Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D213/86—Hydrazides; Thio or imino analogues thereof
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
  • A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
  • A01N37/28—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
  • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
  • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
  • A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
  • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
  • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
  • A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
  • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
  • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
  • A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
  • A01N43/38—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
  • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
  • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
  • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
  • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
  • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
  • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
  • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
  • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

• Hydrazone derivatives for combatting harmful insects and arachnids Hydrazone derivatives for combatting harmful insects and arachnids
• the present invention relates to a method for combating harmful insects and arachnids.
• WO 87/66133 describes acyl hydrazones which are useful for killing internal parasites, such as nematodes, trematodes and cestodes, affecting warm-blooded animals and humans.
• US 3066023 discloses aroylhydrazones as components of a photoconducting insulating layer in a material for xerography.
• WO 99/01423 discloses the preparation of aroylhydrazones which are useful as gluca- gon antagonists or inverse agonists.
• EP-A 322691 discloses aroylhydrazones as precursors for the preparation of 1- acylpyrazolines.
• Ar is a cyclic radical selected from phenyl, naphthyl and a 5- or 6-membered heterocyclic radical with 1 to 4 heteroatoms which are selected, independently of one another, from O, N and S, where the 5- or 6-membered heterocyclic radical may be fused to 1 or 2 phenyl rings, and where the cyclic radical may have 1 , 2, 3, 4 or 5 substituents R a which are selected, independently of one another, from halogen, cyano, nitro, C C 10 -alkyl, C C 10 -haloalkyl, C 3 -C 10 -cylcoalkyl, C 3 -C 10 - halocycloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 - haloalkynyl, CrC 10 -alkoxy, d-Cio-
• R b which are selected, independently of one another, from halogen, cyano, nitro, C C ⁇ o-alkyl, C C 10 -haloalkyl, C 3 -C 10 - cylcoalkyl, C 3 -C 10 -halocycloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 - alkynyl, C 3 -C 10 -haloalkynyl, d-do-alkoxy, d-do-haloalkoxy, C 2 -C 10 -alkenyloxy,
• X is CO or SO 2 ;
• R 1 is H, Ci-Cio-alkyl, CrC 10 -haloalkyl, C 3 -C 10 -cycloalkyl, C 3 -C ⁇ 0 -halocycloalkyl, C 2 - C 10 -alkenyl, C 2 -C ⁇ o-haloalkenyl, C 2 -C 10 -alkynyl, C 2 -C 10 -haloalkynyl or phenyl which may be substituted by 1 to 5 substituents which are selected, independently of one another, from halogen, cyano, nitro, CrC 10 -alkyl, d-Cio-haloalkyl, C 3 -C ⁇ o-cylcoalkyl, C 3 -C 10 -halocycloalkyl, C 2 -C 10 -alkenyl, C 2 -C ⁇ 0 -haloalkenyl, C 2 - C ⁇ o-alkynyl, C 3
• R 2 and R 3 are independently of one another H, halogen, cyano, d-do-alkyl, C C 10 - haloalkyl, C 3 -C 10 -cylcoalkyl, C 3 -C 10 -halocycloalkyl, C 2 -C 10 -alkenyl, C 2 -C ⁇ o- haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 -haloalkynyl, d-Cio-alkoxy, d-Cio-haloalkoxy,
• R 4 is an aromatic radical selected from phenyl, pyridyl, pyrimidyl or furyl, thienyl, where the aromatic radical may carry 1 , 2, 3, 4 or 5 substituents R c which are selected, independently of one another, from halogen, cyano, nitro, d-do-alkyl, C Cio-haloalkyl, C 3 -C 10 -cylcoalkyl, C 3 -C 10 -halocycIoalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 - haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 -haloalkynyl, CrC 10 -alkoxy, C C 10 -haloalkoxy, d-do-alkenyloxy, C 2 -C 10 -haloalkenyloxy, C 2 -C ⁇ 0 -alkynyloxy
• R 5 R 6 N-CO- and phenoxy which may be substituted by 1 , 2, 3, 4 or 5 substituents R d which are selected, independently of one another, from halogen, cyano, nitro, d-Cio-alkyl, d-do-haloalkyl, C 3 -C 10 -cylcoalkyl, C 3 -C 10 -halocycloalkyl, C 2 -C 10 - alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 -haloalkynyl, CrC 10 -alkoxy, C r do-haloalkoxy, C 2 -C 10 -alkenyloxy, C 2 -C 10 -haloalkenyloxy, C 2 -C 10 -alkynyloxy, C 3 -
• R 2 and R 4 together with the carbon atoms to which they are bound form a phenyl ring or a 5- or 6-membered heterocyclic ring with 1 or 2 heteroatoms which are selected, independently of one another, from O, N and S, where the phenyl ring and the 5- or 6-membered heterocyclic ring may be fused to a phenyl ring, and where the phenyl ring and the 5- or 6-membered heterocyclic ring and/or the phenyl ring to which they are fused may carry 1 , 2, 3 or 4 substituents R e , which are selected, independently of one another, from halogen, cyano, nitro, C C ⁇ o- alkyl, C C 10 -haloalkyl, C 3 -C 10 -cylcoalkyl, C 3 -C 10 -halocycloalkyl, C 2 -C 10 -alkenyl, C 2 -do-haloalkenyl, C
• R 5 and R 6 independently of one another are H or d-do-alkyl
• n O or l
• the present invention therefore relates to a method for combating harmful insects and arachnids, which comprises contacting the insects or the arachnids, their habitat, breeding ground, food supply, plant, seed, soil, area, material or environment in which the insects or arachnids grow or may grow, or the materials, plants, seeds, soil, surfaces or spaces to be protected against attack or infestation by insects or arachnids with a pesticidally effective amount of a hydrazone compound of the formula I.
• the invention especially relates to a method for protecting crops from attack or infestation by insects or arachnids, which comprises contacting a crop with a pesticidally effective amount of a compound of the formula I as defined above.
• Suitable compounds of the general formula I encompass all possible stereoisomers (cis/trans isomers) which may occur and mixtures thereof.
• Suitable compounds also encompass possible enantiomers and racemic mixtures.
• Salts of the compounds of the formula I which are suitable for the use according to the invention are especially agriculturally acceptable salts. They can be formed in a customary method, e.g. by reacting the compound with an acid of the anion in question.
• Suitable salts include adducts of compounds I with maleic acid, dimaleic acid, fumaric acid, difumaric acid, methane sulfenic acid, methane sulfonic acid, and succinic acid.
• salts include those that can form with, for example, amines, metals, alkaline earth metal bases or quaternary ammonium bases, including zwitterions.
• Suitable metal and alkaline earth metal hydroxides as salt formers include the salts of barium, aluminum, nickel, copper, manganese, cobalt zinc, iron, silver, lithium, sodium, potassium, magnesium or calcium.
• Additional salt formers include chloride, sulfate, acetate, carbonate, hydride, and hydroxide.
• Desirable salts include adducts of compounds I with maleic acid, dimaleic acid, fumaric acid, difumaric acid, and methane sulfonic acid.
• the term "5- or 6-membered heterocyclic radical with 1 to 4 heteroatoms which are selected, independently of one another, from O, N and S" as used herein refers to both aromatic and non-aromatic rings such as saturated or partially unsaturated radicals having from 1 to 4, preferably 1 ,2, or 3 heteroatoms as ring members.
• heteroaromatic rings examples include triazinyl, pyrazinyl, pyrimidyl, pyridazinyl, pyridyl, thienyl, furyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl, thiazolyl, oxazolyl, thiadiazolyl, oxadiazolyl, isothiazolyl or isoxazolyl.
• the 5- or 6-membered heteroaromatic ring is fused to 1 or 2 phenyl rings, this refers e.g. to quinolinyl, isoquinolinyl, indolyl, indolizinyl, isoindolyl, indazolyl, benzofuryl, benzthienyl, benzthiazolyl, benzoxazolyl, benzimidazolyl, dibenzopyrrolyl, dibenzofu- ranyl or dibenzothienyl.
• non-aromatic rings are pyrrolidinyl, pyrazolinyl, imidazolinyl, pyrrolinyl, pyrazolinyl, imidazolinyl, tetrahydrofuranyl, dihydrofuranyl, dioxolanyl, dioxolenyl, thiolanyl, dihydrothiophenyl, oxazolidinyl, isoxazolidinyl, oxazolinyl, isoxazolinyl, thia- zolinyl, isothiazolinyl, thiazolidinyl, isothiazolidinyl, oxathiolanyl, piperidinyl, piperazinyl, pyranyl, dihydropyranyl, tetrahydropyranyl, dioxanyl, thiopyranyl, dihydrothiopyranyl, tetrahydrothiopyranyl,
• the 5- or 6-membered heterocyclic non-aromatic radical is fused to a phenyl group, this refers to e. g. dihydroindolyl, dihydroindolizinyl, dihydroisoindolyl, dihydrochinolinyl, dihydroisochinolinyl, chromenyl, chromanyl and the like.
• 5- or 6-membered heterocyclic ring with 1 or 2 heteroatoms which are selected, independently of one another, from O, N and S, where the 5- or 6-membered heterocyclic ring may be fused to a phenyl ring refers e.g.
• the 5- or 6-membered heterocyclic ring with 1 or 2 heteroatoms which may be fused to a phenyl ring contains a carbonyl group as a ring member, this refers to e. g. pyrroli- donyl, pyrazolidonyl, pyrazolonyl, oxazolidonyl, pyridonyl, pyronyl, indoxylyl, oxindolyl, cumarinyl, chromenonyl (chromonyl) and the like.
• Halogen will be taken to mean fluoro, chloro, bromo and iodo.
• d-do-alkyl refers to a branched or unbranched saturated hydrocarbon group having 1 to 10 carbon atoms, for example methyl, ethyl, propyl, 1- methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1- methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1- dimethylpropyl, 1 ,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4- methylpentyl, 1,1-dimethylbutyl, 1 ,2-dimethylbutyI, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbuty
• d-C ⁇ 0 -haloalkyl refers to a straight-chain or branched alkyl group having 1 to 10 carbon atoms (as mentioned above), where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above, for example d-C 4 -haloalkyl, such as chloromethyl, bromomethyl, dichloro- methyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2- fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2- difluoroethyl, 2,2-dichloro
• C C 10 -alkoxy and “d-Cio-alkylthio” refer to straight-chain or branched alkyl groups having 1 to 10 carbon atoms (as mentioned above) bonded through oxygen or sulfur linkages, respectively, at any bond in the alkyl group.
• Examples include d-C 4 - alkoxy such as methoxy, ethoxy, propoxy, isopropoxy, butoxy, sec-butoxy, isobutoxy and tert-butoxy, futher d-C 4 -alkylthio such as methylthio, ethylthio, propylthio, isopropylthio, and n-butylthio.
• C C 10 -haloalkoxy and " C r C 10 -haloalkylthio” refer to straight- chain or branched alkyl groups having 1 to 10 carbon atoms (as mentioned above) bonded through oxygen or sulfur linkages, respectively, at any bond in the alkyl group, where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above, for example C C 2 -haloalkoxy, such as chloromethoxy, bromomethoxy, dichloromethoxy, trichloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorofluoromethoxy, dichlorofluoromethoxy, chlorodifluoromethoxy, 1-chloroethoxy, 1-bromoethoxy, 1-fluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro
• C 2 -C ⁇ 0 -alkenyl intends a branched or unbranched unsaturated hydrocarbon group having 2 to 10 carbon atoms and a double bond in any position, such as ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3- butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2- propenyl; 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl- 1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl
• C 2 -C 10 -haloalkenyl intends a branched or unbranched unsaturated hydrocarbon group having 2 to 10 carbon atoms and a double bond in any position, where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above.
• C 2 -d 0 -alkenyloxy intends a branched or unbranched unsaturated hydrocarbon group having 2 to 10 carbon atoms and a double bond in any position, the alkenyl group being bonded through oxygen linkages, respectively, at any bond in the alkenyl group, for example ethenyloxy, propenyloxy and the like.
• C 2 -C 10 -haloalkenyloxy intends a branched or unbranched unsaturated hydrocarbon group having 2 to 10 carbon atoms and a double bond in any position, the alkenyl group being bonded through oxygen linkages, respectively, at any bond in the alkenyl group, where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above.
• C 2 -C 10 -alkynyl refers to a branched or unbranched unsaturated hydrocarbon group having 2 to 10 carbon atoms and containing at least one triple bond, such as ethynyl, propynyl, 1-butynyl, 2-butynyl, and the like.
• C 3 -C 10 -haloalkynyl refers to a branched or unbranched un- saturated hydrocarbon group having 3 to 10 carbon atoms and containing at least one triple bond, where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above, with the proviso that the halogen atom is not directly bound to the triple bond.
• C 2 -C 10 -alkynyloxy refers to a branched or unbranched unsaturated hydrocarbon group having 2 to 10 carbon atoms and containing at least one triple bond, the alkynyl group being bonded through oxygen linkages at any bond in the alkynyl group.
• C 3 -C 10 -haloalkynyloxy refers to a branched or unbranched unsaturated hydrocarbon group having 3 to 10 carbon atoms and containing at least one triple bond, the group being bonded through oxygen linkages at any bond in the alkynyl group, where some or all of the hydrogen atoms in these group may be replaced by halogen atoms as mentioned above, with the proviso that the halogen atom is not directly bound to the triple bond.
• C 3 -C 10 -cycloalkyl refers to a monocyclic 3- to 10-membered saturated carbon atom ring, e.g. cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclo- heptyl, cyclooctyl and cyclodecyl.
• C 3 -C 10 -halocycloalkyl refers to a monocyclic 3- to 10- membered saturated carbon atom ring, e.g. cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl and cyclodecyl, where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above, for example chloro-, dichloro- and trichlorocyclopropyl, fluoro-, difluoro- and trifluorocyclopropyl, chloro-, dichloro-, trichloro, tetrachloro-, pentachloro- and hexachlorocyclohexyl and the like.
• Ar is a cyclic radical selected from phenyl, naphthyl, a 5- or 6-membered heterocyclic radical with 1 to 3 heteroatoms which are selected, independently of one another, from O, N and S, where the 5- or 6-membered heterocyclic radical may be fused to 1 or 2 phenyl rings and where the cyclic radical is unsubstituted or substituted as defined above, i.e. by 1, 2, 3, 4 or 5 of the above mentioned radicals R a .
• Ar is a cyclic radical selected from phenyl, triazinyl, pyrazinyl, pyrimidyl, pyridazinyl, pyridyl, thienyl, furyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, thiazolyl, oxazolyl, thiadiazolyl, oxadiazolyl, isothiazolyl, isoxazolyl, naphthyl, quinolinyl, isoquinolinyl, indolyl, indazolyl, benzofuryl, benzthienyl, benzthiazolyl, benzoxazolyl, benzimidazolyl, chromenyl, chromenonyl, dibenzopyranyl or fluorenyl and where the cyclic radical is unsubstituted or substituted as defined above.
• Ar is a cyclic radical selected from phenyl, tri
• Ar is a cyclic radical selected from thienyl, furyl, pyrrolyl, pyrazolyl, imidazolyl, tria- zolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, phenyl, pyridyl, pyrazinyl, pyrimidyl, pyridazinyl, naphthyl, dibenzopyranyl, indolyl, benzimidazolyl, benzofuryl, benzoxazolyl, benzothienyl, benzthiazolyl or chrome- nonyl and where the cyclic radical is unsubstituted or substituted by 1 , 2, 3, 4 or 5 of the above mentioned radicals R a .
• Ar is a cyclic radical selected from thienyl, furyl, pyrazolyl, imidazolyl, isoxazolyl, thiazolyl, thiadiazolyl, phenyl, pyridyl, pyrazinyl, naphthyl, dibenzopyranyl, indolyl or benzothieny and where the cyclic radical is unsubstituted or substituted by 1 , 2, 3, 4 or 5 of the above mentioned radicals R a .
• Ar is a cyclic radical selected from thienyl, furyl, pyrazolyl, imidazolyl, isoxazolyl, phenyl, pyridyl, pyrazinyl, naphthyl, indolyl or benzothienyl, especially thienyl, furyl, pyrazolyl, imidazolyl, isoxazolyl, phenyl, pyridyl, pyrazinyl, naphthyl or indo- lyl and where the cyclic radical is unsubstituted or substituted by 1 , 2, 3, 4 or 5 of the above mentioned radicals R a .
• Ar is a cyclic radical selected from thienyl, furyl, pyrazolyl, phenyl, isoxazolyl or pyridyl and where the cyclic radical is unsubstituted or substituted by 1 , 2, 3, 4 or
• the cyclic radical mentioned for Ar is unsubstituted or carries 1 , 2, 3 or 4 substituents R a , in particular 1 , 2 or 3 and more preferably 1 or 2 substituents R a .
• Preferred substituents R a are selected, independently of one another, from halogen, cyano, nitro, Ci-Cio-alkyl, d-do-haloaikyl, C 3 -C 10 -cylcoalkyl, C 3 -C 10 -halocycloalkyl, C do-alkoxy, d-Cio-haloalkoxy, C C 10 -alkylthio, C C 10 -haloalkylthio, d-C 10 - alkylsulfonyl, d-C 10 -haloalkylsulfonyl, hydroxy, phenyl, phenoxy, NR 5 R 6 , d-do- alkoxycarbonyl, CrC 10 -haIoalkoxycarbonyl, CrC 10 -alkylcarbonyl, C r C 10 - haloalkylcarbonyl and NR 5 R 6 -CO-.
• substituents R a are selected, independently of one another, from halogen, hydroxy, d-C 4 -alkyl, C C -haloalkyl, d-C 4 -alkoxy, C C 4 -haloalkoxy, phenyl, which is unsubstituted or substituted by by 1 to 3 substituents R b which are in particular selected, independently of one another, from halogen, C C 4 -alkyl, C C 4 -haloalkyl and d-C 4 -alkoxy, especially by halogen, and phenoxy which is unsubstituted or substituted by 1 to 3 substituents R which are in particular selected, independently of one another, from halogen, CrC 4 -alkyl, C C 4 -haloalkyl and C C 4 -alkoxy, especially by C C 4 - haloalkyl.
• R a are selected, independently of one another, from halogen, C C 4 -alkyl, CrC 4 -haloalkyl, C r C 4 -alkoxy and C C 4 -haloalkoxy.
• substituents R a are selected, independently of one another, from fluorine, chlorine, bromine, C C 4 -alkyl, C C 4 -alkoxy, in particular methoxy, C C 4 - haloalkoxy, in particular difluoromethoxy or trifluoromethoxy and CF 3 .
• R 2 is H, d-Cio-alkyl, d-do-haloalkyl, halogen, phenyl or cyano.
• R 2 is H, C C 10 -alkyl, , in particular C C 4 -alkyl, halogen, phenyl or cyano.
• R 2 is H, d-do-alkyl, in particular C C 4 -alkyl or halogen, e.g. methyl, ethyl, isopro- pyl, fluorine, chlorine or bromine.
• R 2 is C C -alkyl, in particular methyl or ethyl.
• R 3 is H, d-C 4 -alkyl, d-C -haloalkyl, halogen or phenyl.
• R 3 is H, d-C 4 -alkyl, halogen or phenyl, especially H or halogen.
• R 4 is an aromatic radical selected from phenyl, pyridyl, pyrimidyl, furanyl, thienyl or benzofuryl where the aromatic radical is unsubstituted or substituted as defined above, i.e. by 1 , 2, 3, 4 or 5 of the above mentioned radicals R G .
• the aromatic radical as mentioned for R 4 may be unsubstituted or may carry 1 to 5, preferably 1 to 4, more preferably 1 to 3 and in particular 1 or 2 substituents R c .
• Preferred substituents R c are selected, independently of one another, from hydroxy, halogen, cyano, nitro, C ⁇ -C 10 -alkyl, C r C 10 -haloalkyl, C 3 -C 10 -cylcoalkyl, C 3 -C 10 - halocycloalkyl, C C 10 -alkoxy, d-Cio-haloalkoxy, d-do-alkylthio, d-Cio-haloalkylthio, d-do-alkylsulfonyl, C C 10 -haloalkylsulfonyl, NR 5 R 6 , C C 10 -alkoxycarbonyl, C C 10 - haloalkoxycarbonyl, R
• substituents R G are selected, independently of one another, from halogen, d-C 4 -alkyl, C C 4 -haloalkyl, C C 4 -alkoxy, d-d-haloalkoxy, C C 4 -alkylthio, d-C 4 -haloalkylthio, cyano, nitro, NR 5 R 6 and phenoxy which may be substituted by d- C -haloalkyl.
• R c are selected, independently of one another, from halogen, d-C -alkyl, C C 4 -haloalkyl, d-C 4 -alkoxy, C C -haloalkoxy and C C 4 - haloalkylthio, e.g. from fluorine, chlorine, methyl, ethyl, propyl, isopropyl, butyl, fluoro- methyl, difluoromethyl, trifluoromethyl, methoxy, difluoromethoxy, trifluoromethoxy and trifluoromethylthio.
• R c are selected, independently of one another, from halogen, C C 4 -alkyl and d-C 4 -haloalkyl.
• R 4 is phenyl, which carries 1 , 2 or 3 of the aforementioned substituents R c , then at least one of the substituents is preferably located in the 2, 4 and/or 6-postion.
• Examples of paricularly preferred substituted phenyl are those mentioned in tables 2 and 3 as radicals R 4 .
• R 2 and R 4 together with the carbon atoms to which they are bound form a phenyl ring or a 5- or 6-membered heterocyclic ring with 1 or 2 heteroatoms which are selected, independently of one another, from O, N and S, where the 5- or 6-membered heterocyclic ring may be fused to a phenyl ring, and where the 5- or 6-membered heterocyclic ring and/or the phenyl ring to which it is fused may carry 1 , 2, 3 or 4 of the aforementioned substituents R e .
• the substituents R e are selected, independently of one another, from halogen, d-C 4 -alkyl, C r C -haloalkyl, d-C 4 -alkoxy, d-C 4 - haloalkoxy, C C 4 -alkylthio, C r C 4 -haloalkylthio, cyano, nitro, phenyl, which is unsubstituted or is substituted by 1 , 2 or 3 substituents R f which are selected, independently of one another, from C r C 4 -alkyl, C C 4 -haloalklyl C C -alkoxy and halogen, and phenoxy which is unsubstituted or substituted by 1 to 3 substituents which are selected, independently of one another, from d-C 4 -alkyl, C r C 4 -haloalklyl, d-C 4 -alkoxy and halogen, and where the 5-
• R 3 is either H or is one of the above-mentioned substituents of the moiety formed by R 2 and R 4 together with the carbon atoms to which they are bound.
• substituents R e are selected, independently of one another, from halogen, d-C 4 -alkyl, d-C 4 -haloalkyl, C C 4 -haloalkoxy, d-C 4 -haloalkylthio, cyano, nitro, phenyl, which is unsubstituted or is substituted by 1 , 2 or 3 substituents which are selected, independently of one another, from d-C 4 -haloalklyl and halogen, and phenoxy which is unsubstituted or substituted by d-C 4 -haloalklyI.
• the substituents R e are selected, independently of one another, from halogen, C C 4 -alkyl, C C 4 -haloalkyl, d- C 4 -alkoxy, d-C 4 -haloalkoxy, C C 4 -haloalkylthio, cyano and nitro. More preferably substituents R e are selected, independently of one another, from C C 4 -alkyl, C ⁇ -C 4 - haloalkyl and halogen.
• radicals R b , R d and R f are selected from halogen, C C 4 -alkyl, C C 4 -haloalkyl, d-C 4 -haloalkoxy, CrC 4 -haloalkylthio, cyano and nitro, especially from halogen, C ⁇ -C 4 -alkyl, d-C 4 -alkoxy, d-C 4 -haloalkyl, C C 4 -haloalkoxy.
• R a , R 1 and R 3 are as defined herein,
• n 0, 1, 2 or 3
• R 2a is H or d-C 4 alkyl
• R 4a is phenyl, which may carry 1 , 2, 3 or 4 substituents R c as defined herein,
• R 2a is C C 4 alkyl and additionally one of the following provisions i) to iv) are met, the compounds la are new and thus are part of the present invention: i) m is not 0 or ii) R 4a carries at least one substituent R G being different from hydrogen iii) or R 1 is different from hydrogen, iv) or R 2a is different from methyl.
• R a in formula la has one of the meanings which are indicated as being preferred, more preferred, particularly preferred or especially preferred.
• R a is Halogen, in particular F, CI or Br, d-d-alkyl, in particular methyl or ethyl, phenyl, difluoromethyl, trifluoromethyl or d-C 4 -alkoxy, in particular methoxy.
• R 1 and R 3 have, independently of each other, one of the meanings which are indicated as being preferred, more preferred, particularly preferred or especially preferred. Most preferred are compounds la, wherein R 1 and R 3 are hydrogen.
• the substituent R c has one of the meanings which are indicated as being preferred, more preferred, particularly preferred or especially preferred.
• R c is selected from F, CI, methoxy or methyl.
• substituted phenyl is selected from one of the meanings given for R 4 in tables 3 or 4, in particular from 2- fluorophenyl, 3-fluorophenyl, 4-fluorophenyl, 2,4-difluorophenyl, 3,4-difluorophenyl, 3,5- difluorophenyl, 2,6-difluorophenyl, 2,4,6-trifluorophenyl, 2-chlorophenyl, 3-chlorophenyl, 3,5-dichlorophenyl, 2,6-dichlorophenyl, 4-chlorophenyl, 2-fluoro-4-chlorophenyl, 3- fluoro-4-trifluoromethylphenyl, 3,4,5-trifluorophenyl, 2-triflu
• R is most preferably methyl or ethyl.
• n, X, R ⁇ R 2 , R 3 and R 4 are as defined herein, and
• Ar is isoxazolyl, which may carry 1 or 2 substituents R a as defined herein.
• Ar does not carry an optionally substituted phenyl group as a radical R a if Ar is substituted 4-isoxazolyl these compounds are new and are also part of the present invention.
• n, X, R a , R 1 , R 2 , R 3 and R 4 have, independently of each other, one of the meanings which are indicated as being preferred, more preferred, particularly preferred or especially preferred.
• the variables R 1 , R 2 , R 3 and R a have the meanings outlined below:
• R 1 is H
• R 2 is H or d-C 4 alkyl most preferably methyl or ethyl
• R 3 is H
• R 4 is phenyl, which may carry 1 , 2, 3 or 4 substituents R c as defined herein,
• the substituent R c has one of the meanings which are indicated as being preferred, more preferred, particularly preferred or especially preferred.
• R c is selected from F, CI, methoxy or methyl.
• substituted phenyl is selected from one of the meanings given for R 4 in tables 3 or 4, in particular from 2- fluorophenyl, 3-fluorophenyl, 4-fluorophenyl, 2,4-difluorophenyl, 3,4-difluorophenyl, 3,5- difluorophenyl, 2,6-difluorophenyl, 2,4,6-trifluorophenyl, 2-chlorophenyl, 3-chlorophenyl, 3,5-dichlorophenyl, 2,6-dichlorophenyl, 4-chlorophenyl, 2-fluoro-4-chlorophenyl, 3- fluoro-4-trifluoromethylphenyl, 3,4,5-trifluorophenyl, 2-triflu
• n, X, R 1 , R 2 , R 3 and R 4 are as defined in claim 1 ,
• Ar is pyrazolyl which carries a substituent R a2 on the pyrazol nitrogen atom, and which may additionally carry 1 or 2 substituents R a as defined in claim 1 , wherein R a2 is selected from d-Cio-alkyl, C C ⁇ o-haloalkyl, C 3 -C 10 -cylcoalkyl, C 3 -C 10 - halocycloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 - haloalkynyl, phenyl and benzyl, wherein phenyl and benzyl may be unsubstituted or substituted by 1 , 2, 3, 4 or 5 substituents R b as defined in claim 1
• n, X, R a , R b , R 1 , R 2 , R 3 and R 4 have, independently of each other, one of the meanings which are indi- cated as being preferred, more preferred, particularly preferred or especially preferred.
• R a2 is preferably selected from d-C 6 -alkyl, C 3 -C 6 -cycloalkyl or phenyl. In a particularly preferred embodiment R a2 is d-C 4 -alkyl.
• R 1 is H
• R 2 is H or C ⁇ -C 4 alkyl most preferably methyl or ethyl
• R 3 is H, and R 4 is phenyl, which may carry 1 , 2, 3 or 4 substituents R c as defined herein,
• the substituent R° has one of the meanings which are indicated as being preferred, more preferred, particularly preferred or especially preferred.
• R c is selected from F, CI, methoxy or methyl.
• substituted phenyl is selected from one of the meanings given for R 4 in tables 3 or 4, in particular from 2- fluorophenyl, 3-fluorophenyl, 4-fluorophenyl, 2,4-difluorophenyl, 3,4-difluorophenyl, 3,5- difluorophenyl, 2,6-difluorophenyl, 2,4,6-trifluorophenyl, 2-chlorophenyl, 3-chlorophenyl, 3,5-dichlorophenyl, 2,6-dichlorophenyl, 4-chlorophenyl, 2-fluoro-4-chlorophenyl, 3- fluoro-4-trifluoromethylphenyl, 3,4,5-trifluorophenyl, 2-trifluorome
• R a , R 1 and R 3 are as defined herein,
• n 1 , 2 or 3
• R 2d is H or C C 4 alkyl
• R 4d is phenyl, which may carry 1 , 2, 3 or 4 substituents R G as defined herein,
• R a in formula Id has one of the meanings which are indicated as being preferred, more preferred, particularly preferred or especially preferred.
• R a is Halogen, in particular F, CI or Br, d-C 4 -alkyl, in particular methyl or ethyl, phenyl, difluoromethyl, trifluoromethyl or d-C -alkoxy, in particular methoxy.
• R a is halogen, especially fluorine.
• R 1 and R 3 have, independently of each other, one of the meanings which are indicated as being preferred, more preferred, particularly preferred or especially preferred. Most preferred are compounds la, wherein R 1 and R 3 are hydrogen.
• the substituent R c has one of the meanings which are indicated as being preferred, more preferred, particularly preferred or especially preferred.
• R c is selected from F, CI, methoxy or methyl.
• substituted phenyl is selected from one of the meanings given for R 4 in tables 3 or 4, in particular from 2- fluorophenyl, 3-fluorophenyl, 4-fluorophenyl, 2,4-difluorophenyl, 3,4-difluorophenyl, 3,5- difluorophenyl, 2,6-difluorophenyl, 2,4,6-trifluorophenyl, 2-chlorophenyl, 3-chlorophenyl, 3,5-dichlorophenyl, 2,6-dichlorophenyl, 4-chlorophenyl, 2-fluoro-4-chlorophenyl, 3- fluoro-4-trifluoromethylphenyl, 3,4,5-trifluorophenyl, 2-triflu
• the compounds of the formula I may be readily synthesized using techniques generally known by synthetic organic chemists. Exemplary synthesis methods are described for example in WO 87/06133.
• acyl hydrazides can be reacted with aldehydes or ketones to form acyl hydrazones:
• Cinnamic aldehydes and analogous ketones can be obtained according to a literature procedure (Organikum, Johann Ambrosius Barth Verlag, Heidelberg, 1996, pp. 493- 495) from benzaldehydes and aliphatic ketones or aldehydes.
• carboxylic acid esters Ar-(CH 2 ) n -COOR a
• Ar-(CH 2 ) n -COY halogen
• carboxylic acids Ar-(CH 2 ) n -COOH
• a coupling reagent such as DCC or DIC (according to Guan, Green, Bergstrom, J. Comb. Chem. 2000, 2, 297-300), and subsequent removal of the protecting group (Messina, Botta, Corelli, Paladino, Tetrahedron Asymm. 2000, 11 , 4895-4901 ; Greene, Wuts, Protective Groups in Organic Synthesis, 2nd edition, 1991 , pp. 309):
• R a C C 10 -alkyl
• the preparation of the compounds of formula I may lead to them being obtained as isomer mixtures (stereoisomers, enantiomers). If desired, these can be resolved by the methods customary for this purpose, such as crystallization or chromatography, also on optically active adsorbate, to give the pure isomers.
• the compounds of the general formula I are used for controlling harmful insects and arachnids.
• they are used for controlling the following animal pests:
• insects from the order of the lepidopterans for example Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, A ⁇ tographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheima- tobia brumata, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unip ⁇ ncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandi- osella, Earias insulana, Elasmopalpus lignosell ⁇ s, Eupoecilia ambig ⁇ ella, Evetria bo ⁇ - liana, Feltia subterranea, Galleria mellonella, Grapholitha funebrana, Grapholitha mo
• beetles Coldeoptera
• Agrilus sinuatus for example Agrilus sinuatus, Agriotes lineatus, Agriotes obscu- rus, Amphimallus solstitialis, Anisandrus dispar, Anthonomus grandis, Anthonomus pomorum, Atomaria linearis, Blastophagus piniperda, Blitophaga undata, Bruchus rufi- manus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cero- toma trifurcata, Ceuthorrhynchus assimilis, Ceuthorrhynchus napi, Chaetocnema tibi- alis, Conoderus vespertinus, Crioceris asparagi, Diabrotica longicornis, Diabrotica 12- punctata, Diabrotica virgifera, Epilachna varivestis, Epitrix hir
• dipterans dipterans
• Aedes aegypti Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Ceratitis capitata, Chrysomya bezziana, Chrysomya homi- nivorax, Chrysomya macellaria, Contarinia sorghicola, Cordylobia anthropophaga, Culex pipiens, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Fannia canicu- laris, Gasterophilus intestinalis, Glossina morsitans, Haematobia irritans, Haplodiplosis equestris, Hylemyia platura, Hypoderma lineata, Liriomyza sativae, Liriomyza trifolii, Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycor
• thrips (Thysanoptera), e.g. Dichromothrips corbetti, Frankliniella fusca, Frankliniella occidentalis, Frankliniella tritici, Scirtothrips citri, Thrips oryzae, Thrips palmi and Thrips tabaci,
• Hymenopterans e.g. Athalia rosae, Atta cephalotes, Atia sexdens, Atta texana, Hoplocampa minuta, Hoplocampa testudinea, Monomorium pharaonis, So- lenopsis geminata and Solenopsis invicta,
• Heteroptera e.g. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis and Thyanta perditor, homopterans (Homoptera), e.g.
• Heteroptera e.g. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris
• Acyrthosiphon onobrychis Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis forbesi, Aphis pomi, Aphis gossypii, Aphis grossulariae, Aphis schneideri, Aphis spiraecola, Aphis sambuci, Acyrthosiphon pisum, Aulacorthum solani, Bemisia argentifolii, Brachycaudus cardui, Brachycaudus helichrysi, Brachy- caudus persicae, Brachycaudus prunicola, Brevicoryne brassicae, Capitophorus horni, Cerosipha gossypii, Chaetosiphon fragaefolii, Cryptomyzus ribis, Dreyfusia nordman- nianae, Dreyfusia piceae, Dysa
• Isoptera e.g. Calotermes flavicollis, Leucotermes flavipes, Reticulitermes lucifugus und Termes natalensis,
• orthopterans e.g. Acheta domestica, Blatta orientalis, Blattella germanica, Forficula auricularia, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femur-rubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Periplaneta americana, Schistocerca ameri- cana, Schistocerca peregrina, Stauronotus maroccanus and Tachycines asynamorus,
• Orthoptera e.g. Acheta domestica, Blatta orientalis, Blattella germanica, Forficula auricularia, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femur-rubrum, Melan
• Arachnoidea such as arachnids (Acarina), e.g. of the families Argasidae, Ixodidae and Sarcoptidae, such as Amblyomma americanum, Amblyomma variegatum, Argas persi- cus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ornithodorus mou- bata, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus appendi- culatus, Rhipicephalus evertsi, Sarcoptes scabiei, and Eriophyidae spp.
• Arachnids Acarina
• Argasidae e.g. of the families Argas
• Tetranychidae spp. such as Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri, and oligonychus pratensis.
• the compounds of the formula I are preferably used for controlling pests of the orders Lepidoptera, Thysanoptera, Homoptera and Acarina and more preferably for controlling insects of the orders Lepidoptera and Homoptera.
• the compounds of formula (I) may be used to protect growing plants and crops from attack or infestation by insects or arachnids by contacting the plant/crop with a pesti- cidally effective amount of compounds of formula (I).
• crop refers both to growing and harvested crops.
• the insect, arachnid, plant and/or soil or water in which the plant is growing can be contacted with the present compound(s) I or composition(s) containing them by any application method known in the art.
• "contacting” includes both direct contact (applying the compounds/compositions directly on the insect, arachnid, and/or plant - typically to the foliage, stem or roots of the plant) and indirect contact (applying the compounds/compositions to the locus of the insect, arachnid, and/or plant).
• insects or arachnids may be controlled by contacting the target pest, its food supply or its locus with a pesticidally effective amount of compounds of formula (I).
• the application may be carried out before or after the infection of the locus, growing crops, or harvested crops by the pest.
• “Locus” means a habitat, breeding ground, plant, seed, soil, area, material or environment in which a pest or parasite is growing or may grow.
• the rate of application of the compounds and/or compositions of this invention may be in the range of about 0.1 g to about 4000 g per hectare, desirably from about 25 g to about 600 g per hectare, more desirably from about 50 g to about 500 g per hectare.
• the typical rate of application is of from about 1 g to about 500 g per kilogram of seeds, desirably from about 2 g to about 300 g per kilogram of seeds, more desirably from about 10 g to about 200 g per kilogram of seeds.
• Customary application rates in the protection of materials are, for example, from about 0.001 g to about 2000 g, desirably from about 0.005 g to about 1000 g, of active compound per cubic meter of treated material.
• the compounds I can be converted into the customary formulations, e.g. solutions, emulsions, microemulsions, suspensions, flowable concentrates, dusts, powders, pastes and granules.
• the use form depends on the particular purpose; in any case, it should guarantee a fine and uniform distribution of the compound according to the invention.
• the formulations are prepared in a known manner, e.g. by extending the active ingre-h with solvents and/or carriers, if desired using emulsifiers and dispersants, it also being possible to use other organic solvents as auxiliary solvents if water is used as the diluent.
• auxiliary solvents e.g. water is used as the diluent.
• Auxiliaries which are suitable are essentially: solvents such as aromatics (e.g. xylene), chlorinated aromatics (e.g. chlorobenzenes), paraffins (e.g. mineral oil fractions), alcohols (e.g. methanol, butanol), ketones (e.g. cyclohexanone), amines (e.g.
• ethanolamine, dimethylformamide and water
• carriers such as ground natural minerals (e.g. kaolins, clays, talc, chalk) and ground synthetic minerals (e.g. highly-disperse silica, silicates); emulsifiers such as non-ionic and anionic emulsifiers (e.g. polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignin-sulfite waste liquors and methylcellulose.
• ground natural minerals e.g. kaolins, clays, talc, chalk
• ground synthetic minerals e.g. highly-disperse silica, silicates
• emulsifiers such as non-ionic and anionic emulsifiers (e.g. polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignin-sulfite waste liquor
• Suitable surfactants are alkali metal, alkaline earth metal and ammonium salts of ligno- sulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates and fatty acids and their alkali metal and alkaline earth metal salts, salts of sulfated fatty alcohol glycol ether, condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of napthalenesulfonic acid with phenol or formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctylphenol, octyl- phenol, nonylphenol, alkyl
• Substances which are suitable for the preparation of directly sprayable solutions, emul- sions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g.
• benzene toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol, cyclohexa- none, chlorobenzene, isophorone, strongly polar solvents, e.g. dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone and water.
• strongly polar solvents e.g. dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone and water.
• Powders, materials for scattering and dusts can be prepared by mixing or concomi- tantly grinding the active substances with a solid carrier.
• Granules e.g. coated granules, compacted granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers.
• solid carriers are mineral earths, such as silicas, silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
• mineral earths such as silicas, silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk,
• compositions of the present invention include a formula I compound of this invention (or combinations thereof) admixed with one or more agronomi- cally acceptable inert, solid or liquid carriers.
• Those compositions contain a pesticidally effective amount of said compound or compounds, which amount may vary depending upon the particular compound, target pest, and method of use.
• the formulations comprise of from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active ingredient.
• the active ingredients are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
• V. 80 parts by weight of a compound of formula I are mixed thoroughly with 3 parts by weight of sodium diisobutylnaphthalene-alpha-sulfonate, 10 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 7 parts by weight of pulverulent silica gel, and the mixture is ground in a hammer mill (comprises 80% by weight of active ingredient).
• the active ingredients can be used as such, in the form of their formulations or the use forms prepared therefrom, e.g. in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, materials for spreading, or granules, by means of spraying, atomizing, dusting, scattering or pouring.
• the use forms depend entirely on the intended purposes; in any case, this is intended to guarantee the finest possible distribution of the active ingredients according to the invention.
• Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water.
• emulsions, pastes or oil dispersions the substances as such or dissolved in an oil or solvent, can be homogenized in water by means of wetter, tackifier, dispersant or emulsifier.
• concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil and such concentrates are suitable for dilution with water.
• the active ingredient concentrations in the ready-to-use products can be varied within substantial ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1%.
• the active ingredients may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active ingredient, or even the active ingredient without additives.
• UUV ultra-low-volume process
• compositions to be used according to this invention may also contain other active ingredients, for example other pesticides, insecticides, herbicides, fertilizers such as ammonium nitrate, urea, potash, and superphosphate, phytotoxicants and plant growth regulators, safeners and nematicides.
• additional ingredients may be used sequentially or in combination with the above-described compositions, if appropriate also added only immediately prior to use (tank mix).
• the plant(s) may be sprayed with a composition of this invention either before or after being treated with other active ingredients.
• agents can be admixed with the agents used according to the invention in a weight ratio of 1:10 to 10:1. Mixing the compounds I or the compositions comprising them in the use form as pesticides with other pesticides frequently results in a broader pesticidal spectrum of action.
• Organophosphates Acephate, Azinphos-methyl, Chlorpyrifos, Chlorfenvinphos, Diazi- non, Dichlorvos, Dicrotophos, Dimethoate, Disulfoton, Ethion, Fenitrothion, Fenthion, Isoxathion, Malathion, Methamidophos, Methidathion, Methyl-Parathion, Mevinphos, Monocrotophos, Oxydemeton-methyl, Paraoxon, Parathion, Phenthoate, Phosalone, Phosmet, Phosphamidon, Phorate, Phoxim, Pirimiphos-methyl, Profenofos, Prothiofos, Sulprophos, Triazophos, Trichlorfon;
• Pyrethroids Bifenthrin, Cyfluthrin, Cypermethrin, Deltamethrin, Esfenvalerate, Ethofen- prox, Fenpropathrin, Fenvalerate, Cyhalothrin, Lambda-Cyhalothrin, Permethrin, Si- lafluofen, Tau-Fluvalinate, Tefluthrin, Tralomethrin, Zeta-Cypermethrin;
• Arthropod growth regulators a) chitin synthesis inhibitors: benzoylureas: Chlorflua- zuron, Diflubenzuron, Flucycloxuron, Flufenoxuron, Hexaflumuron, Lufenuron, Novalu- ron, Teflubenzuron, Triflumuron; Buprofezin, Diofenolan, Hexythiazox, Etoxazole, Clofentazine; b) ecdysone antagonists: Halofenozide, Methoxyfenozide, Tebufenozide; c) juvenoids: Pyriproxyfen, Methoprene, Fenoxycarb; d) lipid biosynthesis inhibitors: Spirodiclofen;
• HPLC column RP-18 column(Chromolith Speed ROD from Merck KgaA, Germany).
• each of the compounds listed in table 4 show insecitcidal activity against at least one of the mentioned insect species or against an aphid species when applied in low application rates, e.g. at an application rate of 500 ppm or lower.
• the active compounds were formulated for testing the activity against insects and arachnids as a 10.000 ppm solution in a mixture of 35% acetone and water, which was diluted with water, if needed.
• a Sieva lima bean leaf expanded to 7-8 cm in length is dipped in the test solution with agitation for 3 seconds and allowed to dry in a hood.
• the leaf is then placed in a 100 x 10 mm petri dish containing a damp filter paper on the bottom and ten 2nd instar cater- pillars.
• 5 days observations are made of mortality, reduced feeding, or any interference with normal molting.
• the active compounds were formulated in 50:50 acetone:water and 100 ppm Kinetic ® surfactant.
• Cotton plants at the cotyledon stage were infested by placing a heavily infested leaf from the main colony on top of each cotyledon. The aphids were allowed to transfer to the host plant overnight, and the leaf used to transfer the aphids was removed. The cotyledons were dipped in the test solution and allowed to dry. After 5 days, mortality counts were made.
• the active compounds were formulated in 50:50 acetone:water and 100 ppm Kinetic ® surfactant.
• Pepper plants in the 2 nd leaf-pair stage (variety 'California Wonder') were infested with approximately 40 laboratory-reared aphids by placing infested leaf sections on top of the test plants. The leaf sections were removed after 24 hr. The leaves of the intact plants were dipped into gradient solutions of the test compound and allowed to dry. Test plants were maintained under fluorescent light (24 hour photoperiod) at about 25°C and 20-40% relative humidity. Aphid mortality on the treated plants, relative to mortality on check plants, was determined after 5 days.
• the active compounds were formulated in 50:50 acetone:water and 100 ppm Kinetic ® surfactant.
• Nasturtium plants grown in Metro mix in the 1 st leaf-pair stage were infested with approximately 2-30 laboratory-reared aphids by placing infested cut plants on top of the test plants. The cut plants were removed after 24 hr. Each plant was dipped into the test solution to provide complete coverage of the foliage, stem, protruding seed surface and surrounding cube surface and allowed to dry in the fume hood. The treated plants were kept at about 25°C with continuous fluorescent light. Aphid mortality was determined after 3 days.
• the active compounds were formulated in 50:50 acetone:water and 100 ppm Kinetic ® surfactant.
• Selected cotton plants were grown to the cotyledon state (one plant per pot).
• the cotyledons were dipped into the test solution to provide complete coverage of the foliage and placed in a well-vented area to dry.
• Each pot with treated seedling was placed in a plastic cup and 10 to 12 whitefly adults (approximately 3-5 day old) were introduced.
• the insects were colleted using an aspirator and an 0.6 cm, non-toxic Tygon ® tubing (R-3603) connected to a barrier pipette tip.
• the tip, containing the collected insects was then gently inserted into the soil containing the treated plant, allowing insects to crawl out of the tip to reach the foliage for feeding.
• the cups were covered with a reusable screened lid (150 micron mesh polyester screen PeCap from Tetko Inc). Test plants were maintained in the holding room at about
• the active compounds were formulated in 50:50 acetone:water and 100 ppm Kinetic ® surfactant.
• Sieva lima bean plants with primary leaves expanded to 7-12 cm were infested by plac- ing on each a small piece from an infested leaf (with about 100 mites) taken from the main colony. This was done at about 2 hours before treatment to allow the mites to move over to the test plant to lay eggs. The piece of leaf used to transfer the mites was removed. The newly-infested plants were dipped in the test solution and allowed to dry. The test plants were kept under fluorescent light (24 hour photoperiod) at about 25 °C and 20 - 40% relative humidity. After 5 days, one leaf was removed and mortality counts were made.
• Dichromothrips corbetti adults used for bioassay were obtained from a colony maintained continuously under laboratory conditions.
• the test com- pound was diluted to a concentration of 500 ppm (wt compound: vol diluent) in a 1 :1 mixture of acetone: water, plus 0.01% Kinetic ® surfactant.
• Thrips potency of each compound was evaluated by using a floral-immersion technique.
• Plastic petri dishes were used as test arenas. All petals of individual, intact or- chid flowers were dipped into treatment solution for approximately 3 seconds and allowed to dry for 2 hours. Treated flowers were placed into individual petri dishes along with 10 - 15 adult thrips. The petri dishes were then covered with lids. All test arenas were held under continuous light and a temperature of about 28°C for duration of the assay. After 4 days, the numbers of live thrips were counted on each flower, and along inner walls of each petri dish. The level of thrips mortality was extrapolated from pre- treatment thrips numbers.

Landscapes

• Life Sciences & Earth Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• Environmental Sciences (AREA)
• Agronomy & Crop Science (AREA)
• Engineering & Computer Science (AREA)
• Dentistry (AREA)
• General Health & Medical Sciences (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• Plant Pathology (AREA)
• Pest Control & Pesticides (AREA)
• Health & Medical Sciences (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Plural Heterocyclic Compounds (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
• Pretreatment Of Seeds And Plants (AREA)
• Heterocyclic Compounds Containing Sulfur Atoms (AREA)
• Furan Compounds (AREA)
• Pyridine Compounds (AREA)
• Indole Compounds (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=33490563

Family Applications (1)

Country Status (11)

Families Citing this family (10)

Family Cites Families (3)

• 2004
  • 2004-05-26 MX MXPA05012226A patent/MXPA05012226A/es not_active Application Discontinuation
  • 2004-05-26 BR BRPI0410626-1A patent/BRPI0410626A/pt not_active IP Right Cessation
  • 2004-05-26 AU AU2004243492A patent/AU2004243492A1/en not_active Abandoned
  • 2004-05-26 AR ARP040101810A patent/AR045688A1/es unknown
  • 2004-05-26 WO PCT/EP2004/005681 patent/WO2004105488A1/en active Search and Examination
  • 2004-05-26 EP EP04734834A patent/EP1631143A1/de not_active Withdrawn
  • 2004-05-26 JP JP2006529926A patent/JP2006528955A/ja not_active Withdrawn
  • 2004-05-26 CN CNA2004800146224A patent/CN1842272A/zh active Pending
  • 2004-05-26 KR KR1020057022609A patent/KR20060019558A/ko not_active Application Discontinuation
  • 2004-05-27 CL CL200401296A patent/CL2004001296A1/es unknown
• 2005
  • 2005-12-22 ZA ZA200510406A patent/ZA200510406B/xx unknown

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events