KR880006161A - 3위치에 포함된 할로겐화 사슬을 갖는 2,2-디메틸시클로프로판 카르복실산의 신규유도체, 이들을 제조하기 위한 방법 및 중간체, 살충제로서 이들의 용도 및 이들을 함유하는 조성물 - Google Patents
3위치에 포함된 할로겐화 사슬을 갖는 2,2-디메틸시클로프로판 카르복실산의 신규유도체, 이들을 제조하기 위한 방법 및 중간체, 살충제로서 이들의 용도 및 이들을 함유하는 조성물 Download PDFInfo
- Publication number
- KR880006161A KR880006161A KR870013093A KR870013093A KR880006161A KR 880006161 A KR880006161 A KR 880006161A KR 870013093 A KR870013093 A KR 870013093A KR 870013093 A KR870013093 A KR 870013093A KR 880006161 A KR880006161 A KR 880006161A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- formula
- atom
- compound
- alk
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 8
- 239000002917 insecticide Substances 0.000 title claims 2
- 238000000034 method Methods 0.000 title claims 2
- BFNMOMYTTGHNGJ-UHFFFAOYSA-N 2,2-dimethylcyclopropane-1-carboxylic acid Chemical class CC1(C)CC1C(O)=O BFNMOMYTTGHNGJ-UHFFFAOYSA-N 0.000 title 1
- 239000000543 intermediate Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 28
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 13
- 125000000217 alkyl group Chemical group 0.000 claims 11
- -1 methylenedioxy group Chemical group 0.000 claims 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 8
- 239000004480 active ingredient Substances 0.000 claims 7
- 125000005843 halogen group Chemical group 0.000 claims 7
- 150000002148 esters Chemical class 0.000 claims 6
- 239000000047 product Substances 0.000 claims 6
- 239000003795 chemical substances by application Substances 0.000 claims 5
- GXUQMKBQDGPMKZ-UHFFFAOYSA-N 2-hydroxy-2-(3-phenoxyphenyl)acetonitrile Chemical compound N#CC(O)C1=CC=CC(OC=2C=CC=CC=2)=C1 GXUQMKBQDGPMKZ-UHFFFAOYSA-N 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 125000000524 functional group Chemical group 0.000 claims 4
- 244000045947 parasite Species 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 229910052802 copper Inorganic materials 0.000 claims 3
- 239000010949 copper Substances 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- GPTFURBXHJWNHR-UHFFFAOYSA-N protopine Chemical compound C1=C2C(=O)CC3=CC=C4OCOC4=C3CN(C)CCC2=CC2=C1OCO2 GPTFURBXHJWNHR-UHFFFAOYSA-N 0.000 claims 3
- 229920006395 saturated elastomer Polymers 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 125000004434 sulfur atom Chemical group 0.000 claims 3
- KGANAERDZBAECK-UHFFFAOYSA-N (3-phenoxyphenyl)methanol Chemical compound OCC1=CC=CC(OC=2C=CC=CC=2)=C1 KGANAERDZBAECK-UHFFFAOYSA-N 0.000 claims 2
- AFEOKIGLYCQHAZ-UHFFFAOYSA-N (5-benzylfuran-3-yl)methanol Chemical compound OCC1=COC(CC=2C=CC=CC=2)=C1 AFEOKIGLYCQHAZ-UHFFFAOYSA-N 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- 241001465754 Metazoa Species 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 230000000855 fungicidal effect Effects 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- 241000238876 Acari Species 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- XLOPRKKSAJMMEW-SFYZADRCSA-N Chrysanthemic acid Natural products CC(C)=C[C@@H]1[C@@H](C(O)=O)C1(C)C XLOPRKKSAJMMEW-SFYZADRCSA-N 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- SYKNUAWMBRIEKB-UHFFFAOYSA-N [Cl].[Br] Chemical compound [Cl].[Br] SYKNUAWMBRIEKB-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000003302 alkenyloxy group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 1
- 244000000054 animal parasite Species 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 claims 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims 1
- 239000003638 chemical reducing agent Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- XLOPRKKSAJMMEW-UHFFFAOYSA-N chrysanthemic acid Chemical compound CC(C)=CC1C(C(O)=O)C1(C)C XLOPRKKSAJMMEW-UHFFFAOYSA-N 0.000 claims 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-M cyclopropanecarboxylate Chemical compound [O-]C(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-M 0.000 claims 1
- 230000008029 eradication Effects 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 230000000749 insecticidal effect Effects 0.000 claims 1
- 239000013067 intermediate product Substances 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 230000001069 nematicidal effect Effects 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 1
- CKFBFQHBUCDOHL-UHFFFAOYSA-N phenoxy(phenyl)methanol Chemical compound C=1C=CC=CC=1C(O)OC1=CC=CC=C1 CKFBFQHBUCDOHL-UHFFFAOYSA-N 0.000 claims 1
- 239000002689 soil Substances 0.000 claims 1
- 125000001174 sulfone group Chemical group 0.000 claims 1
- 150000003462 sulfoxides Chemical class 0.000 claims 1
- 230000002195 synergetic effect Effects 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
- C07D213/647—One oxygen atom attached in position 2 or 6 and having in the molecule an acyl radical containing a saturated three-membered ring, e.g. chrysanthemumic acid esters
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/14—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic radicals
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus as a ring member
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/41—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton
- C07C309/42—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton having the sulfo groups bound to carbon atoms of non-condensed six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
- C07C309/65—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
- C07C309/65—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
- C07C309/66—Methanesulfonates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C61/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C61/16—Unsaturated compounds
- C07C61/40—Unsaturated compounds containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C69/757—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
-
- 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/18—Radicals substituted by singly bound oxygen or sulfur atoms
- C07D317/24—Radicals substituted by singly bound oxygen or sulfur atoms esterified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/117—Esters of phosphoric acids with cycloaliphatic alcohols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/177—Esters of thiophosphoric acids with cycloaliphatic alcohols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/58—Pyridine rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/65502—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/6574—Esters of oxyacids of phosphorus
- C07F9/65742—Esters of oxyacids of phosphorus non-condensed with carbocyclic rings or heterocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Polymers & Plastics (AREA)
- Animal Husbandry (AREA)
- Food Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Pyrane Compounds (AREA)
- Furan Compounds (AREA)
- Indole Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (25)
- 다음식(I)을 갖는 화합물:상기식에서, X1및 X2는 서로 같거나 또는 다르고, 각각 할로겐원자를 나타내고, R1은 할로겐원자 C8이하를 함유하는 알킬기, 임의로 치환된C8이하를 함유하는 아릴기, C14이하를 함유하는 과플루오로 알킬기, 기기 R'이 C8이하를 함유하는 알킬기를 나타내는기이고.Y는 다음으로 구성되는 그룹으로 부터 선택된 기를 나타내고: -SO2alk1기(alk는 하나 또는 그 이상의 작용그룹에 의해 임의로 치환되고 포화되거나 또는 불포화된 선형 또는 측쇄알킬기를 나타냄): -SO2Ar기(Ar는 하나 또는 그 이상의 작용그룹에 의해 임의로 치환된 C14이하를 함유하는 알릴기를 나타냄):식중, alk2및 alk3는 서로 같거나 또는 다르고, 하나 또는 그 이상의 작용그룹에 의해 임의로 치환된 C8이하를 함유하는 포화되거나 또는 불포화된 직쇄 또는 측쇄 알킬기를 나타내거나 alk2및 alk3는기와 더불어 구리을 형성할 수 있고, A는 C6이하를 함유하고, 하나 또는 그 이상의 작용그룹에 의해 임의로 치환되고 포화되거나 또는 불포화된 직쇄 또는 측쇄탄화수소를 나타냄):-기(식중 alk'2및 alk'3는 alk2및 alk3와 같은 값을 나타냄) : -기(식중, R"은 하나 또는 그 이상의 작용그룹에 의해 임의로 치환된 알킬기 또는 알킬기를 나타냄) 그리고, R은 수소원자. C8이하를 함유하는 알킬기 또는 파레트리노이드 에스테르의 합성에 사용된 알코올의 잔기를 나타낸다.
- 제1항에 있어서, X1및 X2가 염소, 브롬, 또는 요오드원자를 나타내는 식(I)을 갖는 화합물.
- 제2항에 있어서, X1및 X2가 브롬원자 나타내는 식(I)을 갖는 화합물.
- 제1 내지 3항중 어느 한 항에 있어서, R1이 브롬 염소 또는 불소원자를 나타내는 식(I)을 갖는 화합물.
- 제1 내지 3항중 어느 한 항에 있어서, R1이 트리플루오로메틸기를 나타내는 식(I)을 갖는 화합물.
- 제1 내지 5항중 어느 한 항에 있어서, Y는 SO2alk1기(식중, alk1은 C8이하를 함유하는 알킬 또는 알케닐 기를 나타냄)를 나타내는 식(I)을 갖는 화합물.
- 제6항에 있어서, Y는 SO2CH3기를 나타내는 식(I)을 갖는 화합물.
- 제1 내지 5항중 어느 한 항에 있어서, Y는 SO2Ar기(식중, Ar은 상기에 정의한 바와 같음)를 나타내는 식(I)을 갖는 화합물.
- 제1 내지 8항중 어느 한 항에 있어서, R이 다음기를 나타내는 식(I)을 갖는 화합물. -수소원자,- 또는 C1내지 C8을 함유하는 임의로 치환된 직쇄 또는 측쇄알킬기, -또는 다음기로 구성되는 그룹으로 부터 선택된 하나 또는 그 이상의 기로 임의로 치환된 벤질기: C1내지 C4을 함유하는 알킬기, C2내지 C6을 함유하는 알케닐기, C2내지 C6을 함유하는 알케닐옥시기, C4내지 C8을 함유하는 알카디에닐기, 메틸렌디옥시기 및 할로겐원자, -또는 다음그룹:상기식에서, 치환체 R"은 수소원자 또는 메틸기를 나타내고, 치환체 R2는 모노시클릭아릴 또는 -C=CH 기 및 특히 5-벤질 3-푸릴메틸기를 나타낸다.-또는 다음 그룹:상기식에서, a는 수소원자 또는 메틸기를 나타내고, R3C2내지 C6을 함유하거나 또는 하나 또는 그 이상의 탄소-탄소불포화를 함유하는 지방족 유기기 및 특히 다음기중의 어느 하나를 나타낸다: -CH2-CH=CH2CH2-CH=CH3-CH2-CH-CH=CH2-CH2-CH-CH=CH2-CH2-C=CH, -또는 다음그룹:상기식에서, a는 수소원자 또는 메틸기를 나타내고, R3는 상기에 정의한바와 같고, R'1및 R'2은 같거나 또는 다르고, 수소원자, 할로겐원자, C1내지 C6을 함유하는 알킬기, C6내지 C1O을 함유하는 아릴기, C2내지 C5을 함유하는 알킬옥시카르보닐기 또는 시아노그룹을 나타낸다.-또는 다음그룹:상기식에서 B'는 산소 또는 황원자,또는 -CH2그룹 또는 술폭사이드 또는 술폰그룹을 나타내고, R4는 수소원자, -C=N 기, 메틸기, -CONH2기, -CSNH2기 또는 -C=CH 기를 나타내고, R5는 할로겐 원자 또는 메틸기를 나타내고 n은 0.1 또는 2의 정수이고, 특히 다음그룹중의 어느하나를 나타낸다: -3-페녹시벤질, 알파-시아노 3-페녹시 벤질, 알파-이티닐 3-페녹시벤질, 3-벤조일벤질, 1-3(3-페녹시페닐) 에틸 또는 알파-티오아미도 3-페녹시벤질.-또는 다음그룹:상기식에서, 치환체 R6, R7, R8및 R9는 수소원자, 염소원자 또는 메틸기를 나타내고, S/I는 방향족고리 또는 유사한 디히드로 또는 테트라히드로고리를 의미한다.-또는 다음그룹:-또는 다음그룹:상기식에서, R10은 수소원자 또는 CN 라티칼을 나타내고, R12는 -CH2-기 또는 산소원자를 나타내고, R11은과의 결합이 이용할 수 있는 위치중의 어느하나에서 발견될 수 있는 티아졸릴 또는 티아디아졸릴기를 나타내고, R12는 황원자와 질소원자사이에 포함된 탄소원자에 위해 R11과 결합된다.-또는 다음그룹:-또는 다음그룹:상기식에서, R13은 수소원자 또는 CN기를 나타낸다.-또는 다음그룹:상기식에서, R13은 상기에 정의한바와같고, 벤조일기는 위치 3 또는 4에 있다.-또는 다음그룹:상기식에서 R14는 수소원자, 메틸, 에틸, 또는 시아노기를 나타내고, R15및 R16은 다르고, 수소, 불소 또는 브롬원자를 나타낸다.-또는 다음그룹 :상기식에서, R14는 상기에 정의하였고, 각가의 R17은 독립적으로 C1내지 C4를 함유하는 알킬기, C1내지 C4를 함유하는 알콕시기, C1내지 C4를 함유하는 알킬티오가, C1내지 C4를 함유하는 알킬술포닐기, 트리플루오로메틸, 3,4-메틸렌디옥시, 클로로플루오로 또는 브로모그룹을 나타내고, P는 0.1 또는 2의 정수를 나타내고, B"은 산소원자 또는 황원자를 나타낸다.-또는 다음그룹:상기식에서, R18은 수소원자, 메틸, 에티닐 또는 시아노가를 나타내고, R19는 다르고, 수소, 불소 또는 브롬원자를 나타내고, Ar은 C14이하를 함유하는 알릴기를 나타낸다.-또는 다음그룹:
- 제9항에 있어서, R이 다음기를 나타내는 식(I)을 갖는 화합물:
- 제10항에 있어서, 다음 화합물명을 갖는 식(I)의 화합물:-시아노-(3-페녹시-페닐) 메틸 1R-[1-알파(S)3-알파-(R)] 2,2-디메틸-3-[1(메틸술포닉옥시)-2,2,2-트리브로모에틸] 시클로프로판 카르복실레이트.-시아노-(3-페녹시페닐) 메틸 1R-[1-알파(S)3-알파-(R)] 2,2-디메틸3-[3-[2,2,2-트리브로모-1-(메틸술포닉옥시에틸] 시클로프로판 카르복실레이트.-시아노-[(3-페녹시-4-플루오로) 페닐] 에틸 1R-[1-알파(S)3-알파-(R)] 2,2-디메틸-3-[2,2,2-트리브로모-1-(메틸술포닉옥시에틸) 시클로프로판 카르복실레이트.-[(2-메틸-3-페닐)페닐] 메틸1 R-[1-알파,3-알파-(RS,RS)]2,2-디메틸-3-[2트리플루오로메틸-2-브로모-2-클로로-1-메틸술포닉옥시에틸] 시클로프로판 카르복실레이트.-시아노-[(3-페녹시페닐)] 메틸-1R-[1-알파, 3-알파-(RS*,RS*)] 2,2-디메틸-3-[2-트리플루르메틸-2-브로모-2-클로로-1-메틸술포닐옥시에틸] 시클로프로판 카르복실레이트.
- 염기의 존재하에 다음식(Ⅱ)을 갖는 화합물을 다음식(Ⅳ)을 갖는 화합물 반응시켜 다음식(Ⅳ)의 화합물을 얻고, 이를 술포닐화제, 포스포닐화제, 티포스릴화제 또는 아실화제와 반응시켜 다음식(I)을 갖는 해당하는 화합물을 얻고, 해당 하는 산으로 임의로 변화시키고, 임의로 에스테르화제와 반응 시킴을 특징으로 하는 제11항에 정의한 바와같은 식(I)을 갖는 화합물의 제조방법:상기식에서 R은 상기에 정의한 바와 같다.상기식에서, X1,X2, 및 R1은 상기에 정의한 바와 같다.
- 중간체 생성물로서, X1,X2, 및 R1이 각각 할로겐원자를 나타내는 화합물을 제외하고 제12항에 정의한식(Ⅳ)을 갖는 화합물.
- 동, 식물의 기생충 및 토양의 기생충을 박멸하기 위한 제1 내지 11항중의 어느 한항에 정의한 식(I)을 갖는 화합물의 용도
- 활성성분으로서 제1 내지 11항중의 어느 한항에 정의한 생성물중의 적어도 어느 하나를 함유함을 특징으로 하는 식물의 기생충 및 온혈동물의 기생충을 박멸하기 위한 조성물.
- 활성성분으로서 제1 내지 11항중의 어느 한항에 정의한 생성물중의 적어도 어느 하나를 함유하는 살충제 조성물.
- 활성성분으로서 제1 내지 11항중의 어느 한항에 정의한 생성물중의 적어도 어느 하나를 함유하는 살진드기 조성물.
- 활성성분으로서 제1 내지 11항중의 어느 한항에 정의한 생성물중의 적어도 어느 하나를 함유하는 살선충 조성물.
- 활성성분으로서 제1 내지 11항중의 어느 한항에 정의한 생성물중의 적어도 어느 하나를 함유하는 온형동물의 기생충, 특히 진드기를 박멸하기위한 살진드기 조성물.
- 활성성분으로서 제1 내지 11항중의 어느 한항에 정의한 생성물중의 적어도 어느 하나를 함유하는 동물사료용 조성물.
- 활성성분으로서 한편으로 일반식(I)을 갖는 화합물들 중의 적어도 어느 하나 및 다른 한편으로, 크리스안템산과 더불어 알테트롤론, 2,4,5,6-테트라히드로프탈이미도 메틸알코올. 5-벤질 3-푸릴메틸알코올, 3-페녹시벤질알코올 및 알파-시아노 3-페녹시벤질 알코올의 에스테르:2,2-디메틸 3-(2-옥소 3,4,5,6,-테트라히드로티페닐리덴 메틸)시클로프로판-1-카르복실산과 더불어 5-벤질 3-푸릴메틸알코올의 에스테르:2,2-디메틸 3-2,2-디클로로비닐)시클로프로판-1-카르복실과 더불어 알파-시아노 3-페녹시 벤질알코올; 2,2-디메틸3-(2,2-디브로오비닐)시클로 프로판-1-카르복신산과 더불어 알파 시아노 3-페녹시 벤질 알코올의 에스테르:파라클로로페닐-2이 소프로필 아세트산과 더불어 3-페녹시 벤질알코올의 에스테르:2,2-디메틸 3-(1,2,2,2,-테트라할로에틸시클로프로판-1-카르복실산과 더불어 알레트롤론,3,4,5,6-테트라히드로프툿이미도 메틸알코올, 5-벤질 3-푸릴메틸 알코올 3-페녹시벤질 알코올 및 알파-시아노 3-페녹시벤질알코올의 에스 테르 ["할로" 는 불소, 염소 또는 브롬원자를 나타내고, 화합물(I)은 이들의 모든 가능한 입체이성체형태로 존재할 수 있고, 또한 상기에 제시한것처럼 피레트리노이드 에스테르의 산 및 알코올 결합일 수 있음]로 구성되는 그룹으로부터 선택된 피레트리노이드 에스테르중의 적어도 어느 하나를 함유함을 특징으로 하는 살충제, 살진드기제 또는 살선충제 활성이 부여된 결합.
- 제15 내지 21항중의 어느 한항에 파레트리노이드 상승효과를 추가로 함유함을 특징으로하는 조성물 및 결합.
- 식(I)을 갖는 화합물을 환원제와 반응시켜 다음식(Ⅲ)을 갖는 해당하는 화합물을 얻음을 특징으로 하는 제1내지 11항중의 어느 한항에 정의한 식(I)을 갖는 화합물의 용도:상기식에서 X1,R2, 및 R은 상기에 정의한 바와 같다.
- 식(I)을 갖는 화합물은 다음 식(I')에 해당하고 식(Ⅲ)을 갖는 화합물은 다음식(Ⅲ')에 해당함적 특징으로 하는 제23항의 용도:상기식에서, Y 및 R은 상기에 정의한 바와 같다.
- 식(I)을 갖는 화합물은 다음 식(I")을 갖는 화합물에 해당하고 식(Ⅲ)을 갖는 화합물은 다음식(Ⅲ")을 갖는 화합물에 해당함을 특징으로 하는 제23항의 용도:상기식에서, Y 및 R은 상기에 정의한 바와 같다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8616155A FR2607133B1 (fr) | 1986-11-20 | 1986-11-20 | Nouveaux derives de l'acide 2,2-dimethyl cyclopropane carboxylique portant en 3 une chaine halogenee saturee, leur procede de preparation et leur application comme pesticides |
FR86-16155 | 1986-11-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR880006161A true KR880006161A (ko) | 1988-07-21 |
KR960010787B1 KR960010787B1 (ko) | 1996-08-08 |
Family
ID=9341015
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019870013093A KR960010787B1 (ko) | 1986-11-20 | 1987-11-20 | 3위치에 포화된 할로겐화사슬을 갖는 2,2-디메틸 시클로프로판 카르복실산의 신규유도체, 이들을 제조하기 위한 방법 및 중간체, 살충제로서 이들의 용도 및 이들을 함유하는 조성물 |
Country Status (18)
Country | Link |
---|---|
US (2) | US4925874A (ko) |
EP (3) | EP0269514B1 (ko) |
JP (2) | JP2717787B2 (ko) |
KR (1) | KR960010787B1 (ko) |
CN (2) | CN1033028C (ko) |
AT (2) | ATE119516T1 (ko) |
AU (1) | AU593955B2 (ko) |
BR (1) | BR8706250A (ko) |
DE (3) | DE3781383T2 (ko) |
ES (3) | ES2062598T3 (ko) |
FR (1) | FR2607133B1 (ko) |
GR (1) | GR3005520T3 (ko) |
HU (1) | HU206075B (ko) |
MX (1) | MX9412A (ko) |
OA (1) | OA08693A (ko) |
PT (1) | PT86171B (ko) |
RU (1) | RU1779242C (ko) |
ZA (1) | ZA878666B (ko) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2607133B1 (fr) * | 1986-11-20 | 1989-05-05 | Roussel Uclaf | Nouveaux derives de l'acide 2,2-dimethyl cyclopropane carboxylique portant en 3 une chaine halogenee saturee, leur procede de preparation et leur application comme pesticides |
FR2608152B1 (fr) * | 1986-12-11 | 1989-03-31 | Roussel Uclaf | Le 2,2-dimethyl 3-formyl cyclopropane carboxylate de pentafluorophenylmethyle, son procede de preparation et son application a la synthese de produits pesticides |
AU610856B2 (en) * | 1987-02-24 | 1991-05-30 | Sandoz Ltd. | Alpha cyanobenzyl esters of cyclopropane carboxylic acids |
FR2636945B1 (fr) * | 1988-09-29 | 1991-04-19 | Roussel Uclaf | Nouveaux derives de l'acide 2,2-dimethyl 3-(1-hydroxy-2-sulfino-ethyl) cyclopropane carboxylique, leur procede de preparation et leur application comme pesticides |
DK171797B1 (da) * | 1995-07-21 | 1997-06-02 | Cheminova Agro As | Cyclopropanderivater og fremgangsmåde til fremstilling af cyclopropancarboxylsyrer, ved hvilken disse cyclopropanderivater indgår som mellemprodukter. |
US8466096B2 (en) * | 2007-04-26 | 2013-06-18 | Afton Chemical Corporation | 1,3,2-dioxaphosphorinane, 2-sulfide derivatives for use as anti-wear additives in lubricant compositions |
JP2022511964A (ja) * | 2018-12-11 | 2022-02-01 | セーセーエス 12 | 銀行支払いカードのセキュリティデータをセキュア化するためのデバイスおよび方法 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5850209B2 (ja) * | 1975-04-15 | 1983-11-09 | 住友化学工業株式会社 | 2 2− ジメチル−3−(2 2−ジハロビニル)−シクロプロパンカルボンサンユウドウタイノ セイゾウホウ |
GB1572183A (en) * | 1975-09-05 | 1980-07-23 | Wellcome Found | Cyclopropane carboxylic acid ester synthesis and intermediates therefor |
FR2396006A1 (fr) * | 1977-06-27 | 1979-01-26 | Roussel Uclaf | Nouveaux composes a noyau cyclopropanique, procede de preparation et application a la preparation de derives cyclopropaniques a chaine dihalovinyliques |
EP0021521B1 (en) * | 1979-07-03 | 1982-12-15 | Shell Internationale Researchmaatschappij B.V. | Process for the preparation of dihalovinyl compounds |
US4376785A (en) * | 1980-06-19 | 1983-03-15 | Sumitomo Chemical Company, Limited | Cyclopropanecarboxylates and a low fish toxic insecticide and/or acaricide containing them |
DE3037302A1 (de) * | 1980-10-02 | 1982-05-27 | Bayer Ag, 5090 Leverkusen | Bissilylierte l-hydroxycyclopropancarbonsaeuren, verfahren zu ihrer herstellung sowie ihre verwendung als zwischenprodukte |
GB2099810A (en) * | 1981-06-09 | 1982-12-15 | Shell Int Research | Cyclopropanecarboxylate esters and their use as pesticides |
FR2534252A1 (fr) * | 1982-10-12 | 1984-04-13 | Roussel Uclaf | Nouveaux derives de l'acide cyclopropane carboxylique substitues en 3 par une chaine vinylique elle-meme substituee, leur procede de preparation et leur application comme pesticides |
IT1206727B (it) * | 1985-01-11 | 1989-05-03 | Donegani Guido Ist | Processo per la preparazione di carbinoli polialogenati. |
JPH0674238B2 (ja) * | 1985-09-30 | 1994-09-21 | 財団法人相模中央化学研究所 | 2,2−ジメチルシクロプロパンカルボン酸誘導体 |
FR2607133B1 (fr) * | 1986-11-20 | 1989-05-05 | Roussel Uclaf | Nouveaux derives de l'acide 2,2-dimethyl cyclopropane carboxylique portant en 3 une chaine halogenee saturee, leur procede de preparation et leur application comme pesticides |
-
1986
- 1986-11-20 FR FR8616155A patent/FR2607133B1/fr not_active Expired
-
1987
- 1987-11-18 HU HU875123A patent/HU206075B/hu not_active IP Right Cessation
- 1987-11-18 MX MX941287A patent/MX9412A/es unknown
- 1987-11-19 AT AT91105958T patent/ATE119516T1/de not_active IP Right Cessation
- 1987-11-19 DE DE8787402605T patent/DE3781383T2/de not_active Expired - Fee Related
- 1987-11-19 EP EP87402605A patent/EP0269514B1/fr not_active Expired - Lifetime
- 1987-11-19 DE DE3751149T patent/DE3751149T2/de not_active Expired - Fee Related
- 1987-11-19 ZA ZA878666A patent/ZA878666B/xx unknown
- 1987-11-19 RU SU874203815A patent/RU1779242C/ru active
- 1987-11-19 EP EP91105956A patent/EP0445843B1/fr not_active Expired - Lifetime
- 1987-11-19 ES ES91105956T patent/ES2062598T3/es not_active Expired - Lifetime
- 1987-11-19 BR BR8706250A patent/BR8706250A/pt unknown
- 1987-11-19 EP EP91105958A patent/EP0451873B1/fr not_active Expired - Lifetime
- 1987-11-19 PT PT86171A patent/PT86171B/pt not_active IP Right Cessation
- 1987-11-19 ES ES87402605T patent/ES2051762T3/es not_active Expired - Lifetime
- 1987-11-19 ES ES91105958T patent/ES2069765T3/es not_active Expired - Lifetime
- 1987-11-19 DE DE3789064T patent/DE3789064T2/de not_active Expired - Fee Related
- 1987-11-20 US US07/123,374 patent/US4925874A/en not_active Expired - Lifetime
- 1987-11-20 AU AU81434/87A patent/AU593955B2/en not_active Ceased
- 1987-11-20 JP JP29224687A patent/JP2717787B2/ja not_active Expired - Fee Related
- 1987-11-20 OA OA59226A patent/OA08693A/xx unknown
- 1987-11-20 KR KR1019870013093A patent/KR960010787B1/ko active IP Right Grant
- 1987-11-20 CN CN87101182A patent/CN1033028C/zh not_active Expired - Fee Related
-
1989
- 1989-10-18 US US07/423,803 patent/US5082832A/en not_active Expired - Fee Related
-
1991
- 1991-04-15 AT AT91105956T patent/ATE101391T1/de active
-
1992
- 1992-08-27 GR GR920400799T patent/GR3005520T3/el unknown
-
1994
- 1994-11-18 JP JP30834994A patent/JP2710097B2/ja not_active Expired - Fee Related
-
1995
- 1995-10-07 CN CN95115659A patent/CN1125714A/zh active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1237135A (fr) | Esters d'acides cyclopropane carboxyliques apparentes a l'acide pyrethrique, leur procede de preparation, leur application a la lutte des parasites des vegetaux et des locaux,les compositions les renfermant et les nouveaux intermediaires obtenus | |
CA1084943A (en) | Pesticidal m-phenoxybenzyl esters of 2,2- dimethylspiro 2,4 heptane-1-carboxylic acid derivatives | |
KR880006161A (ko) | 3위치에 포함된 할로겐화 사슬을 갖는 2,2-디메틸시클로프로판 카르복실산의 신규유도체, 이들을 제조하기 위한 방법 및 중간체, 살충제로서 이들의 용도 및 이들을 함유하는 조성물 | |
DE2327660B2 (de) | Cyclopropancarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide | |
KR900011704A (ko) | 신규한 2,2-디메틸-3-(2-모노할로에테닐)시클로프로판 카르복실산 유도체, 그의 제조방법 및 그의 살충제로서의 용도 | |
FR2687149A1 (fr) | Nouveaux esters pyrethrinouides derives d'alcools thiazoliques, leur procede de preparation et leur application comme pesticides. | |
FR2687152A1 (fr) | Nouveaux esters pyrethrinouides derives d'alcool furanique ou thiophenique, leur procede de preparation et leur application comme pesticides. | |
FR2547580A1 (fr) | Cyclopropane carboxylates comportant un groupement cyane sur la chaine laterale du cyclopropane, leurs procedes de preparation, les intermediaires necessaires a la mise en oeuvre de ces procedes et les compositions les renfermant | |
US4537897A (en) | 3-(1,2-Propadienyl)-cyclopropane-carboxylates | |
US4356187A (en) | Novel esters of 2-methyl-3-allyl-4-substituted-cyclopent-2-ene-1-yl | |
ES2061516T3 (es) | Esteres fluorobencilicos. | |
FR2534252A1 (fr) | Nouveaux derives de l'acide cyclopropane carboxylique substitues en 3 par une chaine vinylique elle-meme substituee, leur procede de preparation et leur application comme pesticides | |
EP0133406A1 (fr) | Nouveaux dérivés de l'acide cyclopropane carboxylique, leur préparation, leur application à la lutte contre les parasites et les compositions les renfermant | |
EP0521780B1 (fr) | Nouveaux esters pyréthrinoides de l'alcool 1,3,4,5,6,7-hexahydro 1,3-dioxo 2H-isoindol-2-yl méthylique, leur procédé de préparation et leur application comme pesticides | |
JP3892009B2 (ja) | 2,2−ジメチル−3−(3,3,3−トリフルオル−1−プロペニル)シクロプロパンカルボン酸から誘導される新規のエステル、その製造方法及び害虫駆除剤としてのその使用 | |
CA1265808A (fr) | Derives de l'acide cyclopropane carboxylique a substituant iode, leur preparation, leur application a la lutte contre les parasites des vegetaux et des animaux et les compositions les renfermant | |
JPH026436A (ja) | 適宜なハロゲノビニル誘導体から出発するトリフルオルメチルビニル誘導体の新規の製造方法 | |
CA1239935A (fr) | Esters d'acides cyclopropane carboxyliques et d'alcools aliphatiques insatures, procede de preparation, leurs utilisations comme pesticides et pesticides les renfermant les compositions les contenant | |
CA1203538A (fr) | Derives de l'acide cyclopropane carboxylique comportant un groupement alcoylthiocarbonyle et un atome d'halogene, et leur procede de preparation | |
BE1002794A4 (fr) | Nouvelle composition herbicide. | |
FR2687666A1 (fr) | Nouveaux esters pyrethrinouiques, derives de l'alcool 6-(trifluoromethyl) benzylique, leur procede de preparation et leur application comme pesticides. | |
JP3320453B2 (ja) | 4−アミノ−2,3,5,6−テトラフルオルフェニルメチルアルコールの新規なピレスリノイドエステル、それらの製造法及びそれらのペスチサイドとしての用途 | |
EP0253536A3 (en) | Fluorobenzyl esters | |
FR2537973A1 (fr) | Esters d'acides cyclopropane carboxyliques et d'alcools aliphatiques insatures, leur procede de preparation et les compositions pesticides les renfermant | |
SU622387A3 (ru) | Инсектицидное средство |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
G160 | Decision to publish patent application | ||
E701 | Decision to grant or registration of patent right | ||
NORF | Unpaid initial registration fee |