyloxime
(139) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-
nal O-tert-butyloxime
(140) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal
0-tert-butyloxime
(141) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
acetaldehyde 0-tert-butyloxime
(142) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
acetone 0-tert-butyloxime
(143) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
' propionaldehyde 0-tert-butyloxime
(144) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
butanal 0-tert-butyloxime
(145) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
pentanal 0-tert-butyloxime
(146) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
hexanal 0-tert-butyloxime
(147) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-
oxyacetaldehyde oxime, nD24.5 1.5278

(148) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde oxime, m.p., 62.8°C
(149) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde oxime, nD21.2 1.5465
(150) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)aceto-phenone 0-(3,3-dichloro-2-propenyl)oxime, nD23.4 1.5929
(151) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)aceto-phenone 0-tert-butyloxime, nD23.4 1.5622
(152) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal oxime, nD23.4 1.5600
(153) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-isopropyloxime, nD23.0 1.5242
(154) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxycetaldehyde 0-sec-butyloxime, nD24.0 1.5211
(155) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-isobutyloxime, nD25.2 1.5206
(156) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-neopentyloxime, nD25.2 1.5106
(157) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(4-trifluoromethylbenzyl)oxime, nD24.8 1.5345
(158) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-methyloxime, nD24.7 1.5343
(159) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-ethyloxime, nD24.7 1.5291
(160) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-benzyloxime, nD24.7 1.5550
(161) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime, nD24.4h 1.5423

(162) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-phenyloxime, nD24.4 1.5613
(163) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-cyclohexyloxime, nD24.4 1.5289
(164) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(2,2,2-tribromoethyl)oxime, nD25.3 1.5671
(165) 5-(2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde 0-(2,2,2-trifluoroethyl)oxime, nD25.3 1.5058
(166) 4-(2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-isopropyloxime, nD25.3 1.5266
(167) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-isopropyloxime, nD25.3 1.5212
(168) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime, nD25.3 1.5445
(169) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime, nD25.3 1.5372
(170) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-isopropyloxime, nD25.3 1.5337
(171) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(2,2,2-trichloroethyl)oxime, nD25.3 1.5520
(172) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-phenyloxime, nD25.3 1.5725
(173) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-isopropyloxime, nD25.5 1.5208
(174) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(2,2,2-trichloroethyl)oxime, nD25.5 1.5378
(175) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-benzyloxime, nD25.5 1.5510

(176) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-ethyloxime, nD25.5 1.5262
(177) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-acetyloxime, nD25.6 1.5318
(178) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-pivaloyloxime, nD25.6 1.5195
(179) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(4-trifluoromethylbenzoyl)oxime, nD25.6 1.5300
(180) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N-tert-butylcarbamoyl)oxime, nD25.6 1,5191
(181) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N-phenylcarbamoyl)oxime, nD25.6 1.5546
(182) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde 0-(l,l,l,3,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4829
(183) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-bxyacetaldehyde 0-(l,l,l53,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4821
(184) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(l,l,l,3,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4807
(185) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(l,l,l,3,3,3-hexafluoro-2-propyl)oxime, nD24.5 1.4850
(186) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone 0-(3-(5-trifluoromethyl-2-pyridyloxy)propyl)oxime, nD23.0 1.5310
(187) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-nal 0-isopropyloxime
(188) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-isopropyloxime
(189) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-nal 0-(2,2,2-trichloroethyl)oxime

(190) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-nal 0-(2,2,2-trichloroethyl)oxime
(191) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-isopropyloxime
(192) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone 0-(2,2,2-trichloroethyl)oxime
(193) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-isobutyloxime
(194) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-isobutyloxime
(195) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-sec-butyloxime
(196) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-sec-butyloxime
(197) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(2,2,2-tribromoethyl)oxime
(198) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(2,2,2-tribromoethyl)oxime
(199) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-nal 0-(2,2,2-trifluoroethyl)oxime
(200) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(2,2,2-trifluoroethyl)oxime
(201) 4-(2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)-2-bu-tenyloxyacetone 0-tert-butyloxime
(202) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-2-bu-tynyloxyacetone 0-tert-butyloxime
(203) 2-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)ethoxyacetone 0-tert-butyloxime, nD23.0 1.5172

(204) 2-(N-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethyl)-N-methylamino)ethoxyacetone 0-tert-butyloxime
(205) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)cyclo-hexyloxyacetone 0-tert-butyloxime
(206) 7-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)heptyl-oxyacetone 0-tert-butyloxime
(207) l-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)-2-butanone 0-tert-butyloxime, HD^^^ 1.5140
(208) l-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)-3,3-dimethyl-2-butanone 0-tert-butyloxime, IID^^^ 1.5102
(209) 2-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)acetophenone 0-tert-butyloxime, nD23.4 1.5483
(210) 2-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)cyclohexanone 0-tert-butyloxime
(211) 5-(2,6-dichloro-4-(3,3-dibromo-2-propenyloxy)phenoxy)pen-tyloxyacetone 0-tert-butyloxime
(212) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-triphenylmethyloxime
(213) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-cyanomethyloxime
(214) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(tert-butoxycarbonylmethyl)oxime
(215) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(2,2-diethoxyethyl)oxime
(216) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(p-toluenesulfonyl)oxime
(217) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N,N-diethylcarbamoyl)oxime

(218) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone 0-(N-tert-butylthiocarbamoyl)oxime
(219) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde oxime
(220) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetaldehyde oxime
(221) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde oxime
(222) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-acetaldehyde oxime
(223) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetaldehyde oxime
(224) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetaldehyde oxime
(225) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetaldehyde oxime
(226) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde oxime
(227) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
propyloxyacetaldehyde oxime
(228) 4-(2-ethyI-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde oxime
(229) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetaldehyde oxime
(230) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetaldehyde oxime
(231) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
ethoxyacetone oxime

(232) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone oxime
(233) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone oxime
(234) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxy ace tone oxime, nD25.0 1.5460
(235) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone oxime
(236) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-acetone oxime
(237) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-oxyacetone oxime
(238) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetone oxime
(239) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-oxyacetone oxime
(240) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-oxyacetone oxime
(241) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone oxime
(242) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetone oxime
(243) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetone oxime
(244) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
pentyloxyacetone oxime
(245) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
hexyloxyacetone oxime

(246) 3-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde oxime
(247) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)propionaldehyde oxime
(248) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)propionaldehyde oxime
(249) 3-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)propionaldehyde oxime
(250) 3-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxy)propionaldehydeoxime
(251) 3-(2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)propionaldehyde oxime
(252) 3-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propionaldehyde oxime
(253) 3-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)propionaldehyde oxime
(254) 3-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)propionaldehyde oxime
(255) 3-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex-yloxy)propionaldehyde oxime
(256) 3-(2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)ethoxy)propionaldehyde oxime
(257) 3-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyloxy)propionaldehyde oxime
(258) 3-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyloxy)propionaldehyde oxime
(259) 3-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyloxy)propionaldehyde oxime

(260) 3-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyloxy)propionaldehyde oxime
(261) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-hyde oxime
(262) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone
oxime
(263) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-
pionaldehyde oxime
(264) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-
nal oxime
(265) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-
nal oxime
(266) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-
hyde oxime
(267) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone
oxime
(268) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-
pionaldehyde oxime
(269) 4-(2,6-diethyl-4-(3,3-dichlorO-2-propenyloxy)phenoxy)butanal
oxime
(270) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-
nal oxime
(271) 6-(2,6-diethyl-4-(3,3-dichlorO-2-propenyloxy)phenoxy)hexanal
oxime
(272) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
acetaldehyde oxime
(273) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
acetone oxime

(274) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propionaldehyde oxime
(275) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butanal oxime
(276) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentanal oxime
(277) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexanal oxime
(278) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)aceto-phenone oxime
(279) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 76.2°C
(280) 4-(2,6-dichloro-4-(3,3-dibromo-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 88.2°C
(281) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 88.0°C
(282) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-(3,3-dibromo-2-propenyl)oxime, m.p., 90.8°C
(283) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-
^ pyloxy)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5872
(284) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5852
(285) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5819
(286) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5941
(287) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-ethyloxime, nD21.5 1.5760

(288) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-ethyloxime, nD21.5 1.5664
(289) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-ethyloxime, nD21.5 1,5613
(290) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-tert-butyloxime, nD21.5 1.5628
(291) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-tert-butyloxime, nD21.5 1.5588
(292) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-tert-butyloxime, nD21.5 1.5528
(293) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-ethyloxime, nD24.5 1.5948
(294) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-tert-butyloxime, nD24.5 1.5949
(295) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5950
(296) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5943
(297) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-ethyloxime, m.p., 41.9°C
(298) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-tert-butyloxime, m.p., 56.4° C
(299) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-(3,3-dichloro-2-propenyl)oxime, nD24.5 1.5785
(300) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-(3,3-dibromo-2-propenyl)oxime, nD24.5 1.5909
(301) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-methyloxime, nD24.5 1.5802

(302) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde O-methyloxime nD24.5 1.5756
(303) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-ethyloxime, m.p., 42.6°C
(304) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-ethyloxime nD24.5 1.5723
(305) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde O-methyloxime, nD24.5 1.5871
(306) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde O-methyloxime, m.p,, 63.5°C
(307) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone O-methyloxime, nD25.5 1.5642
(308) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-propyloxime, nD22.5 1.5733
(309) 4'-(4-(2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone O-methyloxime, nD22.5 1.5686
(310) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)acetophenone 0-propyloxime, nD22.5 1.5589
(311) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde O-methyloxime, m.p., 95.9°C
(312) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-(2-propenyl)oxime, m.p., 75.6°C
(313) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-benzyloxime, m.p., 70.3°C
(314) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-tert-butyloxime, nD24.5 1.5713
(315) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde 0-iso-propyloxime, nD24.5 1.5643

(316) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde O-isobutyloxime, nD24.5 1.5571
(317) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzophenone 0-ethyloxime, nD24.5 1.5943
(318) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propiophenone O-ethyloxime, m.p., 42.4°C
(319) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)valerophenone O-ethyloxime, nD24.5 1.5535
(320) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde O-ethyloxime, nD24.5 1.5730
(321) 4'-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)acetophenone O-ethyloxime, m.p., 56.1°C
(322) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yloxy)acetophenone O-ethyloxime, nD24.5 1.5840
(323) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD24.01.6006
(324) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-benzyloxime, nD22.5 1.6095
(325) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-tert-butyloxime, nD23.0 1.5753
(326) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde O-ethyloxime, m.p., 84.8°C
(327) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-propyloxime, m.p., 45.4°C
(328) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-isopropyloxime, nD24.0 1.5858
(329) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-sec-butyloxime, m.p., 59.6°C

(330) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-allyl oxime, m.p., 63.9°C
(331) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)benzaldehyde 0-sec-butyloxime, nD24.5 1,5783
(332) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propiophenone oxime, m.p., 140.0°C
(333) 4-(5-(2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde oxime, m.p,, 90,1°C
(334) 4'-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxy)acetophenone oxime, m.p., 79.5°C
(335) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde oxime, nD24.0 1.5640
(336) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)valerophenone oxime, m.p., 87.0°C
(337) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)acetophenone oxime, m.p., 121.0°C
(338) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-propyloxime, IID^^^ 1.5703
(339) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-isopropyloxime, nD24.5 1.5653
(340) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-sec-butyloxime, nD24.5 1.5665
(341) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-iso-butyloxime, nD24.5 1.5579
(342) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-allyloxime, nD24.5 1.5990
(343) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-benzyloxime, nD24.5 1.5886

(344) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-(3,3-dichloro-2-propenyl)oxime, nD25.0 1.5965
(345) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-methyloxime, nD26.5 1.5947
(346) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-
yl)acetophenone 0-propyloxime, nD26.0 1.5808
(347) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-
yl)acetophenone O-propyloxime, nD26.0 1.5904
(348) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-tert-butyloxime, nD25.5 1.5717
(349) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-ethyloxime, nD26.0 1.5865
(350) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-yl)acetophenone 0-benzyloxime, nD25.5 1.6655
(351) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde O-methyloxime, nD24.5 1,5921
(352) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-ethyloxime, nD24.5 1.5846
(353) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde O-propyloxime, nD24.5 1.5773
(354) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-iso-propyloxime, nD24.5 1,5762
(355) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-sec-butyloxime, nD25.0 1.5718
(356) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-tert-butyloxime, nD26.0 1,5669
(357) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-allyl oxime, nD26.0 1.5849

(358) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phonoxy)eth-yl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD26.5 1.5932
(359) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)ph yl)benzaldehyde 0-benzyloxime, nD27.0 1.5967
(360) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)ph( noxy methyl)phenoxy)acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, m.p., 87!) C
(361) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phen(oxy)( th-yl)benzaldehyde 0-(4-tert-butylbenzyl)oxime, nD26.0 1.5818
(362) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)(th-yl)benzaldehyde 0-cyclohexyloxime, nD26.0 1.5685
(363) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)benzaldehyde 0-(3-phenylpropyl)oxime, nD26.0 1.5902
(364) 5-(l-(N.ethoxyimino)ethyl)-2-(3-(2,6-dichloro-4-(3,3-(li(:hl()r()-2-propenyloxy)phenoxy)propyloxy)pyridine, nD24.5 1.5701
(365) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)pr()-pyl)benzaldehyde 0-methyloxime, nD25.5 1.5876
(366) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)pro)-pyl)benzaldehyde 0-ethyloxime, nD26.0 1.5802
(367) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phcn()xy)pr()-pyl)benzaldehyde 0-propyloxime, nD25.5 1.5763
(368) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phoni)xy)pro-pyl)benzaldehyde 0-iso-propyloxime, nD25.5 1.5734
(369) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)ph(n()xy)pr()-pyl)benzaldehyde 0-tert-butyloxime, nD25.5 1.5673
(370) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)pr()-
pyl)benzaldehyde 0-allyl oxime, nD25.5 1.5844
(371) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phon()xy)pr()-
pyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD25.0- 1.5920

(372) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)acetophenone 0-iso-propyloxime
(373) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)acetophenone 0-butyloxime
(374) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-
yl)acetophenone 0-iso-butyloxime
(375) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)acetophenone 0-sec-butyloxime
(376) 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-
yl)benzaldehyde O-butyloxime
(377) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-
yl)benzaldehyde O-methyloxime
(378) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-
yl)benzaldehyde 0-ethyloxime
(379) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)benzaldehyde 0-propyloxime
(380) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)benzaldehyde 0-iso-propyloxime
(381) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)benzaldehyde 0-iso-butyloxime
(382) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)benzaldehyde 0-iso-butyloxime
(383) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)prO-pyl)benzaldehyde 0-sec-butyloxime
(384) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(385) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde O-methyloxime

(386) 4-(4-(2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyl)benzaldehyde 0-ethyloxime
(387) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyl)benzaldehyde 0-propyloxime
(388) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyl)benzaldehyde 0-iso-propyloxime
(389) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyl)benzaldehyde 0-butyloxime
(390) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-iso-butyloxime
(391) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bU-tyl)benzaldehyde 0-sec-butyloxime
(392) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-tert-butyloxime
(393) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone 0-(3,3-dichloro-2-propenyl)oxiine
(394) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone 0-methyloxime
(395) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ineth-yl)-2,2,2-trifluoroacetophenone 0-ethyloxime
(396) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone 0-propyloxime
(397) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone 0-iso-propyloxime
(398) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth yl)-2,2,2-trifluoroacetophenone 0-butyloxime
(399) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth yl)-2,2,2-trifluoroacetophenone 0-iso-butyloxime

(400) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-l)-2,2,2-trifluoroacetophenone O-sec-butyloxiiiie
(401) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone O-tert-butyloxiine
(402) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone O-(3,3-dichloro-2-propenyl)oxime
(403) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone O-methyloxime
(404) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-ethyloxime
(405) 4'-(2-(2,6-dichloro-4-(3,3-dicliloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-propyloxime
(406) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-iso-propyloxime
(407) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-butyloxime
(408) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-iso-butyloxime
(409) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-sec-butyloxime
(410) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone 0-tert-butyloxime
(411) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-(3,3-dichloro-2-propenyl)oxime
(412) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro pyl)-2,2,2-trifluoroacetophenone 0-methyloxime
(413) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro pyl)-2,2,2-trifluoroacetophenone O-ethyloxime

(414) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-propyloxime
(415) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-iso-propyloxime
(416) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-butyloxime
(417) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-iso-butyloxime
(418) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone 0-sec-butyloxime
(419) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone O-tert-butyloxime
(420) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-methyloxime
(421) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-propyloxime
(422) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-iso-propyloxime
(423) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-butyloxime
(424) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-iso-butyloxime
(425) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)benzaldehyde 0-sec-butyloxime
(426) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde 0-butyloxime
(427) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu tyloxy)benzaldehyde 0-propyloxime

(428) 4-(4-(2,6-dichloro-4-(3,3-dichloro-3-propenyloxy)phenoxy)bu tyloxy)benzaldehyde O-sec-butyloxime
(429) 4-(4-(2,6-dichloro-4-(3,3-dichloro-4-propenyloxy)phenoxy)bu tyloxy)benzaldehyde 0-butyloxime
(430) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-methyloxime
(431) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen tyloxy)benzaldehyde 0-propyloxime
(432) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-iso-propyloxime
(433) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-butyloxime
(434) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-iso-butyloxime
(435) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen' tyloxy)benzaldehyde O-sec-butyloxime
(436) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde 0-tert-butyloxime
(437) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde 0-methyloxime
(438) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde 0-ethyloxime
(439) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde 0-propyloxime
(440) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde 0-iso-propyloxime
(441) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-butyloxime

(442) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-iso-butyloxime
(443) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-sec-butyloxime
(444) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-tert-butyloxime
(445) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy) propyloxy)-5-pyridyl)acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(446) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde O-methyloxime
(447) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-ethyloxime
(448) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde O-propyloxime
(449) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-iso-propyloxime
(450) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-butyloxime
(451) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-iso-butyloxime
(452) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-sec-butyloxime
(453) (2-(4-(2,6'dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-tert-butyloxime
(454) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(455) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone O-methyloxime

(456) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-ethyloxime
(457) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-propyloxime
(458) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-iso-propyloxime
(459) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-butyloxime
(460) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-iso-butyloxime
(461) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-sec-butyloxime
(462) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-tert-butyloxime
(463) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone 0-(3,3-dichloro-2-propenyl)oxime
(464) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-methyloxime
(465) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyloxy)-5-pyridyl phenyl ketone 0-ethyloxime
■^
(466) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-propyloxime
(467) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-iso-propyloxime
(468) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-butyloxime
(469) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-iso-butyloxime

(470) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-sec-butyloxime
(471) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-tert-butyloxime
(472) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)-5-pyridyl phenyl ketone 0-(3,3-dichloro-2-propenyl)oxime
(473) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-methyloxime
(474) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-ethyloxime
(475) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-propyloxime
(476) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-iso-propyloxime
(477) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-butyloxime
(478) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-iso-butyloxime
(479) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-sec-butyloxime
(480) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-tert-butyloxime
(481) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural 0-(3,3-dichloro-2-propenyl)oxime, m.p., GS.O'^C
(482) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-methyloxime
(483) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-ethyloxime

(484) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde O-propyloxime
(485) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde O-iso-propyloxiine
(486) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ineth-yl)-2-thiophenecarboxaldehyde 0-butyloxime
(487) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-iso-butyloxime
(488) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-sec-butyloxime
(489) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-thiophenecarboxaldehyde 0-tert-butyloxime
(490) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)nieth-yl)-2-thiophenecarboxaldehyde 0-(3,3-dichloro-2-propenyl)oxime
(491) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde O-methyloxime
(492) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-ethyloxime
(493) 5-((2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-propyloxime
(494) 5-((2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-iso-propyloxime
(495) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-butyloxime
(496) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-iso-butyloxime
(497) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-sec-butyloxime

(498) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde 0-tert-butyloxime
(499) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-pyrrolcarboxaldehyde O-(3,3-dichloro-2-propenyl)oxinie
(500) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2-furfural O-(3,3-dibroino-2-propenyl)oxime
(501) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-methyloxime, nD26.0 1.5816
(502) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-ethyloxime, nD26.0 1.5772
(503) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-propyloxime, nD28.0 1.5732
(504) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-tert-butyloxime, nD27.5 1,5559
(505) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-allyloxime, nD25.5 1.5828
(506) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)acetophenone 0-(3,3-dichloro-2-propenyl)oxime, nD25.0 1.5906
(507) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-methyloxime, nnD26.5 1.5802
(508) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-ethyloxime, nD25.5 1.5744
(509) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-propyloxime, nD26.5 1.5708
(510) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-tert-butyloxime, nD26.5 1.5624
(511) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-allyloxime, nD26.5 1.5794

(512) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD26.5 1.5856
(513) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-methyloxime, nD25.5 1.5786
(514) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-ethyloxime, nD26.5 1.5717
(515) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-propyloxime, nD25.5 1.5692
(516) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-isopropyloxime, nD25.5 1.5656
(517) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-sec-butyloxime, nD26.5 1.5606
(518) 3'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone O-tert-butyloxime, nD25.5 1.5580
(519) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-2,2,2-trifluoroacetophenone oxime
(520) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-2,2,2-trifluoroacetophenone O-ethyloxime
(521) 4'-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxy)acetophenone O-ethyloxime
(522) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone 0-(l,l,l,3,3,3-hexafluoroisopropyl)oxime
(523) benzaldehydeO-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl. oxy)phenoxy)propyl)oxime, nD22.5 1.5797
(524) 4-(trifluoromethyl)benzaldehyde O-(3-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)propyl)oxime, nD22.5 1.5462
(525) acetaldehyde 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl oxy)phenoxy)propyl)oxime nD22.5 1.5437

(526) butanal O-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyl)oxime, nD22.5 1.5361
(527) trimethylacetaldehyde 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime,nD22.5 1.5262
(528) 4'-(trifluoromethyl)acetophenone O'(3-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)propyl)oxime, nD21.0 1.5433
(529) 4-(trifluoromethyl)benzaldehyde O-(4.(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime, nD21.0 1.5387
(530) trimethylacetaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxmne, nD21.5 1.5280
(531) 4'-(trifluoromethyl)acetophenone O-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime, nD21.5 1,5420
(532) acetaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime, nD21.5 1.5423
(533) benzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime, nD21.5 1.5731
(534) butanal O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyl)oxime, nD21.5 1.5332
(535) 4-chlorobenzaldehyde 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime, nD21.5 1.5850
(536) 4-chlorobenzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD21.5 1.5740
(537) 4-(trifluoromethyl)benzaldehyde O-(5-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime, nD20.5 1.5455
(538) 4'-(trifluoromethyl)acetophenone 0-(5-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime, nD20.5 1.5421
(539) benzaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime, nnD20.5 1.5756

(540) 4-chlorobenzaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2 propenyloxy)phenoxy)pentyl)oxime, nD20.5 1.5766
(541) acetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl oxy)phenoxy)pentyl)oxime, nD22.5 1.5391
(542) butanal O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe noxy)pentyl)oxime, nD22.5 1.5319
(543) hexanal O-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe noxy)propyl)oxime, nD22.5 1.5313
(544) hexanal O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyl)oxime, nD22.5 1.5288
(545) trimethylacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2 propenyloxy)phenoxy)pentyl)oxime, nD23.0 1,5178
(546) hexanal 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy) phenoxy)pentyl)oxime, nD23.0 1.5250
(547) 4'-(trifluoromethyl)acetophenone 0-(6-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)hexyl)oxime, nD20.5 1.5391
(548) 4-(trifluoromethyl)benzaldehyde O-(6-(2,6-dichloro-4-(3,3-di chloro-2-propenyloxy)phenoxy)hexyl)oxime, nD20.5 1.5412
(549) 4'-(trifluoromethyl)acetophenone O-(2-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)ethyl)oxime, nD23.5 1.5468
(550) 4-(trifluoromethyl)benzaldehyde O-(2-(2,6-dichloro-4-(3,3-di chloro-2-propenyloxy)phenoxy)ethyl)oxime, m.p., 79.8°C
(551) hexanal 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe noxy)hexyl)oxime, nD21.0 1.5238
(552) nonanal O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe noxy)pentyl)oxime, nD22.0 1.5189
(553) dodecylaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propen-yloxy)phenoxy)pentyl)oxime, nD22.0 1.5110

(554) nonanal 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyl)oxime, nD22.0 1.5166
(555) dodecylaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propen-yloxy)phenoxy)butyl)oxime, nD22.0 1,5100
(556) hexanalO-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-
noxy)ethyl)oxime, nD21.5 1.5351
(557) butanal O-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-
noxy)ethyl)oxime, nD21.5 1,5410
(558) butanal O-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyl)oxime, nD23.0 1.5295
(559) 3,3-dimethyl-2-butanone O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD24.5 1.5233
(560) acetone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)oxime, nD24.5 1,5350
(561) 2-ethylbutanalO-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime, nD24.5 1.5235
(562) 3,3-dimethyl-2-butanone O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD22.0 1.5277
(563) 4-methyl-2-pentanone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD24.5 1.5265
(564) 4-methyl-2-pentanone 0-(5-(2,6-dichloro.4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD24.5 1.5230
(565) n-butyloxyacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD25.5 1.5240
(566) cyclohexanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl oxy)phenoxy)pentyl)oxime, nD25.5 1.5440
(567) chloroacetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime, nD25.0 1.5451

(568) 6-chloro-3-pyridyl methyl ketone 0-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime, m.p., 79.5°C
(569) 6-chloro-3-pyridyl methyl ketone 0-(5-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime, m.p,, 67.7°C
(570) cyclohexanone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl' oxy)phenoxy)butyl)oxime, nD24.5 1.5470
(571) tetrahydrothiopyran-4-one 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD24.5 1.5650
(572) tetrahydrothiopyran-4-one 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD24.0 1.5612
(573) tetrahydro-4H-pyran-4-one O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime nD24.0 1.5459
(574) tetrahydro-4H-pyran-4-One 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD24.0 1.5440
(575) tetrahydrothiopyran-4-one 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD24.0 1.5541
(576) tetrahydro-4H-pyran-4-one O-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD24.0 1.5383
(577) 4-isopropylbenzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD24.0 1.5665
(578) 4-nitrobenzaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime, m.p., 76.4°C
(579) 4-isopropoxybenzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD24.0 1.5701
(580) 3-methyl-2-butanone O-(3-(2,6-dichloro-4-(3,3-dichloro-2.pro penyloxy)phenoxy)propyl)oxime, nD24.0 1.5330
(581) 3-methyl-2-butanone O-(4-(2,6-dichlorO-4-(3,3-dichloro-2-prO-penyloxy)phenoxy)butyl)oxime, nD24.0 1.5302

(582) 3-methyl-2-butanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-pro penyloxy)phenoxy)pentyl)oxime, nD24.5 1.5280
(583) 3-methyl-2-butanone O-(6-(2,6-dichloro-4-(3,3-dichloro-2-pro penyloxy)phenoxy)hexyl)oxime, nD24.5 1.5255
(584) 3-methyl-l-butanalO-(3-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime, nD24.5 1.5296
(585) trimethylacetaldehyde 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD23.0 1.5220
(586) 3,3-dimethyl-2-butanone O-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime, nD23.0 1.5281
(587) 3,3-dimethyl-2-butanoneO-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD23.0 1.5230
(588) 4-methyl-2-pentanone 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime, nD23.0 1.5295
(589) 4-methyl-2-pentanone 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD23.0 1.5203
(590) 4,4-dimethyl-2-pentanone 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime, nD23.0 1.5277
(591) 4,4-dimethyl-2-pentanone O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD23.0 1.5259
(592) 4,4-dimethyl-2-pentanone O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime, nD23.0 1.5205
(593) 4,4-dimethyl-2-pentanone O-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)oxime, nD23.0 1.5212
(594) 2-furaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl oxy)phenoxy)butyl)oxime, nD23.0 1.5690
(595) 2-thiophenecarbaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2 propenyloxy)phenoxy)butyl)oxime, nD23.0 1.5857

(596) 3-thiophenecarbaldehyde O-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD22.5. 1.5859
(597) l-methyl-2-pyrrolecarbaldehyde O-(4-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime, nD22.5 1.5802
(598) acetophenone 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyl)oxime
(599) acetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime
(600) acetophenone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime
(601) 4'-chloroacetophenone 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime
(602) 4'-chloroacetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(603) 4'-chloroacetophenone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(604) benzaldehyde O-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyl)oxime
(605) benzaldehyde 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyl oxy)phenoxy)butyl)oxime
(606) benzaldehyde 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime
(607) 4-chlorobenzaldehydeO-(3-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime
(608) 4-chlorobenzaldehydeO-(4-(2,6-diethyl-4-(3,3-dichloro-2-pro penyloxy)phenoxy)butyl)oxime
(609) 4-chlorobenzaldehyde O-(5-(2,6-diethyl-4-(3,3-dichloro-2-pro penyloxy)phenoxy)pentyl)oxime

(610) 4-(trifluoromethyl)benzaldehyde 0-(3-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)propyl)oxime
(611) 4-(trifluoromethyl)benzaldehyde 0-(4-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime
(612) 4-(trifluoromethyl)benzaldehydeO-(5-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime
(613) acetophenone 0-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyl)oxime
(614) acetophenone 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime
(615) acetophenone 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime
(616) 4'-chloroacetophenone O-(3-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime
(617) 4'-chloroacetophenoneO-(4-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime
(618) 4'-chloroacetophenone O-(5-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime
(619) 4'-(trifluoromethyl)acetophenone O-(3-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)propyl)oxime
(620) 4'-(trifluoromethyl)acetophenone 0-(4-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime
(621) 4'-(trifluoromethyl)acetophenoneO-(5-(2,6-diethyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime
(622) hexanalO-(4-(2,6-diethyl-4-(3,3-dichloro-2.propenyloxy)phe-noxy)butyl)oxime
(623) hexanal O-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)oxime

(624) trimethylacetaldehyde 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(625) trimethylacetaldehyde 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(626) 4-methyl-2-pentanone 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(627) 4-methyl-2-pentanone 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(628) 3,3-dimethyl-2-butanone O-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(629) 3,3-dimethyl-2-butanoneO-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(630) 3-methyl-2-butanone O-(4-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime
(631) 3-methyl-2-butanone O-(5-(2,6-diethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime
(632) benzaldehydeO-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime
(633) benzaldehyde 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime
(634) benzaldehyde 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime
(635) 4-chlorobenzaldehydeO-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime
(636) 4-chlorobenzaldehydeO-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(637) 4-chlorobenzaldehyde O-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime

(638) 4-(trifluoromethyl)benzaldehyde 0-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime
(639) 4-(trifluoromethyl)benzaldehyde 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(640) 4-(trifluoromethyl)benzaldehyde 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxiine
(641) acetophenone 0-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime
(642) acetophenone 0-(4-(2-ethyl-6-niethyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime
(643) acetophenone 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime
(644) 4'-chloroacetophenoneO-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime
(645) 4'-chloroacetophenone 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(646) 4'-chloroacetophenone 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(647) 4'-(trifluoromethyl)acetophenone 0-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime
(648) 4'-(trifluoromethyl)acetophenone 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(649) 4'-(trifluoromethyl)acetophenone 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(650) hexanal 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)butyl)oxime
(651) hexanal 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime

(652) trimethylacetaldehyde 0-(4-(2-ethyl-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxime
(653) trimethylacetaldehyde 0-(5-(2-ethyl-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime
(654) 4-methyl-2-pentanoneO-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(655) 4-methyl-2-pentanoneO-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(656) 3,3-dimethyl-2-butanone 0-(4-(2-ethyl-6-methyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime
(657) 3,3-dimethyl-2-butanone 0-(5-(2-ethyl-6-methyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime
(658) 3-methyl-2-butanone O-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(659) 3-methyl-2-butanone 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(660) benzaldehyde 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime
(661) benzaldehyde 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-
- penyloxy)phenoxy)butyl)oxime
(662) benzaldehyde 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime
(663) 4-chlorobenzaldehyde O-(3-(2-chloro-6-inethyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)propyl)oxime
(664) 4-chlorobenzaldehyde 0-(4-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxime
(665) 4-chlorobenzaldehyde 0-(5-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime

(666) 4-(trifluoromethyl)benzaldehyde 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime
(667) 4-(trifluoromethyl)benzaldehyde 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(668) 4-(trifluoromethyl)benzaldehyde 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(669) acetophenone 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)propyl)oxime
(670) acetophenone 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-
' penyloxy)phenoxy)butyl)oxime
(671) acetophenone 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)pentyl)oxime
(672) 4'-chloroacetophenone 0-(3-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)propyl)oxime
(673) 4'-chloroacetophenone O-(4-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxime
(674) 4'-chloroacetophenone 0-(5-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime
(675) 4'-(trifluoromethyl)acetophenone 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)oxime
(676) 4'-(trifluoromethyl)acetophenone 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(677) 4'-(trifluoromethyl)acetophenone 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(678) hexanal O-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyl oxy)phenoxy)butyl)oxime
(679) hexanal O-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)pentyl)oxime

(680) trimethylacetaldehydeO-(4-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxiine
(681) trimethylacetaldehyde O-(5-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime
(682) 4-methyl-2-pentanone 0-(4-(2-chloro-6-inethyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)butyl)oxime
(683) 4-methyl-2-pentanone O-(5-(2-chloro-6-methyl-4-(3,3-dichlo-ro-2-propenyloxy)phenoxy)pentyl)oxime
(684) 3,3-dimethyl-2-butanone 0-(4-(2-chloro-6-methyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)butyl)oxime
(685) 3,3-dimethyl-2-butanone 0-(5-(2-chloro-6-methyl-4-(3,3-di-chloro-2-propenyloxy)phenoxy)pentyl)oxime
(686) 3-methyl-2-butanone 0-(4-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime
(687) 3-inethyl-2-butanone O-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)oxime
(688) methyl 3-pyridyl ketone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD19.5 1.5715
(689) methyl 2-pyridyl ketone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD19.5 1.5717
(690) 4-(N,N-dimethylamino)benzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, IND19.5 1.5817
(691) 4-cyanobenzaldehyde 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime, m.p., 71.2°C
(692) 4'-nitroacetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime, nD19.0 1.5878
(693) 3'-nitroacetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxiine, nD19.0 1.5719

(694) 2'-nitroacetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-pro-penyloxy)phenoxy)butyl)oxime, nD20.5 1.5615
(695) methyl 4-pyridyl ketone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)oxime, nD20.5 1.5586
The following is a production example for the intermediate
compounds of formula (12).
Intermediate Production Example 1 Production of intermediate
compound 2)
First, 10.0 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 14,0 g of 1,3-dibromopropane, and 50 ml of N,N-dimethylformamide were placed in a reaction vessel, to which 5.3 g of potassium carbonate was added. After stirring at room temperature for 12 hours, the reaction mixture was filtered. The filtrate was poured into diluted hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate layer was washed twice with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 6.1 g (yield, 43%) of l-(3-bromopropyloxy)-2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)benzene.
Then, 10.0 g of l-(3-bromopropyloxy)-2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)benzene obtained in the same manner as described above, 4.0 g of N-hydrox5rphthalimide, and 100 ml of N,N-dimethylformamide were placed in a reaction vessel, to which 3.4 g of potassium carbonate was added. After stirring at room temperature for 12 hours, the reaction mixture was poured into ice water, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was washed with hexane, which afforded 9.4 g (yield, 78.3%) of N-(3-(2,6-dichloro-4-(3,3-di-

chloro-2-propenyloxy)phenoxy)propyloxy)phthalimide, m.p., 97.3°C.
Then, 9.1 g of N-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)-phenoxy)propyloxy)phthalimide was added to 150 ml of methanol, to which 1.9 g of hydrazine hydrate was added. The reaction mixture was stirred for 1 hour with heating under reflux, and returned to room temperature. To the reaction mixture was added 50 ml of water, from which the methanol was evaporated under reduced pressure. Further added were 15 ml of concentrated hydrochloric acid and 25 ml of water. The reaction mixture was stirred for 30 minutes with heating under reflux, returned to room temperature, and filtered. The crystals collected by filtration were added to 10% aqueous sodium hydrogencarbonate solution, and extracted with diethyl ether. The diethyl ether layer was washed with 10% aqueous sodium hydrogencarbonate solution and water. To this diethyl ether layer was added 3 ml of concentrated hydrochloric acid, and the mixture was concentrated and the dried, which afforded 6.8 g (yield, 92%) of 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)hydroxylamine hydrochloride, m.p., 171.8°C.
Some specific examples of the intermediate compounds of formula (12) are shown below with their compound numbers and physical properties, if any.
1) 0-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-
V
yl)hydroxylamine hydrochloride, m.p., 172.2°C
2) 0-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)hydroxylamine hydrochloride, m.p., 171.8°C
3) 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyl)hydroxylamine hydrochloride, m.p., 105,3°C
4) 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyl)hydroxylamine hydrochloride, m.p., 82.8°C

5) 0-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyl)hydroxylamine hydrochloride, m.p., 94.0°C
6) 0-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-
pyl)hydroxylamine hydrochloride
7) 0-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyl)hydroxylamine hydrochloride
8) 0-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyl)hydroxylamine hydrochloride
9) 0-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex-yl)hydroxylamine hydrochloride
10) 0-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyl)hydroxylamine hydrochloride
11) 0-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)butyl)hydroxylamine hydrochloride
12) 0-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)hydroxylamine hydrochloride
13) 0-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyl)hydroxylamine hydrochloride
14) 0-(3-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)propyl)hydroxylamine hydrochloride
15) 0-(4-(2-chloro-6-methyl-4-(3,3-dichlorO-2-propenyloxy)phe-noxy)butyl)hydroxylamine hydrochloride
16) 0-(5-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)pentyl)hydroxylamine hydrochloride
17) 0-(6-(2-chloro-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe-noxy)hexyl)hydroxylamine hydrochloride
The following are production examples for the carbonyl compounds of formula (22) including the intermediate compounds of formula (13) or (14) in

the present invention.
Intermediate Production Example 2 Production of intermediate
compound 18)
First, 2.06 g of terephthalaldehyde and 20 ml of ethanol were placed in a reaction vessel, to which 0.15 g of sodium borohydride was slowly added with stirring under ice cooling. After stirring at room temperature for 12 hours, the ethanol was evaporated. The residue was poured into diluted hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate layer was washed twice with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 1.06 g (yield, 51%) of p-(hydroxy-methyl)benzaldehyde.
To a mixture of 3.40 g of p-(hydroxymethyl)benzaldehyde obtained in the same manner as described above, 7,2 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 6.56 g of triphenylphosphine, and 50 ml of tetrahydro-furan was slowly added dropwise 5.05 g of diisopropyl azodicarboxylate with stirring under ice cooling. After stirring at room temperature for 12 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 4.75 g (yield, 46%) of 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyl)benzaldehyde, m.p., 93.9°C.
Intermediate Production Example 3 Production of intermediate compound 23)
First, 10.0 g of 2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenol, 14.0 g of 1,3-dibromopropane, and 50 ml of N,N-dimethylformamide were placed in a reaction vessel, to which 5.3 g of potassium carbonate was added. After stirring at room temperature for 12 hours, the reaction mixture was filtered. The filtrate was poured into diluted hydrochloric acid, and

extracted with ethyl acetate. The ethyl acetate layer was washed twice with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 6.1 g (yield, 43%) of l-(3-bromopropyloxy)-2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)benzene.
Then, 1.50 g of l-(3-bromopropyloxy)-2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)benzene obtained in the same manner as described above, 0.50 g of p-hydroxyacetophenone, and 30 ml of N,N-dimethylformamide were placed in a reaction vessel, to which 0.56 g of potassium carbonate was added. After stirring at room temperature for 24 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 1.51 g (yield, 89%) of 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)propyloxy)acetophenone, m.p., 73.6°C.
Intermediate Production Example 4 Production of intermediate compound 35)
A mixture of 15.67 g of 4-bromophenetyl alcohol, 6.88 g of 3,4-dihydro-2H-pyran, a catalytic amount of p-toluenesulfonic acid monohydrate, and 100 ml of tetrahydrofuran was stirred at room temperature for 24 hours. The reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure, which afforded 21.5 g (yield, 97%) of 4-(2-(2-tetrahydropyranyloxy)ethyl)-l-bromo-benzene, m.p., 93.9°C.

A mixture of 11,3 g of 4-(2-(2-tetrahydropyranyloxy)ethyl)-l-bromo-benzene and 100 ml of tetrahydrofuran was cooled to -78°C, to which 25.9 ml of 1.56 M solution of n-butyl lithium in n-hexane was added dropwise over 15 minutes. After stirring at -78°C for 1 hour, 4.2 ml of N,N-dimethyl-formamide was added dropwise at the same temperature over 15 minutes. After further stirring at -78°C for 1 hour, 100 ml of saturated aqueous ammonium chloride solution was added, and the stirring was further continued until the reaction mixture came to room temperature. The reaction mixture was extracted twice with 200 ml of ethyl acetate, and the ethyl acetate layers were combined, washed three times with saturated aqueous ammonium chloride solution, and washed with saturated aqueous sodium chloride solution. The combined ethyl acetate layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give a residue. This residue was subjected to silica gel chromatography, which afforded 7.20 g (yield, 78%) of 4-(2-(2-tetrahydropyranyloxy)ethyl)-benzaldehyde, nS24.5 1.5311.
A mixture of 6.50 g of 4-(2-(2-tetrahydropyranyloxy)ethyl)benzalde-hyde, 130 ml of acetone, and 110 ml of IM hydrochloric acid was stirred at room temperature for 24 hours. The reaction mixture was neutralized by the addition of saturated aqueous sodium hydrogencarbonate solution, and extracted twice with 200 ml of ethyl acetate. The ethyl acetate layers were combined, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give a residue. This residue was purified by silica gel chromatography, which 3.88 g (yield, 93%) of 4-(2-hydroxyethyl)benzaldehyde.
'H-NMR (CDCI3/TMS) 6 (ppm): 1.42-1.88 (6H, m), 2.99 (2H, t), 3.42-3.49 (1H, m), 3.60-3.74 (2H, m), 3.94-4.04 (1H, m), 4.58-4.60 (1H, m), 7.38-7.43 (2H, m), 7.79-7.84 (2H, m), 9.98 (1H, s)

To a mixture of 3.88 g of 4-(2-hydroxyethyl)benzaldehyde, 6,7 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 100 ml of tetrahydrofuran, and 6.0 g of triphenylphosphine was added dropwise a solution of 4.7 g of diisopropyl azodicarboxylate dissolved in 20 ml of tetrahydrofuran at the ice temperature over 1 hour. After completion of the addition, the reaction mixture was stirred at room temperature for 24 hours, and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, which afforded 6.63 g (yield, 69%) of 4-(2-(2,6-dichloro-4-(3,3-di-chloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde, m.p., 54.2°C.
Intermediate Production Example 5 Production of intermediate compound 37)
First, 11.1 g of l-(3-bromopropyloxy)-2,6-dichlorO-4-(3,3-dichloro-2-propenyloxy)benzene, 3.31 g of benzoic acid, and 50 ml of N,N-dimethyl-formamide were placed in a reaction vessel, to which 3.90 g of potassium carbonate was added. After stirring at room temperature for 24 hours, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. this crude product was subjected to silica gel chromatography, which afforded 11.6 g (yield, 95%) of 3,5-dichloro-4-(3-benzoyloxypropyloxy)-l-(3,3-dichloro-2-propenyloxy)benzene.
This 11.6 g of 3,5-dichlorO-4-(3-benzoyloxypropyloxy)-l-(3,3-dichloro-2-propenyloxy)benzene, 15.2 g of 10% aqueous potassium hydroxide solution, and 300 ml of methanol were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was concentrated. The concentrate was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product.

This crude product was subjected to silica gel chromatography, 7.41 g (yield, 83%) of 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-l-propyl alcohol.
Then, 2.00 g of 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-noxy)-l-propyl alcohol obtained in the same manner as described above and 20 ml of tert-butyl methyl ether were placed in a reaction vessel, to which 0.24 g of sodium hydride (60% in oil) was slowly added with stirring under ice cooling. After 10 minutes, 0.9 g of 5-acetyl-2-chloropyridine (which had been produced in Reference Production Example 1 as described below) was added, and the mixture was stirred at room temperature for 1 hour and further stirred in an oil bath at 80°C (internal temperature). After 5 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which 0.62 g (yield, 23%) of 5-acetyl-2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)pyridine, m.p., 90.5°C.
Intermediate Production Example 6 Production of intermediate compound 52)
To a mixture of 56.3 g of 1,4-butanediol and 400 ml of N,N-dimeth-ylformamide was slowly added 11.0 g of 60% sodium hydride (in oil) with stirring under ice cooling. After stirring at room temperature for 12 hours, 49.3 g of bromoacetaldehyde diethylacetal was added dropwise, and the stirring was further continued at 60°C for 8 hours. The reaction mixture was poured into ice water, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 21.6 g

(yield, 41%) of 4-(2,2-diethoxyethoxy)butanol.
To a mixture of 2.30 g of 4-(2,2-diethoxyethoxy)butanol, 2.94 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 2.94 g of triphenylphosphine, and 30 ml of tetrahydrofuran was slowly added dropwise 2.48 g of diisopro-pylazodicarboxylate with stirring in a stream of nitrogen gas under ice cooling. After stirring at room temperature for 24 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 4.48 g (yield, 73%) of 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene.
Then, 1.81 g of 3,5-dichloro-l-(3,3-dichlorO-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene was added to a mixture of 10 ml of acetic acid and 1 ml of concentrated hydrochloric acid with stirring under ice cooling, and the stirring was further continued for 15 minutes. The reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, saturated aqueous sodium hydrogencarbonate solution, and saturated aqueous sodium chloride solution in this order, dried over anhydrous magnesium sulfate, and concentrated, which afforded 1.51 g (yield, 94%) of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde.
'H-NMR (CDCI3/TMS) 6 (ppm): 1.92 (4H, m), 3.65 (2H, t), 3,99 (2H, t), 4.09 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.84 (2H, s), 9.75 (1H, s)
Intermediate Production Example 7 Production of intermediate compound 57)
To a mixture of 16,0 g of 4-(2,2-diethoxyethoxy)butanol, 18.9 g of 2,6-diehtyl-4-benzoylox5T)henol (which had been produced according to the method as described in JP-A 8-337549/1996), 20.2 g of triphenylphosphine, and 200 ml of tetrahydrofuran was slowly added dropwise 17.0 g of diisopro-pyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen

gas. After stirring at room temperature for 6 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 31.4 g (yield, 88%) of 3,5-diethyM-benzoyl-oxy-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene, nD24.8 1.5129.
To a solution of 31.0 g of 3,5-diethyl-l-benzoyloxy-4-(4-(2,2-diethoxy-ethoxy)butyloxy)benzene dissolved in 100 ml of methanol was added a solution of 5,1 g of potassium hydroxide dissolved in 25 g of water. After stirring at room temperature for 1 hour, the reaction mixture was acidified by the addition of diluted hydrochloric acid, and concentrated. The residue was poured into water, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 0.60 g (yield, 94%) of 3,5-diethyl-4-(4-(2,2-diethoxyethoxy)butyloxy)phenol, nD25.0 1.4890.
Then, 19.9 g of 3,5-diethyl-4-(4-(2,2-diethoxyethoxy)butyloxy)phenol, 9.20 g of 1,1,3-trichloro-l-propene, 9.15 g of potassium carbonate, and 200 ml of N,N-dimethylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium, and concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 25.4 g (yield, 91%) of 3,5-diethyl-l-(3,3-di-chloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene, nD26.0 1.4991.
To a mixture of 9.27 g of 3,5-diethyl-l-(3,3-dichloro-2-propenyloxy)-4-(4-(2,2-diethoxyethoxy)butyloxy)benzene, 25 ml of acetic acid, and 5 ml of water was added 1 ml of concentrated hydrochloric acid at room temperature.

After stirring at room temperature for 30 minutes, the reaction mixture was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, aqueous sodium hydrogen-carbonate solution, and aqueous sodium chloride solution in this order, dried over anhydrous magnesium sulfate, and concentrated, which afforded 7.62 g (yield, 98%) of 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-oxyacetaldehyde.
'H-NMR (CDCI3/TMS) 6 (ppm): 1.22 (6H, t), 1.88 (4H, m), 2.63 (4H, q), 3.63 (2H, t), 3.74 (2H, t), 4.09 (2H, s), 4.61 (2H, d), 6.14 (1H, t), 6.57 (2H, s), 9.75 (1H, s)
Intermediate Production Example 8 Production of intermediate compound 68)
First, 65.1 g of 1,5-pentanediol, 18.6 g of proparygyl chloride, 12.0 g of sodium hydroxide (powdery), 5.69 g of benzyltriethylammonium chloride, and 200 ml of tetrahydrofuran were placed in a reaction vessel, and reaction mixture was stirred for 4 hours with heating under reflux. The reaction mixture was filtered through Celite, and the filtrate was poured into water, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 12.4 g (yield, 35%) of 5-(2-pro-pynyloxy)pentanol, nD26.3 1.4533.
To a mixture of 2.35 g of 5-(2-propynyloxy)pentanol, 4.32 g of 2,6-di-chloro-4-(3,3-dichloro-2-propenyloxy)phenol, 4.33 g of triphenylphosphine, and 30 ml of tetrahydrofuran was slowly added dropwise 3.64 g of diisopro-pyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen gas. After stirring at room temperature for 24 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel

chromatography which afforded 5.17 g (yield, 84%) of 3,5-dichloro-l-(3,3-di-chloro-2-propynyloxy)-4-(5-(2-propynyloxy)pentyloxy)benzene, nD25.5 1.5400.
A mixture of 4.12 g of 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(2-propenyloxy)pentyloxy)benzene, 0.36 g of mercury (II) sulfate, 5 ml of 1% aqueous sulfuric acid solution, and 50 ml of tetrahydrofuran was stirred at 60°C for 1 hour. The reaction mixture was filtered through Celite, and the filtrate was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with diluted hydrochloric acid and water in this order, dried over magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 4.05 g (yield, 94%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone,
ND25.5' 1.5350.
Intermediate Production Example 9 Production of intermediate compound 99)
First, 16.3 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 20,7 g of potassium carbonate, 11.8 g of ethyl 5-bromovalerate, and 200 ml of N,N-dimethylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was filtered. The filtrate was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which 18.9 g (yield, 80%) of ethyl 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyl-oxy)phenoxy)valerate, nD24.0 1.5331.
To a mixture of 4.06 g of ethyl 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)valerate and 50 ml of toluene was added dropwise 10.27 ml of 0.95 mol/liter diisobutyl aluminum hydride (hexane solution)

over 30 minutes with stirring at -70°C in a stream of nitrogen gas. After further stirring at -70°C for 1 hour, 50 ml of saturated aqueous ammonium chloride solution was added. The reaction mixture was returned to room temperature, and poured into50 ml of diluted hydrochloric acid, and extracted twice with toluene. The toluene layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 3.52 g (yield, 96%) of 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal.
'H-NMR (CDCI3/TMS) 6 (ppm): 1.80-2.11 (4H, brs), 2.58 (2H, t), 3.99 (2H, t), 4.62 (2H, d), 6.13 (1H, t), 6.85 (2H, d), 9.81 (1H, s)
Intermediate Production Example 10 Production of intermediate compound 96)
First, 8.64 g of 2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenol, 4.98 g of potassium carbonate, 3.36 g of chloroacetone, and 50 ml of N,N-di-methylformamide were placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture was filtered. The filtrate was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 10.12 g (yield, 98%) of (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy-acetone, m.p., 83.8**C.
Some specific examples of the carbonyl compounds of formula (22) including the intermediate compounds of formula (13) or (14) of the present invention are shown below with their compound numbers and their physical
properties, if any.
18) 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-
yl)benzaldehyde, m.p., 93.9°C
19) 4-((2,6-dichloro-4-(3,3-dibromo-2-propenyloxy)phenoxy)meth-

yl)benzaldehyde
20) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
ethoxy)benzaldehyde, m.p., 81.3°C
21) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)benzaldehyde, m.p., 76.5°C
22) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-tyloxy)benzaldehyde, m.p., 54.9°C
23) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)acetophenone, m.p., 73.6°'C
24) 4'-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyloxy)acetophenone, glassy
25) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-
pyloxy)benzaldehyde, Nd24.5 1.5809
26) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyloxy)benzaldehyde, nD24.5 1.5770
27) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-
pyloxy)benzophenone nD24.5 1.5928
28) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)propiophenone, m.p., 39.8°C
29) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)valerophenone, nD24.5 1.5703
V
30) 4-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen-tyloxy)benzaldehyde, m.p., 41.4°C
31) 4'-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
pentyloxy)acetophenone, m.p., 101.0°C
32) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-
yloxy)acetophenone, m.p., 100.1°C
33) 3-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-

yl)benzaldehyde
1H-NMR (CDCI3/TMS) 6 (ppm): 4.61 (2H, d), 5.06 (2H, s), 6.13 (1H, t), 6.89 (2H, s), 7.58 (1H, t), 7.86 (1H, dt), 7.87 (1H, dt), 8.05 (1H, t), 10.06 (1H,
s)
34) 4'-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxymeth-
yl)acetophenone, m.p., 88.6°C
35) 4-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-
yl)benzaldehyde, m.p., 54.2°C
36) 4-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-
yl)phenoxyacetaldehyde
37) 5-acetyl-2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-
noxy)propyloxy)pyridine, m.p., 90.5°C
38) 4-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)benzaldehyde, m.p., 61.0°C
39) 4-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)but-yl)benzaldehyde
40) 4'-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-yl)-2,2,2-trifluoroacetophenone
41) 4'-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)eth-yl)-2,2,2-trifluoroacetophenone
42) 4'-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyl)-2,2,2-trifluoroacetophenone
43) (2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxy)-5-pyridyl)acetaldehyde
44) (2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxy)-5-pyridyl)acetaldehyde
45) 2-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pyloxy)-5-pyridyl phenyl ketone

46) 2-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyloxy)-5-pyridyl phenyl ketone
47) 5-((2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)meth-
yl)-2-furfural
48) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-
yl)-2-thiophenecarboxaldehyde
49) 5-((2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)meth-
yl)-2-pyrrolcarboxaldehyde
50) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
ethoxyacetaldehyde
51) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-
oxyacetaldehyde
^H-NMR (CDCI3/TMS) 6 (ppm): 2.15 (2H, t), 3,83 (2H, t), 4.08 (2H, t), 4.12 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.84 (2H, s), 9.74 (1H, s)
52) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl
oxyacetaldehyde
'H-NMR (CDCI3/TMS) 5 (ppm): 1.92 (4H, m), 3.65 (2H, t), 3.99 (2H, t), 4.09 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.84 (2H, s), 9.75 (1H, s)
53) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-
oxyacetaldehyde
'H-NMR (CDCI3/TMS) 6 (ppm): 1.59-1.77 (4H, brs), 1.86 (2H, brs), 3.58 (2H, t), 3.96 (2H, t), 4.07 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.83 (2H, s), 9.74 (1H, s)
54) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-
oxyacetaldehyde
'H-NMR (CDCI3/TMS) δ(ppm): 1.4-1.9 (8H, m), 3.55 (2H, t), 3.95 (2H, t), 4.06 (2H, s), 4.58 (2H, d), 6.11 (1H, t), 6.83 (2H, s), 9.74 (1H, s)
55) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-

acetaldehyde
56) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-
oxyacetaldehyde
57) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-
oxyacetaldehyde
^H-NMR (CDCI3/TMS) 6 (ppm): 1.22 (6H, t), 1.88 (4H, m), 2.63 (4H, q), 3.63 (2H, t), 3.74 (2H, t), 4.09 (2H, s), 4.61 (2H, d), 6.14 (1H, t), 6.57 (2H, s),
9.75 (1H, s)
58) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-
oxyacetaldehyde
1H-NMR (CDCI3/TMS) 6 (ppm): 1.22 (6H, t), 1.60-1.82 (6H, brs), 2.63 (2H, q), 3.58 (2H, t), 3.71 (2H, t), 4.07 (2H, s), 4.61 (2H, d), 6.14 (1H, t), 6.57 (2H, s), 9.74 (1H, s)
59) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxyphenoxy)hexyl-
oxyacetaldehyde
60) 2-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetaldehyde
61) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-propyloxyacetaldehyde
62) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-butyloxyacetaldehyde
63) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-pentyloxyacetaldehyde
64) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-hexyloxyacetaldehyde
65) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxyacetone
66) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-

oxyacetone
67) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-
oxyacetone
68) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-
oxyacetone, nD25.5 1.5350
69) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-
oxyacetone
70) 2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethoxy-
acetone
71) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl-
oxyacetone
72) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl-
oxyacetone
73) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl-
oxyacetone
74) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl-
oxyacetone
75) 2-(2-ethyl-6-inethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
ethoxyacetone
76) 3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
propyloxyacetone
77) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
butyloxyacetone
78) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
pentyloxyacetone
79) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
hexyloxyacetone
80) 3-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-

ethoxy)propionaldehyde
81) 3-(3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-
pyloxy)propionaldehyde
82) 3-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu-
tyloxy)propionaldehyde
83) 3-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen tyloxy)propionaldehyde
84) 3-(6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex yloxy)propionaldehyde
85) 3-(2-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy) ethoxy)propionaldehyde
86) 3-(3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro
pyloxy)propionaldehyde
87) 3-(4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)bu
tyloxy)propionaldehyde
88) 3-(5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pen
tyloxy)propionaldehyde
89) 3-(6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hex
yloxy)propionaldehyde
90) 3-(2-(2-ethyl-6-inethyl-4-(3,3-dichloro-2-propenyloxy)phe
noxy)ethoxy)propionaldehyde
91) 3-(3-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe noxy)propyloxy)propionaldehyde
92) 3-(4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe noxy)butyloxy)propionaldehyde
93) 3-(5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe noxy)pentyloxy)propionaldehyde
94) 3-(6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phe

noxy)hexyloxy)propionaldehyde
95) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-
hyde
96) (2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone,
m.p., 83.8°C
97) 3-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-
pionaldehyde
1H-NMR (CDCI3/TMS) δ (ppm): 2.91 (2H, dt), 4.33 (2H, t), 4.59 (2H,
d), 6.11 (1H, t), 6.85 (2H, s), 9.97 (1H, d)
98) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)buta-
nal
1H-NMR (CDCI3/TMS) 6 (ppm): 2.14 (2H, tt), 2.80 (2H, t), 3.99 (2H, t), 4.58 (2H, d), 6.11 (1H, t), 6.83 (2H, s), 9.88 (1H, s)
99) 5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-
nal
'H-NMR (CDCI3/TMS) δ (ppm): 1.80-2.11 (4H, brs), 2.58 (2H, t), 3.99 (2H, t), 4.62 (2H, d), 6.13 (1H, t), 6.85 (2H, d), 9.81 (1H, s)
100) 6-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexa-
nal
1H-NMR (CDCI3/TMS) 6 (ppm): 1.50-1.95 (6H, brs), 2.48 (2H, t), 3.95 (2H, t), 4.58 (2H, d), 6.11 (1H, t), 6.83 (2H, s), 9.79 (1H, s)
101) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetalde-
hyde
102) (2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)acetone
103) 3-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)pro-pionaldehyde
104) 4-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal
105) 5-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)penta-

nal
106) 6-(2,6-diethyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal
107) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
acetaldehyde
108) (2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
acetone
109) 3-(2-ethyl-6-methyl-4-(3,3-dichlorO-2-propenyloxy)phenoxy)-
propionaldehyde
110) 4-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
butanal
111) 5-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
pentanal
112) 6-(2-ethyl-6-methyl-4-(3,3-dichloro-2-propenyloxy)phenoxy)-
hexanal
113) 2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)aceto-
phenone, m.p., 112.5°C
114) 7-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)heptyl-oxyacetone
115) 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-2-bu-tenyloxyacetone
116) 2-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethoxy)ethoxyacetone
117) 2-(N-(2-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)-ethyl)-N-methylamino)ethoxyacetone
118) 4-(2,6-dichloro-4-(3,3-dichlorO-2-propenyloxy)phenoxy)cyclo-hexyloxyacetone
The following are production examples for the intermediate compounds of formula (15).

Intermediate Production Example 11 Production of intermediate compound 138)
First, 0.56 g of 2,6-dichlorO-4-benzoyloxyphenol (which can be produced according to the method as described in JP-A 8-337549/1996), 0.30 g of potassium carbonate, 0.74 g of 5-(methanesulfonyloxy)pentyloxy-acetone 0-tert-butyloxime, and 10 ml of N,N-dimethylformamide are placed in a reaction vessel. After stirring at room temperature for 24 hours, the reaction mixture is poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-dichloro-4-(benzoyloxy)phenoxy)pentyloxyacetone 0-tert-butyloxime.
To a solution of 0.99 g of 5-(2,6-dichloro-4-(benzoyloxy)phenoxy)-pentyloxyacetone 0-tert-butyloxime dissolved in 7.5 ml of methanol is added a solution of 0.15 g of potassium hydroxide dissolved in 1.5 ml of water. After stirring at room temperature for 1 hour, the reaction mixture is acidified by the addition of diluted hydrochloric acid, and concentrated. Water is added to the residue, and the mixture is extracted twice with ethyl acetate. The ethyl acetate layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-(2,6-di-chloro-4-hydroxyphenoxy)pentyloxyacetone 0-tert-butyloxime.
Some specific examples of the intermediate compounds of formula (15) are shown below with their compound numbers and their physical properties, if any.
119) 4-(2,6-dichloro-4-hydroxyphenoxy)butanal 0-isopropyloxime
120) 5-(2,6-dichloro-4-hydroxyphenoxy)pentanal 0-isopropyloxime

121) 6-(2,6-dichloro-4-hydroxyphenoxy)hexanal 0-isopropyloxime
122) 4-(2,6-dichloro-4-hydroxyphenoxy)butanal O-tert-butyloxime
123) 5-(2,6-dichloro-4-hydroxyphenoxy)pentanal 0-tert-butyl-oxime
124) 6-(2,6-dichloro-4-hydroxyphenoxy)hexanal 0-tert-butyloxime
125) 4-(2,6-dichloro-4-hydroxyphenoxy)butanal 0-(2,2,2-trichloro-ethyl)oxime
126) 5-(2,6-dichloro-4-hydroxyphenoxy)pentanal 0-(2,2,2-trichlo-roethyl)oxime
127) 6-(2,6-dichloro-4-hydroxyphenoxy)hexanal 0-(2,2,2-trichloro-ethyl)oxime
128) 4-(2,6-dichloro-4-hydroxyphenoxy)butanalO-(3,3-dichloro-2-propenyl)oxime
129) 5-(2,6-dichloro-4-hydroxyphenoxy)pentanal O-(3,3-dichloro-2-propenyl)oxiine
130) 6-(2,6-dichloro-4-hydroxyphenoxy)hexanal 0-(3,3-dichloro-2-propenyl)oxime
131) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetaldehyde O-isopropyloxime
132) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetaldehyde O-isopropyloxime
133) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetone O-isopropyloxime
134) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetone O-isopropyloxime
135) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-tert-butyloxime
136) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetaldehyde

0-tert-butyloxime
137) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetone 0-tert-butyloxime
138) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetone 0-tert-butyloxime
139) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetaldehyde O- (2,2,2-trichloroethyl)oxime
140) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime
141) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetone 0-(2,2,2-trichloroethyl)oxime
142) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetone 0-(2,2,2-trichloroethyl)oxime
143) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
144) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime
145) 4-(2,6-dichloro-4-hydroxyphenoxy)butyloxyacetone 0-(3,3-di-chloro-2-propenyl)oxime
146) 5-(2,6-dichloro-4-hydroxyphenoxy)pentyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime
147) 4-(2,6-dichloro-4-hydroxyphenoxymethyl)benzaldehyde 0-sec-butyloxime
148) 4-(2,6-dichloro-4-hydroxyphenoxymethyl)benzaldehyde
0-t-butyloxime
149) 4-(2-(2,6-dichloro-4-hydroxyphenoxy)ethyl)benzaldehyde
0-sec-butyloxime
150) 4-(2-(2,6-dichloro-4-hydroxyphenoxy)ethyl)benzaldehyde

0-allyloxime
151) 4-(2-(2,6-dichloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)oxime
152) 4-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-n-propyloxime
153) 4-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-isopropyloxime
154) 4-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)benzaldehyde O-sec-butyloxime
155) 4-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-t-butyloxime
156) 4'-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)acetophe-none 0-ethyloxime
157) 4'-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)propiophe-none O-ethyloxime
158) 4'-(4-(2,6-dichloro-4-hydroxyphenoxy)butyloxy)acetophenone O-ethyloxime
159) 4'-(4-(2,6-dichloro-4-hydroxyphenoxy)butyloxy)acetophenone 0-n-propyloxime
160) 4-(4-(2,6-dichloro-4-hydroxyphenoxy)butyloxy)benzaldehyde 0-isopropyloxime
161) 4'-(3-(2,6-dichloro-4-hydroxyphenoxy)propyloxy)-2,2,2-trifluo-roacetophenone O-ethyloxime
162) 4-(trifluoromethyl)benzaldehyde 0-(4-(2,6-dichloro-4-hy-droxyphenoxy)butyl)oxime
163) 4'-(trifluoromethyl)acetophenone 0-(4-(2,6-dichloro-4-hy-droxyphenoxy)butyl)oxime
164) trimethylacetaldehyde 0-(5-(2,6-dichloro-4-hydroxyphe-

noxy)pentyl)oxime
165) 3,3-dimethyl-2-butanone 0-(5-(2,6-dichloro-4-hydroxyphe-noxy)pentyl)oxime
166) 3,3-dimethyl-2-butanone 0-(4-(2,6-dichloro-4-hydroxyphe-noxy)butyl)oxime
167) 4-methyl-2-pentanone 0-(4-(2,6-dichloro-4-hydroxyphenoxy)-butyl)oxime
168) 4-methyl-2-pentanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)-pentyl)oxime
169) 3-methyl-2-butanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)-pentyl)oxime
Reference Production Example 1 Production example for 5-acetyl-2-chloropyridine used in Intermediate Production Example 5
First, 15.45 g of 6-chloronicotinic acid and 100 ml of diethyl ether were placed in a reaction vessel, to which 131 ml of methyl lithium (1.5 M ether solution) was slowly added dropwise with stirring under ice cooling (internal temperature, O°C to -5°C). After completion of the addition, the reaction mixture was further stirred at room temperature for 24 hours, and concentrated. The residue was poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concen-trated. This crude product was subjected to silica gel chromatography, which 13.11 g (yield, 86%) of 5-acetyl-2-chloropyridine.
The following are production examples for the intermediate r compounds of formula (21)
Reference Production Example 2 Production of 0-(3,3-dichloro-2-propenyl)hydroxylamine hydrochloride
To a mixture of 44 g of N-hydroxyphthalimide, 39 g of potassium

carbonate, and 400 ml of N,N-dimethylformamide was added 41 g of 1,1,3-trichloro-1-propene at room temperature. After stirring at room temperature for 12 hours, the reaction mixture was poured into diluted hydrochloric acid to cause the deposition of crystals. These crystals were collected by filtration, washed with water and hexane in this order, and dried under reduced pressure, which afforded 66 g (yield, 90%) of N-(3,3-dichloro-2-propenyloxy)phthalimide.
To a mixture of 66 g of N-(3,3-dichloro-2-propenyloxy)phthalimide and 300 ml of chloroform was slowly added dropwise a mixture of 13 g of hydrazine hydrate and 17 ml of isopropyl alcohol at room temperature. After stirring 3 hours with heating under reflux, the reaction mixture was returned to room temperature, in which 100 ml of hexane was poured. The reaction mixture was filtered, and the filtrate was concentrated to give a residue, in which 100 ml of hexane was again poured. This hexane solution was again filtered, and hydrogen chloride gas was blown in the filtrate to cause the deposition of crystals. These crystals were collected by filtration, and dried under reduced pressure, which afforded 26 g (yield, 60%) of 0-(3,3-dichloro-2-propenyl)hydroxylamine hydrochloride.
'H-NMR (CDCl3-CD30D/TMS)(5(ppm): 4.76 (2H, s), 6.17 (1H, t)
Reference Production Example 3 Production of 0-(3-(5-trifluoro-methyl-2-pyridyloxy)propyl)hydroxylamine
To a mixture of 12.6 g of 1,3-propanediol and 100 ml of N,N-dimethyl-formamide was added in portions 3.30 g of 60% sodium hydride (in oil) at room temperature over 30 minutes with stirring in a stream of nitrogen gas. After further stirring at room temperature for 1 hour, a solution of 10.0 g of 2-chloro-5-trifluoromethylpyridine in 20 ml of N,N-dimethylformamide was added dropwise over 40 minutes. After further stirring at room temperature overnight, 100 ml of about 2 N diluted hydrochloric acid was added over

15 minutes to complete the reaction. The reaction mixture was extracted twice with 500 ml of toluene in total. The toluene layers were combined, washed with diluted hydrochloric acid and saturated aqueous sodium hydrogencarbonate solution in this order, dried over anhydrous magnesium sulfate, and concentrated to give 9.70 g of oil. This oil was dissolved with heating in 300 ml of hexane, followed by recrystallization, which afforded 5.3 g (yield, 44%) of 2-(3-hydroxypropyloxy)-5-trifluoromethylpyridine, m.p., 46.6°C.
To a mixture of 20.0 g of 2-(3-hydroxypropyloxy)-5-trifluoromethyl-pyridine, 14.7 g of N-hydroxyphthalimide, 23.6 g of triphenylphosphine, and 200 ml of tetrahydrofuran was slowly added dropwise 20.0 g of diisopropyl azodicarboxylate with stirring under ice cooling in a stream of nitrogen gas. After stirring at room temperature for 24 hours, the reaction mixture was concentrated to give a residue. This residue was subjected to silica gel chromatography, which afforded 27.8 g (yield, 84%) of N-(3-(5-trifluoro-methyl-2-pyridyloxy)propyloxy)phthalimide, m.p., 97.6°C.
To a mixture of 12,8 g of N-(3-(5-trifluoromethyl-2-pyridyloxy)propyl-oxy)phthalimide and 150 ml of chloroform was slowly added dropwise a mixture of 1.74 g of hydrazine hydrate and 1.5 ml of isopropyl alcohol at room temperature. After stirring for 3 hours with heating under reflux, the reaction mixture was returned to room temperature, in which 150 ml of hexane was poured. The reaction mixture was filtered through Celite, and the filtrate was concentrated to give a residue, in which 100 ml of hexane was again poured. This hexane solution was left stand in a refrigerator in 3 days. The deposited crystals were collected by filtration, and dried under reduced pressure, which afforded 7.0 g (yield, 85%) of 0-(3-(5-trifIuoro-methyl-2-pyridyloxy)propyl)hydroxylamine, nD24.0 1,4652.
Reference Production Example 4 0-(2,2,2-trichloroethyl)hydroxyl-

amine hydrochloride
To a mixture of 2.99 g of 2,2,2-trichloroethanol, 2.15 g of 0-(2,4,6-tri-methylbenzenesulfonyl)hydroxylamine (which had been produced according to the method as described in Synthesis, 1-17 (1977)), and 20 ml of diethyl ether was slowly added 0.68 g of sodium ethoxide with stirring under ice cooling. After stirring at room temperature for 5 hours, the deposited precipitate was removed by Celite filtration, and hexane was added to the filtrate. This hexane solution was bubbled with a blow of hydrogen chloride gas at room temperature to case the deposition of crystals. These crystals were collected by filtration, and dried under reduced pressure, which afforded 1.18 g (yield, 59%) of 0-(2,2,2-trichloroethyl)hydroxylamine hydrochloride.
^H-NMR (CDCI3-CD3OD/TMS) 6 (ppm): 4.84 (2H, s) The following are production examples for the intermediate compounds of formula (20).
Reference Production Example 7 Production of compound 170) First, 5.21 g of 1,5-pentanediol is placed in a reaction vessel, to which 0.22 g of 60% sodium hydride (in oil) is slowly added at room temperature with stirring in a stream of nitrogen gas. After stirring at room temperature until the evolution of hydrogen gas ceases, 0.75 g of chloroacetaldehyde 0-tert-butyloxime is added at room temperature, and the reaction mixture is slowly warmed to 50°C. After further stirring at 50°C for 3 hours, the reaction mixture is poured into water, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, diluted hydrochloric acid, and water in this order, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product is subjected to silica gel chromatography, which affords 5-hydroxypentyloxy-aldehyde 0-tert-butyloxime.

Reference Production Example 8 Production of intermediate compound 171
First, 13.02 g of 1,5-pentanediol, 2.40 g of sodium hydroxide (powdery), 1.14 g of benzyltriethylammonium chloride, and 100 ml of tetra-hydrofuran were placed in a reaction vessel, to which 8.18 g of chloroacetone 0-tert-butyloxime was slowly added dropwise with stirring under heating under reflux. After further stirring for 8 hours, the reaction mixture was poured into diluted hydrochloric acid, and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with diluted hydrochloric acid and water in this order, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 6.79 g (yield, 59%) of 5-hydroxy-pentyloxyacetone 0-tert-butyloxime, nD23.2 1.4493.
Some specific examples of the intermediate compounds of formula (20) are shown below with their compound numbers and their physical properties, if any.
170) 5-hydroxypentyloxyacetaldehyde 0-tert-butyloxime
171) 5-hydroxypentyloxyacetone 0-tert-butyloxime
172) 4-hydroxybutyloxyacetone 0-tert-butyloxime
173) 4-hydroxy-2-butenyloxyacetone 0-tert-butyloxime
174) 4-hydroxy-2-butynyloxyacetone 0-tert-butyloxime
175) 2-(2-hydroxyethoxy)ethoxyacetone 0-tert-butyloxime, nD24.7 1.4451
176) 2-(N-2-hydroxyethyl-N-methylamino)ethoxyacetone 0-tert-butyloxime
177) 4-hydroxycyclohexyloxyacetone 0-tert-butyloxime
178) l-(5-hydroxypentyloxy)-2-butanone 0-tert-butyloxime, nD23.4 1.4479

179) l-(5-hydroxypentyloxy)pinacolone 0-tert-butyloxime, UD^^^ 1.4451
180) 2-(5-hydroxypentyloxy)acetophenone 0-tert-butyloxime, nD23.2 1.5090
181) 2-(5-hydroxypentyloxy)cyclohexanone 0-tert-butyloxime
The following are production examples for the intermediate
compounds of formula (19). The intermediate compounds produced in Reference Production Example 10 or 12 can also be used as the starting material in Reference Production Example 7, and the intermediate compounds produced in Reference Production Example 11 or 13 can also be used as the starting material in Reference Production Example 8.
Reference Production Example 9 Production of intermediate compound 182)
To 2.94 g of 40% aqueous chloroacetaldehyde solution was added 2.94 g of 0-(3,3-dichloro-2-propenyl)hydroxylamine hydrochloride with stirring at room temperature. After stirring at room temperature for 2 hours, the reaction mixture was extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 1.94 g (yield, 96%) of chloroacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD23.2 1.5038.
Reference Example 10 Production of intermediate compound 183)
To 9.81 g of 40% aqueous chloroacetaldehyde solution was added 3.77 g of 0-tert-butylhydroxylamine hydrochloride with stirring at room temperature. After stirring at room temperature for 2 hours, the reaction mixture was extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which afforded 4.21 g (yield, 94%) of chloroacetaldehyde 0-tert-butyloxime, UD23.2 1.4418.

Reference Production Example 11 Production of intermediate compound 184)
A mixture of 1.51 g of 0-tert-butylhydroxylamine hydrochloride, 0.93 g of chloroacetone, and 10 ml of diethyl ether is stirred at room temperature for 3 hours, poured into water, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords chloroacetone 0-tert-butyloxime,
Reference Production Example 12 Production of intermediate compound 183)
To 3.92 g of 40% aqueous chloroacetoaldehyde solution is 2.08 g of hydroxylamine hydrochloride with stirring at room temperature. After stirring at room temperature for 24 hours, the reaction mixture is extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords 1.32 g (yield, 71%) of chloroacetoaldehyde oxime.
Then, 0.47 g of chloroacetoaldehyde oxime, 0.1 ml of concentrated sulfuric acid, and 10 ml of diethyl ether are placed in a reaction vessel, into which isobutene gas is blown with stirring under ice cooling, and the stirring is further continued at room temperature. After completion of the reaction, the reaction mixture is slowly poured into saturated aqueous sodium hydro-gencarbonate solution, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with 10% aqueous sodium hydroxide solution and water in this order, dried over anhydrous magnesium sulfate, and concentrated, which affords chloroacetoaldehyde 0-tert-butyloxime.
Reference Production Example 13 Production of intermediate compound 184)
A mixture of 0.83 g of hydroxylamine hydrochloride, 0.93 g of chloro-

acetone, and 10 ml of diethyl ether is stirred at room temperature for 3 hours, poured into water, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords chloroacetone oxime.
Then, 0.54 g of chloroacetone oxime, 0.1 ml of concentrated sulfuric acid, and 10 ml of diethyl ether are placed in a reaction vessel, into which isobutene gas is blown with stirring under ice cooling, and the reaction mixture is further stirred at room temperature. After completion of the reaction, the reaction mixture is slowly poured into saturated aqueous sodium hydrogencarbonate solution, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with 10% aqueous sodium hydroxide solution and water in this order, dried over anhydrous magnesium hydroxide, and concentrated, which affords chloroacetone 0-tert-butyloxy-oxime.
Reference Production Example 14 Production of intermediate compound 189)
First, 0.22 g of 5-hydroxypentyloxyaldehyde 0-tert-butyloxime, 0.12 g of triethylamine, and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which 0.14 g of methanesulfonyl chloride is slowly added dropwise with stirring under ice cooling. After completion of the addition, the reaction mixture is further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords 5-(methane-sulfonyloxy)pentyloxyaldehyde 0-tert-butyloxime.
Reference Production Example 15 Production of intermediate compound 190)
First, 0.23 g of 5-hydroxypentyloxyacetone 0-tert-butyloxime, 0.12 g

of triethylamine, and 10 ml of tetrahydrofuran are placed in a reaction vessel, to which 0.14 g of methanesulfonyl chloride is slowly added with stirring under ice cooling. After completion of the addition, the reaction mixture is further stirred at room temperature for 30 minutes, poured into diluted hydrochloric acid, and extracted twice with diethyl ether. The diethyl ether layers are combined, washed with water, dried over anhydrous magnesium sulfate, and concentrated, which affords 5-(methanesulfonyloxy)pentyloxy-acetone 0-tert-butyloxime.
Some specific examples of the intermediate compounds of formula (19) are shown below with their compound numbers and their physical properties, if any. Intermediate compounds 182) to 188) can also be sued as the starting materials for the production of intermediate compounds 170) to 181) of formula (19).
183) 184) 185) 186) 187) 188) 189)
182) chloroacetaldehyde 0-(3,3-dichloro-2-propenyl)oxime, nD 23.2 1.5038
chloroacetaldehyde 0-tert-butyloxime, nD23.2 1.4418 chloroacetone 0-tert-butyloxime l-bromo-2-butanone 0-tert-butyloxime 1-bromopinacolone 0-tert-butyloxime 2-chloroacetophenone 0-tert-butyloxime 2-chlorocyclohexanone 0-tert-butyloxime 5-(methanesulfonyloxy)pentyloxyacetaldehyde 0-tert-butyl

oxime
oxime

190) 5-(methanesulfonyloxy)pentyloxyacetone 0-tert-butyloxime
191) 4-(methanesulfonyloxy)butyloxyacetone 0-tert-butyloxime
192) 4-(methanesulfonyloxy)-2-butenyloxyacetone 0-tert-butyl
193) 4-(methanesulfonyloxy)-2-butynyloxyacetone 0-tert-butyl-

oxime
194) 2-(2-(methanesulfonyloxy)ethoxy)ethoxyacetone 0-tert-butyl-oxime
195) 2-(N-2-(methanesulfonyloxy)ethyl-N-methylamino)ethoxy-acetone 0-tert-butyloxime
196) 4-(methanesulfonyloxy)cyclohexyloxyacetone 0-tert-butyloxime
197) l-(5-(methanesulfonyloxy)pentyloxy)-2-butanone 0-tert-butyloxime
198) l-(5-(methanesulfonyloxy)pentyloxy)pinacolone 0-tert-butyloxime
199) 2-(5-(methanesulfonyloxy)pentyloxy)acetophenone 0-tert-butyloxime
200) 2-(5-(methanesulfonyloxy)pentyloxy)cyclohexanone 0-tert-butyloxime
The following are formulation examples in which -parts- are by weight and the present compounds are designated by their compound numbers as described above.
Formulation Example 1 Emulsifiable concentrates
First, 10 parts of each of the present compounds (1) to (687) is dissolved in 35 parts of xylene and 35 parts of N,N-dimethylformamide, to which 14 parts of polyoxyethylene styrylphenyl ether and 6 parts of calcium dodecylbenzenesulfonate are added. The mixture is well stirred to give a 10% emulsifiable concentrate of each compound.
Formulation Example 2 Wettable powders
First, 20 parts of each of the present compounds (1) to (687) is added to a mixture of 4 parts of sodium lauryl sulfate, 2 parts of calcium lignin sulfonate, 20 parts of synthetic hydrated silicon oxide fine powder, and

54 parts of diatomaceous earth. The mixture is stirred with a mixer to give a 20% wettable powder of each compound.
Formulation Example 3 Granules
To five parts of each of the present compounds (1) to (687) are added 5 parts of synthetic hydrated silicon oxide fine powder, 5 parts of sodium dodecylbenzenesulfonate, 30 parts of bentonite, and 55 parts of clay, and the mixture is well stirred. A suitable amount of water is added to the mixture, which is further stirred, granulated with a granulator, and air-dried to give a 5% granule of each compound.
Formulation Example 4 Dusts
First, 1 part of each of the present compounds (1) to (687) is dissolved in a suitable amount of acetone, to which 5 parts of synthetic hydrated silicon oxide fine powder, 0.3 part of PAP, and 93.7 parts of clay are added, and the mixture is stirred with a mixer. The removal of acetone by evaporation gives a 1% dust of each compound.
Formulation Example 5 Flowables
First, 20 parts of each of the present compounds (1) to (687) is mixed with 1.5 parts of sorbitan trioleate and 28.5 parts of an aqueous solution containing 2 parts of polyvinyl alcohol. The mixture is pulverized into fine particles having a particle size of not more than 3 µm with a sand grinder, to which 40 parts of an aqueous solution containing 0.05 part of xanthan gum and 0.1 part of aluminum magnesium silicate is added and then 10 parts of propylene glycol is added. The mixture is stirred to give a 20% flowable of each compound.
Formulation Example 6 Oil sprays
First, 0.1 part of each of the present compounds (1) to (687) is dissolved in 5 parts of xylene and 5 parts of trichloroethane. The solution is mixed with 89.9 parts nf deodorized kerosine to give a 0.1% oil spray of each

compound.
Formulation Example 7 Oil-based aerosols
First, 0.1 part of each of the present compounds (1) to (687), 0.2 part of tetramethrin, 0.1 part of d-phenothrin, and 10 parts of trichloroethane are dissolved in 59.6 parts of deodorized kerosine, and the solution is put in an aerosol vessel. The vessel is equipped with a valve, through which 30 parts of a propellant (liquefied petroleum gas) is charged under increased pressure to give an oil-based aerosol of each compound.
Formulation Example 8 Water-based aerosols
An aerosol vessel is filled with a mixture of 0.2 part of each of the present compounds (1) to (687), 0.2 part of d-allethrin, 0.2 part of d-phenothrin, 5 parts of xylene, 3,4 parts of deodorized kerosine, and 1 part of an emulsifier (ATMOS 300 available from Atlas Chemical Co.); and 50 parts of pure water. The vessel is equipped with a valve, through which 40 parts of a propellant (liquefied petroleum gas) are charged under increased pressure to give a water-based aerosol of each compound.
Formulation Example 9 Mosquito-coils
First, 0.3 g of each of the present compounds (1) to (687) is mixed with 0.3 g of d-allethrin, and the mixture is dissolved in 20 ml of acetone. The solution is uniformly mixed with 99.4 g of a carrier for mosquito-coils (prepared by mixing Tabu powder, pyrethrum marc powder and wood flour in the ratio of 4 : 3 : 3) under stirring. The mixture is well kneaded with 120 ml of water, molded, and dried to give a mosquito-coil of each compound.
Formulation Example 10 Electric mosquito-mats
First, 0.4 g of each of the present compounds (1) to (687), 0.3 parts of d-allethrin, and 0.4 g of pipenyl butoxide are dissolved in acetone to have a total volume of 10 ml. Then, 0.5 ml of the solution is uniformly absorbed in a substrate for electric mosquito-mats having a size of 2.5 cm x 1.5 cm and a

thickness of 0.3 cm (prepared by forming a fibrillated mixture of cotton linter and pulp into a sheet) to give an electric mosquito-mat of each compound.
Formulation Example 11 Heating smoke formulations
First, 100 mg of each of the present compounds (1) to (687) is dissolved in a suitable amount of acetone. The solution is absorbed in a porous ceramic plate having a size of 4.0 cm x 4.0 cm and a thickness of 1.2 cm to give a heating smoke formulation of each compound.
Formulation Example 12: Poison baits
First, 10 mg of each of the present compounds (1) to (687) is dissolved in 0.5 ml of acetone, and the solution is uniformly mixed with 5 g of solid bait powder for animals (Breeding Solid Feed Powder CE-2 available from Japan Clea Co., Ltd.). The removal of acetone by air drying gives a 0.5% poison bait of each compound.
The following test examples are provided for demonstrating that the present compounds are useful as active ingredients of insecticidal/acaricidal agents. In these test examples, the present compounds are designated by their compound numbers as describe above and the compounds used for comparison are designated by their compound symbols as described below.
Compound (A): 4-(3-chloro-2-propenyloxy)phenoxyacetone 0-ethyl-oxime (i.e., compound 9 as described in JP-A 61-72733, page 7)
Compound (B): 4-phenoxy-benzaldehyde 0-(3-methylbutyl)oxime (i.e., compound 41 as described in JP-A 61-260054, page 4)
Test Example 1 Insecticidal test against Spodoptera litura
A 200-fold water dilution (500 ppm) of a test compound formulation obtained according to Formulation Example 1 or 2 was absorbed at a volume of 2 ml in an artificial diet (Insecta LF available from Nihon Nosan K.K.) having a weight of 13 g, which had been prepared in a polyethylene cup having a diameter of 11 cm. Five fourth-instar larvae of Spodoptera litura

were set free in the cup. After 6 days, the survival of the larvae was examined to determine the mortality.
As a result, it was found that the present compounds (1)-(31), (33), (34), (47), (74).(76), (90), (91), (103), (104), (131), (133), (134), (147)-(150), (152)-(186), (203), (279)-(393), (481), (523)-(556), (558)-(572), (574)-(597), and (688)-(695) exhibited a mortality of 80% or higher. In contrast, compounds (A) and (B) exhibited the mortality of 0%.
Test Example 2 Insecticidal test against Plutella xylostella To a water dilution (50 ppm) of a test compound formulation obtained according to Formulation Example 1 was added a spreading agent (New RINOU available from Nihon Noyaku K.K,) at a dilution ratio of 3000-fold. The dilution was sprayed over potted cabbages at the four to five leaf stage at a volume of 25 ml per pot. After the treated plants were air dried, ten third-instar larvae of Plutella xylostella were set free on each pot. After 4 days, the mortality was determined.
As a result, it was found that the present compounds (l)-(22), (24)-(29), (33), (34), (47), (75), (76), (90), (91), (103), (104), (134), (153)-(161), (163)-(176), (180), (182)-(185), (279), (281), (283), (285), (287)-(299), (301)-(313), (315)-(321), (327), (332), (334), (336), (338)-(342), (351)-(360), (362)-(368), (370), (372)-(374), (376)-(382), (384)-(389), (391)-(393), (523), (524), (528)-(550), (558)-(566), (568)-(570), (573), (574), (576)-(579), (581)-(584), (589), (591)-(597), and (689)-(693) exhibited a mortality of 80% or higher. In contrast, compound (A) exhibited the mortality of 0%,
Test Example 3 Insecticidal test against Heliothis virescens
A water dilution (100 ppm) of a test compound formulation obtained
according to Formulation Example 1 was added dropwise at a volume of
0.2 ml and uniformly spread over the surface of an artificial diet having a
weight of 3 g, which had been prepared in a 30 ml plastic cup. After air

drying, one second-instar larva of Heliothis virescens was set free in each cup. Ten larvae were used for each treatment. After 7 days, the mortality of the larvae was determined.
As a result, it was found that the present compounds (3), (5), (11), (14)-(17), (25)-(27), (33), (34), (47), (76), (90), (91), (104), (134), (153)-(156), (160), (161), (163)-(169), (171)-(175), (281)-(300), (305)-(310), (312)-(331), (338)-(343), (346), (347), (350)-(359), (523), (528)-(531), (533)-(540), (542)-(551), (559), and (561)-(564) exhibited a mortality of 80% or higher.
Test Example 4 Insecticidal test against Helicoverpa armigera A cotton leaf fragment (diameter, 5 cm) was immersed for 10 seconds in a water dilution (100 ppm) of a test compound formulation obtained according to Formulation Example 1. This fragment was taken out from the dilution, air dried, and placed in a polyethylene cup having a diameter of 5.5 cm. One third-instar larva of Helicoverpa armigera was set free in each cup. Ten larvae were used for each treatment. After 5 days, the mortality of the larvae was determined.
As a result, it was found that the present compounds (2)-(6), (11), (14), (17), (24)-(26), (91), (104), (279), (283), (288), (291), (293), (303), (312), (318), (327), (329), (342), (355), (357), (358), (529), (531), (545), (562), (564), and (582) exhibited a mortality of 80% or more. In contrast, compound (A) exhibited the mortality of 0%.
Test Example 5 Insecticidal test against Cydia pomonella A water dilution (100 ppm) of a test compound formulation obtained according to Formulation Example 1 was added dropwise at a volume of 0.2 ml and spread over the surface of an artificial diet having a weight of 3 g, which had been prepared in a 30 ml polyethylene cup. After air drying, placed in the cup was a piece of wax paper (about 2.5 cm square) having about 20 eggs which had been laid by Cydia pomonella and were just before

hatching. Four pieces of such wax paper were used for each treatment. After 7 days, the mortality of the larvae was determined.
As a result, it was found that the present compounds (l)-(3), (6), (10), (11), (14)-(16), (25), (27), (33), (34), (47), (76), (90), (91), (153)-(156), (158)-(176), (279), (289)-(291), (293), (294), (297), (300), (306), (307), (309)-(315), (317)-(319), (323), (324), (326)-(331), (338)-(340), (352)-(359), (365), (378), (379), (381), (382), (481), (528)-(531), (533)-(540), (542)-(546), (549), (550), (558)-(566), (568)-(570), (572), (574), (575), (578), and (579) exhibited a mortality of 80% or higher.
Test Example 6 Acaricidal test against Tetranychus urticae
About twenty female adults of Tetranychus urticae were set free on brush bean {Phaseolus vulgaris) in the primary leaf stage, which had been potted in a plastic cup for 7 days after the seeding. After 6 days, a 200-fold water dilution (500 ppm) of a test compound formulation obtained according to Formulation Example 1 or 2 was sprayed at a volume of 15 ml over the plant. After 8 days, each compound was evaluated for acaricidal activity on the following criteria.
almost no damage and completely no surviving mites slight damage and some few surviving mites
+: rather smaller damage and a rather fewer surviving mites than non-treatment case
++: same as non-treatment case
As a result, it was found that the present compounds (6), (104), (173), (178), (306), (318), (327), (542), (582), (583), (589), (592), and (593) were evaluated at --- or -±-. In contrast, compounds (A) and (B) were evaluated at-+-.
Test Example 7 Insecticidal test against Musca domestica
In the bottom of a polyethylene cup having a diameter of 5.5 cm was

placed a piece of filter paper having the same size. A 200-fold water dilution (500 ppm) of a test compound formulation obtained according to Formulation Example 1 was added dropwise at a volume of 0.7 ml on the filter paper, and about 30 mg of sucrose as a diet was uniformly placed thereon. Ten female adults of houseflies {Musca domestica) were set free in the cup, and the cup was kept covered. After 1 day, the survival of the adults was determined to determine the mortality.
As a result, it was found that the present compounds (1), (4), (6), (7), (11)-(16), (18), (19), (22), (28), (29), (153), (155), (158), (159), (165)-(167), (170), (173), (175), (176), (180), (203), (287), (305), (307), (309), (318), (330), (332), (372)-(374), (376), (378), (481), (541), (542), (545), (551), (560), (565), (566), and (689) exhibited a mortality of 80% or higher. In contrast, compounds (A) and (B) used for comparison exhibited the mortality of 0%.
Industrial Applicability The present compounds have excellent insecticidal/acaricidal activity, so that they are satisfactorily effective for the control of noxious insects, mites and ticks.

44. The oxime compound according to claim 5, 29, 30, 31, 32, 33,
34, 35, 36, 37, or 38, wherein A1 is A1-12.
45. The oxime compound according to claim 40, wherein G2 is
oxygen.
46. The oxime compound according to claim 41, wherein Q1 is
oxygen.
47. The oxime compound
oxygen.
48. The oxime compound according to claim 5, 29, 30, 31, 32, 33,
I 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, or 47, wherein G1 is G1-1.
49. The oxime compound according to claim 5, 29, 30, 31, 32, 33,
34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, or 47, wherein G1 is G1-2.
50. The oxime compound according to claim 49, wherein Q2 is
oxygen.
) 51. The oxime compound according to claim 5, 29, 30, 31, 32, 33,
35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50, wherein R^ is
hydrogen, Ci-Cg alkyl, Cg-Cg haloalkyl, C-y^i al'co* ;], C^-CG haloiillienyl.
C3-C6 alkynyl, or C3-C6 haloalkynyl,
or C3-C7 cycloalkyl optionally
or C4-C10 cycloalkylalkyl optionally substituted the ring thereof,
or C6-C6 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C6-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on the ring thereof
52. The oxime compound according to claim 5, 29, 30, 31, 32, 33,
35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50, wherein R6 is
T1-l or T1-2.
53. The oxime compound according to claim 5, 29, 30, 31, 32, 33,

35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49. or 50, wherein R^ is hydrogen.
54. The oxime compound according to claim 5, 29, 30, 31, 32, 33.
35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46,
C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, or
55. The oxime compound according to
are independently halogen or C1-C3 alkyl;
R4 is 3,3-dichloro-2-propenyl; a is 0;
Y and Z are both oxygen;
R6 is C1-C5 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl or C3-C6 haloalkenyl; AMsA'-7;
G1 is G1-.l;
al is 0;
W is 1,3-phenylene or 1,4-phenylene,
h and p are both 0; and
R19, R20, R25, R26, R29, abd R30 ARE ALL hydrogen.
56. The oxime compound according to claim 5, wherein R2 and R3
are independently halogen or C1-C3 alkyl;
R4 is 3,3-dichloro-2-propenyl; a is 0;
Y and Z are both oxygen;
R6 is C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl or C3-C6 haloalkenyl;
A1 is A1-8
G1 is G1-1;
al is 0;
G2 is oxygen;

or a heterocyclic 6-membered ring, exclusive of pyridine ring, containing at least one oxygen, sulfur, or nitrogen atom, which heterocyclic 6-membered ring may be optionally substituted with one to three identical or different (R16)g's wherein R18 and g are as defined in claim 1,
or a heterocyclic 5-membered ring containing at least one oxygen, sulfur, or nitrogen atom, which heterocyclic 5-membered ring may be optionally substituted with one to three identical or different (R18)g'8 wherein R18

of which heterocyclic rings may be optionally substituted with one to three identical or different (R18)g s wherein R18 and g are as defined in claim 1,
or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring.
59. The oxime compound according to claim 3, wherein R8 and R9 are independently hydrogen, C1-C11 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C5 haloalkynyl, C2-C6 alkoxyalkyl, or C2-C10 alkylthioalkyl,

67. The oxime compound according to claim 3, 67, 58, 59, 61, 62,
or 63, wherein A1 is A1--4.
68. The oxime compound according to claim 3, 67, 58, 69, 61, 62,

or 63, wherein A2 is A2-5.
69. The oxime compound 59, 61, 62,
or 63, wherein A2 is A2-6.
70. The oxime compound according to claim 3, 57, 58, 59, 61, 62,
or 63, wherein A2 is A2-7 or A2-9.
71. The oxime compound according to claim 3, 57, 58, 59, 61, 62,

are both 0; and R19, R20 R25 R26 R27, R25 R31, and R32 are all hydrogen.
83. The oxime compound wherein h and p
are both 0; and R19 R20, R25 R26, R29, R30, R36
84. The oxime compound according to
are both 0; and R19 R20, R25, R26 R29 R30, R35 and R36 are all hydrogen.
85. The oxime compound according to claim 79, wherein h and p
are both 0; and R19 R20, R25, R26, R27, R28, R31, R32 R35, and R6 me all

95. The compound according to claim 1, which is 5-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal O-tert-butyloxime.
96. The compound according to claim 1, which is 6-(2,6-dichloro-
4-(3.3-dichloro-2-propenyloxy)phenoxy)hexanal 0-tert-butyloxime.
97. The compound according to claim 1, which is 4-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal 0-(2,2,2'-trichlovoethyl)-
oxime.
98. The compound according to claim 1, which is 5-(2,6-dichloro-

4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal 0-(2,2,2-trichloroethyl)-oxime,
99. The compound according to claim 1, which is 6-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal 0-(2,2,2-trichloroethyl)
oxime.
100. The compound according to claim 1, which is 4-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal 0 (3, 7 dichloro-2-propenyl)-
oxime.
101. The compound according to claim 1, which is 5-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanal 0-(3,3-dichloro-2-propenyl)-
oxime.
102. The compound according to claim 1, which is 6-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal 0-(3,3-dichloro-2-propenyl)-
oxime.
103. The compound according to claim 1, which is 1-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-isopropyl-
oxime.
104. The compound according to claim 1, which is 5-(2,6-dichlo
4-(3,3-dichloro-2-propenyloxy)phenoxy)
oxime.
i
105. The compound according to claim 1, which is 4-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetone 0-isopropyloxime.
106. The compound according to claim 1, which is 5-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-isopropyloxime.
107. The compound according to claim 1, which is 4-(2,6-dichloro-
4-(3.3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-tert-butyl-
oxime.
108. The compound according to claim 1, which is 5-(2,6-dichloro-

4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde 0-tert-butyl-oxime.
109. The compound according to claim 1, which is 4-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetone 0-tert-butyloxime.
110. The compound according to
4-(3,3-dichloro-2-propenyloxy)phenoxy)
111. The compound according to claim 1, which is 4-(2,6-dichloro-
4-(3.3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-(2,2,2-tri-
chloroethyl)oxime.
112. The compound according to claim 1, which is 5-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde 0-(2,2,2-tri-
chloroethyl)oxime.
113. The compound according to claim 1, which is 4-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetone 0-(2,2,2-trichloro-
ethyl)oxime.
114. The compound according to claim 1, which is 5-(2.6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)
ethyl)oxime.
115. The compound according to claim 1, which is 4-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde 0-(3,3-dichlo-
ro-2-propenyl)oxime,
116. The compound according to claim 1, which is 5-(2,6-dichlon)
4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde 0-(3,3-dichlo'
ro-2-propenyl)oxime.
117. The compound according to claim 1, which is '4-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetone 0-(3,3-dichloro-2-
propenyl)oxime.
118. The compound according to claim 1, which is 5-(2,6-dichloro-

4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime.
119. The compound according to claim 1, which is 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyib3nzaldehyde 0-sec-butyl-oxime.
120. The compound according to claim 1, which is 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methylbenzaldehyde 0-t-butyl-oxime.
121. The compound according to claim 1, which is 4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde 0-sec-butyl-oxime.
122. The compound according to claim 1, which is 4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde 0-alIyloxime.
123. The compound according to claim 1, which is 4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde 0-(3,3-dichIo-ro-2-propenyl)oxime,
124. The compound according to claim 1, which is 4-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzaldehyde 0-n-pro-pyloxime.
125. The compound according to claim 1, which is 4-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzaldehyde 0-isopro-pyloxime.
126. The compound according to claim 1, which is 4-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzdldehyde 0-sec-
butyloxime.
127. The compound according to claim1, which is 4-(3-(2,β-clichlo
ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)prbonzaldehyde 0-t-buty)
oxime.

130. The compound according to claim 1, which is 4'-(4-(2,6-dichlo-
ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)acetophenone 0-ethyl-
oxime,
131. The compound according to claim 1, which is 4'-(4-(2,fl (lichlo
ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)acetophenone O-n-plo
pyloxime.
132. The compound according to claim 1, which is 4-(4-(2,6-dichulo-
ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)benzaldehyde 0-isopro-
pyloxime.
133. The compound according to claim 1, which is 4--(3-(2,6-di-
chloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)-2,2,2-trifluoro-
acetophenone 0-ethyloxime.
134. The compound according to claim 1, which is 4-(trifluoro-
methyl)benzaldehyde 0-(4-(2,6-dichlcro-4-(3,3-dichloro-2-propenyloxy)phe-
noxy)butyl)oxime.
135. The compound according to claim 1, which is 4'-(trifluoro-
methyl)acetophenone 0-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phe-
noxy)butyl)oxime,
136. The compound according to claim 1, which is trimethyl-
acetaldehyde 0-(5-(2,6-dichloro-4-(3,3-dichIoro-2-propenyloxy)phenoxy)pen-
tyl)oxime.

137. The compound according to claim 1 which is 3,3-dimethyl-2-
butanone O-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)ph8noxy)pentyl)-oxime.
138. The compound according to claim 1, which is 3,3-dimethyl-2-
butanoneO-(4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)-
oxime.
139. The compound according to claim 1, which is 4-methyl-2-
pentanone O-(4-(2,6-dichloro-4-(3.3-dichloro-2-propenyloxy)phenoxy)butyl)-
oxime.
140. The compound according to claim 1, which is 4-methyl-2-
pentanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)-
oxime.
141 The compound according to claim 1, which is 3'methyl-2-butanone 0-(5-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)-oxime.
142. An insecticidal/acaricidal agent comprising as an active
ingredient, an oxime compound according to any one of claims 1 to 141.
143. A method for the extermination of insects, ticks or mitrw,
comprising applying to the insects, ticks or mites, or to their habitats, an
effective amount of an oxime compound according to any one of claims 1 to
141.

R2 and R3 are both chlorine; R4 is 3,3-dichloro-2-propenyl; and R7 is hydrogen or methyl.
152. The compound according to claim 1, which is 4-(2,6-dlrhloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butanal oxime.
153. The compound according to claim 1, which is 5-(2,6-dichloro
4-(3,3-dichloro-2-propenyloxy)phenoxy)pentanai oxime.
154. The compound according to claim 1, which is 6-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)hexanal oxime.
155. The compound according to claim 1, which is 4-(2,6-dichloro-
4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde oxime.
156. The compound according to claim 1, which is 5-(2,6-dichloro-

4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxyacetaldehyde oxime.
157. The compound according to claim 1, which is 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy ace tone oxime.
158. A hydroxylamine compound of formula (12)

independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
h is an integer of 0 or 1;
j is an integer of 1 to 3;
m is an integer of 1 to 3;
n is an integer of 1 to 3;
p is an integer of 0 or 1;
t is an integer of 0 to 3;
u is an integer of 0 to 3;
fl is an integer of 1 to 3;
Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2;
E is C5-C6 cycloalkylene;
U3 is U3-1, U3-2, or U3-3 of formula (10)

wherein:
R35 and R36 are independently hydrogen, C1-C3 aikyi, or trifluoromethyl;
(R40)g1's are zero to four identical or different substi-tuents selected from halogen, G1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy;
R and V are independently -CH= or nitrogen;
gl is an integer of 0 to 4;
h1 is an integer of 1 to 3;
i is an integer of 2 or 3;

A2-8 or A2-10; or a salt thereof.
169. The hydroxylamine compound according to 161, wherein h and p are both 0; and R19 R20 R25 R26. R29 and R30 are all hydrogern or a salt thereof.

177. The amine compound according to claim 158, which is 0-(3-
(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyl)hydroxylamine
hydrochloride.
178. The amine compound according to claim 158, which is 0-(4-
(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyl)hydroxylamine
hydrochloride.
179. The amine compound according to claim 158, which is 0-(5-

(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyl)hydroxyJamin«i hydrochloride.
180. The amine compound according to claim 158, which is 0-(β-
(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)hexyl)hydroxylamine hydrochloride.
181. A compound of formula (13)

I /
haloalkyl, C1-C3 alkoxy, or C1-C8 haloalkoxy; and R19 and R20 are both hydrogen.
183. The compound according to claim 187, which is3,5-ditihloro-
l-(3,3-dichloro-2-propenyloxy)-4-(4-formylbenzyloxy)benzenoi
184. The compound according to claim 181, which is 3,5-dichlom-
l-(3,3-dichloro-2-propenyloxy)-4-(4-acetylbenzyloxy)benzene. :
185. The compound according to claim 185, which is 3,5-dichloro-
l-(3,3-dichloro-2-propenyloxy)-4-(4-formylphenethyloxy)benzene.
186. The compound according to claim 185, which is 3,5-dichloro-
l-(3,3-dichloro-2-propenyloxy)-4-(4-acetylphenethyloxy)benzene.
187. The compound according to claim 185, which is 3,5-dichloro-
l-(3,3-dichloro-2-propenyloxy)-4-(5-formyl-2-furylmethoxy)benzene.
188. A compound of formula (14)

R19 R20, R29 and R30 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
j is an integer of 1 to 3; and V is an integer of 1 to 4.
189. The compound according to claim 188, wherein R2 and R3 are
independently halogen or C1-C3 alkyl;
R7 is hydrogen, C1-C8 alkyl, or C1-C3 haloalkyl, or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy; and R19 R2o R29 and R30 are all hydrogen.
190. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(3-(4-formylphenoxy)propoxy)benzene.
191. The compound according to claim 188, which is 3,5-dichloro-1.-(3,3-dichloro-2-propenyloxy)-4-(4-(4-formylphenoxy)butoxy)benzene.
192. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-formylphenoxy)pentyloxy)benzene.
193. The compound according to claim 188, which is 3,5-dichloro-l'(3,3-dichloro-2-propenyloxy)-4-(3-(4-acetylphenoxy)propoxy)benzene.
194. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(4-(4-acetylphenoxy)batoxy)benzene.
195. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-acetylphenoxy)pentyioxy)bonzene.
196. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(3-(4-(trifluoroacetyl)phenoxy)propoxy)-benzene.
197. The compound according to claim 188, which is 3,5-dichloro-
■J ■ l-(3,3-dichloro-2-propenyloxy)-4-(4-(4-(trifluoroacetyl)phenoxy)butoxy)-
benzene.

198. The compound according to claim 188, which is 3.5-dichloro-
l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-(trifluoroacetyl)phenoxy)pentyloxy)-
benzene.
199. The compound according to claim IBS. whhichis 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(3-(4-propionylphenoxy)propoxy)benzene.
200. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(4-(4-propionylphenoxy)butoxy)benzene,
201. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-propionylphenoxy)pentyloxy)benzene.
202. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(3-(4-benzoylphenoxy)propoxy)benzene.
203. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(4-(4-benzoylphenoxy)butoxy)benzene.
204. The compound according to claim 188, which is 3,5-dichloro-l-(3,3-dichloro-2-propenyloxy)-4-(5-(4-benzoylphenoxy)petyloxy)benzene.
205. The compound according to claim i, winch is 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methylbenzaldehyde oxime.
206. The compound according to claim 1, which is 4'-((2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)methyl)acetophenone oxime.
207. The compound according to claim 1, which is 4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)benzaldehyde oxime.
208. The compound according to claim 1, which is .4-(2-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)ethyl)acetophenone oxime,
209. The compound according to claim 1, which is 4-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)benzaldehyde oxime.

210. The compound according to claim 1, which is 4-(4-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)bexbleyde oxime.
211. The compound according to claim 1, which is 4-(5-(2,6-dichlo-

ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)bonzaldehyde oxime.
212. The compound according to claina, (3-(2,6-dichlo-ro- 4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)acelophenone oxime.
213. The compound according to claim 1, which is 4'-(4-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)acetophenone oxime.
214. The compound according to claim 1, which is 4'-(5-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)acetophenone oxime.
215. The compound according to claim 1. which is 4'-(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)-2,2,24rifluoroacetophe-none oxime.
216. The compound according to claim 1, which is 4'-(4-(2,β illchlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)-2,2,2-trifluoroacetophe none oxime.
217. The compound according to claim 1, which is 4-(5-(2,6-diehlo-
ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)-2,2,2-trifluoroacetophe-none oxime.
218. The compound according to claim 1, which is 4'"(3-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyloxy)propiophenone oxime.
219. The compound according to claim 1, which is 4'-(4-(2,6-dichlo-
ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)propiophenone oxime.
220. The compound according to claim 1, which is 4'-(5-(2,6-dichlo-
ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)propiophenone oxime.
221. The compound according to claim 1, which is 4'-(3-(2,6-dichlo-
ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)propyioxy)ben2ophenone oxime.
222. The compound according to claim 1, which 4-(4-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxy)ben2ophenone oxime.
223. The compound according to claim 1, which is 4-(5-(2,6-dichlo-ro-4-(3,3-dichloro-2-propenyloxy)phenoxy)pentyloxy)benzophenone oxime.

224. A phenol compound of formula (50) wherein:
R1 R2, and R3 are independently halogen, C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1-C3 haloalkoxy, nitro, or cyano;
a is an integer of 0 to 2;
Z is oxygen, sulfur, or NR5 wherein R5 is hydrogen, acetyl, or C1-C3

D is -CH= or nitrogen; J is oxygen or sulfur; b is an integer of 0 to 5; d is an integer of 1 to 3; e is an integer of 0 to 3; f is an integer of 2 to 4;

alkyl, C1-C3 haloalkyl, C1-C4 alkoxy, or C1-C3 haloalkoxy; and R'16 and R42 are independently C1-C6 alkyl, C2-C6

wherein:
(R17)b's are zero to five identical or different substi-tuents selected from halogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C1-C6 alkoxy, C1-C3 haloalkoxy, C2-C6 alkenyloxy, C2-C6 haloalkenyloxy, C2-C6 alkynyloxy, C3-C6 haloalkynyloxy, C1-C3 alkylthio, C1-C3 haloalkylthio, C1-C2 alkylsulfinyl, C1-C2 alkylsulfonyl, C1-C2 haloalkylsulfinyl, CpCa haloalkylsulfonyl,

together at their ends to form trimethylene or tetramethyl-ene,
or when b is 2 to 5, two adjacent R17's are combined together at their ends to form methylenedioxy optionally substituted with halogen or C1-C3 alkyl,

or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring;

methyl;
R22 is hydrogen, C1-C3 alkyl, or trifluoromethyl,
or when h is 0 and i is 1 in A1-l, R22 and R7 may be combined together at their ends to form trimethylene, tetra-methylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl,
or when h is 0 and j is 1, in A1-2, A1-3, A1-4, A1-5, or A1-6, R22 and R2 may be combined together at their ends to form trimethylene, tetramethylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl;
h is an integer of 0 or 1;
i is an integer of 1 to 6;
j is an integer of 1 to 3;
k is an integer of 2 to 8;
m is an integer of 1 to 3;
n is an integer of 1 to 3;
p is an integer of 0 or 1;
q is an integer of 0 or 1;
r is an integer of 2 to 4;
s is an integer of 2 to 4;
t is an integer of 0 to 3;
u is an integer of 0 to 3;
V is an integer of 1 to 4;
w is an integer of 1 to 4;
X is an integer of 1 to 4;
Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2;
Q2 is oxygen, S(0)z, or NR34 wherein R34 is hydrogen

or C1-C3 alkyl, and z is an integer of 0 to 2; E is C5-C6 cycloalkylene; U1 is U1 of formula (6)
wherein:
W is an optionally substituted benzene ring or an optionally substituted heterocyclic ring;
G1 is G1-l or G1-2 of formula (7)

Q2 is oxygen, S(0)z,, or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2;
R35 R36 R37 and R38 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
al is an integer of 0 to 4;
bl is an integer of 1 to 3; and
dl is an integer of 0 to 2; and

are independently hydrogen, C1-C8 alkyl, or trifluoromethyl;
h is an integer of 0 or 1;
j is an integer of 1 to 3;
m is an integer of 1 to 3;
n is an integer of 1 to 3;
p is an integer of 0 or 1;
t is an integer of 0 to 3;
u is an integer of 0 to 3;
f1 is an integer of 1 to 3;
Q1 is oxygen, S(0)y, or NR33 wherein R33 is hydrogen or C1-C3 alkyl, and y is an integer of 0 to 2;
E is C6-C6 cycloalkylene;
U1 is U3.l, U3-2, or U3-3 of formula (10)

h1 is an integer of 1 to 3;
i1 is an integer of 2 or 3; and
Q2 is oxygen, S(0)„ or NR34 wherein R34 is
hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2;
U4 is U4-l, U4-2, or U'-3 of formula (11)

wherein:
R35 and R36 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
(R40)g1's are zero to four identical or different substituents selected from halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy;
R and V are independently -CH= or nitrogen;
gl is an integer of 0 to 4;
hi is an integer of 1 to 3;
il is an integer of 2 or 3;
Q2 is oxygen, S(0),, or NR34 wherein R34 is hydrogen or C1-C3 alkyl, and z is an integer of 0 to 2; and
Q3 is oxygen, S(0)e,i, or NR39 wherein R39 is
hydrogen or C1-C3 alkyl, and el is an integer of 0 to 2.
225. The phenol compound according to claim 224, wherein Z is

a is 0.
227. The phenol compound according to claim 224, 225, or 226,
wherein R1 R2 and R3 are independently halogen or C1-C3 alkyl.
228. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1
229. The phenol compound according to claim 224, 225, 226, or
227, wherein X is X2
230. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-l,
231. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-2.
232. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-3.
233. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-4.
234. The phenol compound according to claim 224, 225, 226, or
227, wherein X is X1 and A1 is A1-5.
1.
235: The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 arid A1 is A1-6.
236. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-7.
237. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-8.
238. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-9.
239. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X1 and A1 is A1-1O.
240. The phenol compound according to claim 224, 225, 226, or

227, wherein X is X^ and A' is A'-ll.
241. The phenol compound according to claim 224, 225, 226, or 227, wherein X is X' and A' is A'-12.
242. The phenol compound according to claim 224, wherein:
X is X1 A1 isA1-1;
R21 and R22 are both hydrogen; h is 0;
i is an integer of 3 to 5; Z is oxygen;
R2 and R3 are independently chlorine or C1-C3 alkyl; a is 0;
R6 is C1-C5 alkyl, C2-C4 haloalkyl, C3-C6 alkenyl, or C3-C6 haloalkenyl; and
R7 is hydrogen, C1-C4 alkyl, or trifluoromethyl; or wherein:
X is X';
A1 is A1-2;
R21, R22 R23 and R24 are all hydrogen;
h is O;
Q1 is oxygen;
j is 1;
k is an integer of 3 to 6;
Z is oxygen;
R2 and R3 are independently chlorine or C1-C3 alkyl;
a is 0;
R6 is C1-C5 alkyl, C2-C4 haloalkyl, C3-C6 alkenyl, or C3-C6 haloalkenyl;

a is 0;
Z is oxygen;
X is X1
R6 is C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, or C3-C6 haloalkenyl;
A1 is A1-7;
I
G1 is G1-1; al is 0;

W is 1,3-phenylene or 1,4-phenylene;
h and p are both 0; and
^19 1^20^ j^26 j^26^ j^29^ ^^^ R3O ^^^ ^^ hydrogen.
248. The phenol compound according to claim 224, wherein R^ and
R^ are independently halogen or C2-C6 alkyl;
a is 0;
Z is oxygen;
X is X1
R6 is C1-C8 alkyl, C2-C8 haloalkyl, C2-C8 alkenyl, or C3-C6 haloalkenyl;
A1 isA1-8;
G1 is G1-l;
al is 0;
G2 is oxygen;
W is 1,3-phenylene or 1,4-phenylene;
h and p are both 0; and
R19, R2o, R25, R26, R29, and R3O ARE ALL hydrogen.
249. The phenol compound according to claim 224, 225, 226, or
227, wherein X is X2
R8 and R9 are independently hydrogen, C1-C11, alkyl, C1-C6 haloalkyl,
C2-C8 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C8 haloalkynyl, C2-C10
alkoxyalkyl, C2-C10 alkylthioalkyl, or naphthyl,
or C3-C7 cycloalkyl optionally substituted with C1-C4 alkyl,
or C4-C10 cycloalkylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof,
or C2-C8 cycloalkenyl optionally substituted with C1-C4 alkyl,
or C2-C8 cycloalkenylalkyl optionally substituted with C1-C4 alkyl on
the ring thereof,
or T2-l or T2-2 of formula (4)

I
wherein R17, D, R11, R12 b, and d are as defined in claim 224,
or 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, or 3-pyrrolyl, each of which heterocyclic rings may be optionally substituted with one to three identical or different (R18)g's wherein R18 and g are as defined in claim 223,
or R8 and R9 are combined together at their ends to form a saturated or unsaturated 5- or 6-membered ring containing zero to two oxygen or sulfur atoms in the ring.
250. The phenol compound according to claim 224, 225, 226, or

oxygen or sulfur atoms in the ring.
251. The phenol compound according to claim 224, 225, 226, 227,
249, or 250, wherein X is X2 and A2 is A2-l.
252. The phenol compound according to claim 224, 225, 226, 227,
249, or 250, wherein X is X2 and A2 is A2-2.
253. The phenol compound according to claim 224, 225, 226, 227,
249, or 250, wherein X is X2 and A2 is A2-3.
254. The phenol compound according to claim 224, 225, 226, 227,
249, or 250, wherein X is X2 and A2 is A2-A.
255. The phenol compound according to claim 224, 225, 226, 227,
249, or 250, wherein X is X2 and A2 is A2-5.
256. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A'-6.
257. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A='-7 or A'-9.
258. The phenol compound according to claim 224, 225, 226, 227, 249, or 250, wherein X is X2 and A2 is A2-8 or A2-10.
259. The phenol compound according to claim 251, wherein h and p are both 0; and R19 R20, R25 R26 R29 and R30 are all hydrogen.
260. The phenol compound according to claim 252, wherein h and p are both 0; R19 R20, R25 R26 R27, R28, R313, and R32' are all hydrogen; and Q1 is oxygen.
261. The phenol compound according to claim 253, wherein h and p are both 0; R19 R20, R25 R26 R29 R30, R35 and R36 are all hydrogen; and Q2 is oxygen.
262. The phenol compound according to claim 254, wherein h and p are both 0; R19 R20, R25 R26 R29 R30, R35 and R36 are all hydrogen; and Q1 and Q3 are both oxygen.

263. The phenol compound according to claim 255, wherein h and p are both 0; R19 R20 R25 R26 R27 R28 R31, R32 R35 and R36 are all hydrogen; and Q1 and Q2 are both oxygen.
264. The phenol compound according to claim 256, wherein h and p are both 0; R19 R20 R25 R26 R27 R28 R31, R32 R35 and R36 are all hydrogen; and Q1 Q2, and Q3 are all oxygen.
265. The phenol compound according to claim 257, wherein R19 R20 R23, R24, R25, R26, R29, R3o, R35 and R36 ARE ALL hydrogen; and Q1 and Q1 are
both oxygen.
266. The phenol compound according to claim 258, wherein R19
R20 R23 R24 R25 R26 R35 and R36 are all hydrogen; and Q1 and Q2 are both
oxygen.
I ■ '
267. The compound according to claim 224, which is 4-(2,6-dichlo-
ro-4-hydroxyphenoxy)butanal 0-isopropyloxime.
268. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentanal 0-isopropyloxime.
269. The compound according to claim 224, which is 6-(2,6-dichlo-ro-4-hydroxyphenoxy)hexanal 0-isopropyloxime.
270. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butanal 0-tert-butyloxime.
271. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentanal 0-tert-butyloxime.
272. The compound according to claim 224, which is 6-(2,6-dichlo-ro-4-hydroxyphenoxy)hexanal 0-tert-butyloxime.
273. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butanal 0-(2,2,2-trichloroethyl)oxime.
274. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentanal 0-(2,2,2-trichloroethyl)oxime.

275. The compound according to claim 224, which is 6-(2,6-dichlo-ro-4-hydroxyphenoxy)hexanal 0-(2,2,2-trichloroethyl)oxime.
276. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butanal 0-(3,3-dichloro-2-propenyl)oxime.
277. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentanal 0-(3,3-dichloro-2-propenyl)oxime.
278. The compound according to claim 224, which is 6-(2,6-dichlo-ro-4-hydroxyphenoxy)hexanal 0-(3,3-dichloro-2-propenyl)oxime.
279. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-isopropyloxime.
280. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-isopropyloxime.
281. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetone 0-isopropyloxime.
282. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetone 0-isopropyloxime.
283. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-tert-butyloxime.
284. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-tert-butyloxime.
285. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxy|)henoxy)butyloxyacetone 0-tert-butyloxime.
286. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetone 0-tert-butyloxime.
287. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime.
288. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-(2,2,2-trichloroethyl)oxime.

289. The compound according to claim 224, which is 4-(2,6-dichlo ro-4-hydroxyphenoxy)butyloxyacetone 0-(2,2,2-trichloroethyl)oxime.
290. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetone 0-(2,2,2-trichloroethyl)oxime.
291. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)-oxime.
292. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetaldehyde 0-(3,3-dichloro-2-propenyl)-oxime.
293. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)butyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime.
294. The compound according to claim 224, which is 5-(2,6-dichlo-ro-4-hydroxyphenoxy)pentyloxyacetone 0-(3,3-dichloro-2-propenyl)oxime.
295. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)methylbenzaldehyde 0-sec-butyloxime.
296. The compound according to claim 224, which is 4-(2,6-dichlo-ro-4-hydroxyphenoxy)methylbenzaldehyde 0-t-butyloxime.
297. The compound according to claim 224, which is 4-(2-(2,6-di-chloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-sec-butyloxime.
298. The compound according to claim 224, which is 4-(2-(2,6-di-chloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-allyloxime.
299. The compound according to claim 224, which is 4-(2-(2,6-di-chloro-4-hydroxyphenoxy)ethyl)benzaldehyde 0-(3,3-dichloro-2-propenyl)-oxime.
r I I
300. The compound according to claim 224, which is 4-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-n-propyloxime.
301. The compound according to claim 224, which is 4-(3-(2,6-di-

chloro-4-hydroxyphenoxy)propyloxy)benzaldehydeO-isopropyloxime.
302. The compound according to claim 224, which is 4-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)benzaldehydeO-sec-butyloxime.
303. The compound according to claim 224, which is 4-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)benzaldehyde 0-t-butyloxime.
304. The compound according to claim 224, which is 4'-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)acetophenone 0-ethyloxime.
305. The compound according to claim 224, which is 4'-(3-(2,6-di-chloro-4-hydroxyphenoxy)propyloxy)propiophenone 0-ethyloxime.
306. The compound according to claim 224, which is 4'-(4-(2,6-di-chloro-4-hydroxyphenoxy)butyloxy)acetophenone 0-ethyloxime.
307. The compound according to claim 224, which is 4'-(4-(2,6-di-chloro-4-hydroxyphenoxy)butyloxy)acetophenone 0-n-propyloxime.
308. The compound according to claim 224, which is 4-(4'(2,6-di-chloro-4-hydroxyphenoxy)butyloxy)benzaldehyde 0-isopropyloxime.
309. The compound according to claim 224, which is 4'-(3-(2,6-di-
chloro-4-hydroxyphenoxy)propyloxy)-2,2,2-trifluoroacetophenone 0-ethyloxime.
310. The compound according to claim 224, which is 4-(trifluoro-methyl)benzaldehyde 0-(4-(2,6-dichloro-4-hydroxyphenoxy)butyl)oxime.
311. The compound according to claim 224, which is 4'-(trifluoro-methyl)acetophenone 0-(4-(2,6-dichloro-4-hydroxyphenoxy)butyl)oxime.
312. The compound according to claim 224, which is trimethyl-acetaldehyde 0-(5-(2,6-dichloro-4-hydroxyphenoxy)pentyl)oxime.
313. The compound according to claim 224, which is 3,3-dimethyl-2-butanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)pentyl)oxime.
314. The compound according to claim 224, which is 3,3-dimethyl-2-butanone 0-(4-(2,6-dichloro-4-hydroxyphenoxy)butyl)oxime.

, ' ■ ■
1 , I
315. The compound according to claim 224, which is 4-methyI-2-
pentanone 0-(4-(2,6-dichloro-4-hydroxyphenoxy)butyl)oxime.
316. The compound according to claim 224, which is 4-methyl-2-
pentanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)pentyl)oxime.
317. The compound according to claim 224, which is 3-methyl-2-
4
butanone 0-(5-(2,6-dichloro-4-hydroxyphenoxy)pentyl)oxime.
318. A compound of formula (51)
wherein:
R57is C1-C8 alkyl, C2-C6 haloalkyl, C3-C6 alkenyl, C3-C6 haloalkenyl,
C3-C6 alkynyl, C3-C6 haloalkynyl, or triphenylmethyl,
or C3-C7 cycloalkyl, optionally substituted C1-C4 alkyl,
or C4-C10 cycloalkylalkyl, optionally substituted C1-C4 alkyl on the
ring thereof,
or C3-C6 cycloalkenyl, optionally substituted C1-C4 alkyl,
or C3-C6 cycloalkenylalkyl, optionally substituted C1-C4 alkyl on the
ring thereof,

tuents selected from halogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 halo-alkynyl, C1-C6 alkoxy, C1-C3 haloalkoxy, C2-C6 alkenyloxy, C2-C6 haloalkenyloxy, C2-C6 alkynyloxy, C2-C6 haloalkynyloxy, (C1-C5 alkoxy)carbonyl, cyano, or nitro;
R11, R12, R13, and R14 are independently hydrogen, C1-C3 alkyl, or trifluoromethyl;
D is -CH= or nitrogen;
b is an integer of 0 to 5;
d is an integer of 1 to 3;
e is an integer of 0 to 3;
f is an integer of 2 to 4;
R7 is hydrogen, C1-C6 alkyl, C1-C3 haloalkyl, C2-C6 cycloalkyl, cyano, cyano C1-C3 alkyl, (C1-C4 alkoxy)carbonyl, or (C1-C4 alkoxy)carbonyl(C1-C3)alkyl,
or phenyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy,
or benzyl optionally substituted with halogen, C1-C4 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, or C1-C3 haloalkoxy on the ring thereof;
R58 is hydrogen or C1-C4 alkyl;
R59 is hydrogen or C1-C4 alkyl;
or R59 and R7 may be combined together at their ends to form trimethylene, tetramethylene, or pentamethylene, each of which may be optionally substituted with C1-C3 alkyl;
L7 is hydroxy, chlorine, bromine, iodine, mesyloxy, or tosyloxy; and
G4 is G4.2, G4-3, or G4-4 of formula (53)

G4-2: -(CR60R61)k-
G4-4:-(CR60R61)M-C = C-(CR62R63)N-wherein:
R60, R61 R62 R63 R64, and R65 ARE independently
hydrogen or C1-C3 alkyl;
k is an integer of 2 or 8;
m is an integer of 1 to 3; and
n is an integer of 1 to 3.
319. An oxime compound, substantially as herein described, and exempli f ied.
3 20. A phenol compound, substantially as herein described, and exemplified.

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Patent Number

209075

Indian Patent Application Number

715/MAS/1998

PG Journal Number

13/2008

Publication Date

31-Mar-2008

Grant Date

20-Aug-2007

Date of Filing

03-Apr-1998

Name of Patentee

M/S. SUMITOMO CHEMICAL COMPANY LIMITED

Applicant Address

5-33, KITAHAMA 4-CHOME, CHUO-KU, OSAKA 541-8550

Inventors:

#	Inventor's Name	Inventor's Address
1	KEIICHI IZUMI	2-10-1 154 SONCHIGASHI-MACHI, TOYONAKA-SHI, OSAKA-FU
2	NORIYASU SAKAMOTO	2-10-2-232 SONEHIGASHI-MACHI, TOYONAKA-SHI, OSAKA-FU,
3	SHIGERU SAITO	2-11-8-108 OF SONEHIGASHI-MACHI, TOYONAKA-SHI, OSAKA-FU
4	HIROSHI IKEGAMI	2-14-7, MEFU, TAKARAZUKA-SHI, HYOGO-KEN
5	MASAYA SUZUKI	2-14-7, MEFU, TAKARAZUKA-SHI, HYOGO-KEN

PCT International Classification Number

C07C 251/32

PCT International Application Number

N/A

PCT International Filing date

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	089831/1997	1997-04-08	Japan
2	245892/1997	1997-08-06	Japan
3	247400/1997	1997-08-07	Japan