KR910000649A - 살충제 - Google Patents
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- KR910000649A KR910000649A KR1019890007968A KR890007968A KR910000649A KR 910000649 A KR910000649 A KR 910000649A KR 1019890007968 A KR1019890007968 A KR 1019890007968A KR 890007968 A KR890007968 A KR 890007968A KR 910000649 A KR910000649 A KR 910000649A
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- 239000000575 pesticide Substances 0.000 title claims 3
- 150000001875 compounds Chemical class 0.000 claims abstract 20
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 11
- 239000001257 hydrogen Substances 0.000 claims abstract 11
- 125000005843 halogen group Chemical group 0.000 claims abstract 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 8
- 241000607479 Yersinia pestis Species 0.000 claims abstract 8
- 238000000034 method Methods 0.000 claims abstract 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract 6
- 125000003118 aryl group Chemical group 0.000 claims abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 3
- 125000005842 heteroatom Chemical group 0.000 claims abstract 3
- 150000002431 hydrogen Chemical class 0.000 claims abstract 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052799 carbon Inorganic materials 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 2
- 125000002950 monocyclic group Chemical group 0.000 claims abstract 2
- 125000006413 ring segment Chemical group 0.000 claims abstract 2
- 150000003839 salts Chemical class 0.000 claims abstract 2
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 claims abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract 2
- 208000015181 infectious disease Diseases 0.000 claims 7
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 239000002253 acid Substances 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 241000238421 Arthropoda Species 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
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 230000000855 fungicidal effect Effects 0.000 claims 2
- 239000000417 fungicide Substances 0.000 claims 2
- 239000002917 insecticide Substances 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Chemical group 0.000 claims 2
- 244000045947 parasite Species 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 1
- 239000000443 aerosol Substances 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 230000000749 insecticidal effect Effects 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims 1
- -1 phosphoro imidate ester Chemical class 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Chemical group 0.000 claims 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004276 dioxalanyl group Chemical group 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
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- 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
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
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- 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
- A01N37/36—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
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- 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
- A01N43/42—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 condensed with carbocyclic rings
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- 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
- A01N49/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds containing the group, wherein m+n>=1, both X together may also mean —Y— or a direct carbon-to-carbon bond, and the carbon atoms marked with an asterisk are not part of any ring system other than that which may be formed by the atoms X, the carbon atoms in square brackets being part of any acyclic or cyclic structure, or the group, wherein A means a carbon atom or Y, n>=0, and not more than one of these carbon atoms being a member of the same ring system, e.g. juvenile insect hormones or mimics thereof
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- C07C233/00—Carboxylic acid amides
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- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C233/11—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
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- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and unsaturated
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- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
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- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/70—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
- C07C45/71—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
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- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/687—Unsaturated compounds containing a keto groups being part of a ring containing halogen
- C07C49/697—Unsaturated compounds containing a keto groups being part of a ring containing halogen containing six-membered aromatic rings
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
- C07D215/227—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
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- C07D277/62—Benzothiazoles
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Quinoline Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (21)
- 하기 일반식(Ⅰ)의 화합물 또는 그것의 염; Q1Q(CR2=CR3)a(CR4=CF)(CR5=CR6)b(C=O)NHR1(I)상기식에서, Q1은 탄소, 및 선택적으로 적어도 하나의 고리가 방향족인 1이상의 헤테로원자로부터 선택되는 5또는 6개의 고리원자를 각각 함유한 모노사이클 또는 용융 비사이클 고리계이거나, 또는 Q1은 디할로비닐기이며: Q는 1-12개의 탄소원자 및 선택적으로 한 개 또는 2개의 산소원자 및/또는 불포화기 -CR7=CR8-또는 -C=C-(여기서, R7및 R8은 수소 또는 할로로부터 선택함)를 함유하는 알킬쇄이고: a는 0또는 1이며; b는 0또는 1이고, a와 b의 총합은 0또는 1이며: R2, R3, R4, R및5R6는 동일하거나 다른 수소, 할로 및 C1-4알킬로부터 독립적으로 선택되고: R1은 수소, 그리고, 디옥살알라닐, 할로, 시아노, 트리플루오로 메틸, 트리플루오로메틸티오 또는 C1-6알콕시에 의해 선택적으로 치환되는 C1-6하이드로카르빌이다.
- 제1항에 있어서, Q1이 질소, 산소, 황으로부터 선택되는 1이상의 헤테로원자를 함유하는 화합물.
- 제1항에 있어서, 헤테로사이클 Q1이 질소헤테로원자 및 선택적으로 부가적인 질소, 산소 또는 황헤테로원자를 함유하는 화합물.
- 제1항에 있어서, 고리계 Q1의 치환체가 할로, 시아노, C1-6알킬 및 C1-6알콕시로부터 선택되며 이들 각각은 선택적으로 1이상의 할로겐원자로 치환되거나, 또는 치환체는 m이 0,1또는 2, R9가 할로에 의해 선택적으로 치환되는 C1-6알킬인 기 S(O)mR9인 화합물.
- 제1항에 있어서, 고리계 Q1의 퀴놀린, 피리딘, 티아졸, 옥사졸, 벤조티아졸, 벤조옥사졸, 티아디아졸, 옥사디아졸, 페닐, 인다닐, 나프틸 및 테트라히드로나프틸인 화합물.
- 제1항에 있어서, Q는 산소원자가 Q1에 인접해 있는 CH2O(CH2)6, CH2, O(CH2)7또는 O(CH2)9기인 화합물.
- 제1항에 있어서, R2,R3가 수소이고, R4및 R5가 수소 및 메틸로부터 선택되며, R6가 수소 및 불소로부터 선택되는 화합물.
- 하기 일반식(IA)의 화합물:Q1QCH=CH,CCH3=CF.C(=O) NHR1상기식에서, Q1,Q 및 R1은 상기 정의한 바와 같다.
- 하기 일반식(IB)의 화합물:Q1QCH=CF,CR5=CR6.C(=O) NHR1상기식에서, R5는 수소 또는 메틸, R6는 수소 또는 불소, Q1,Q 및 R1은 상기 정의한 바와 같다.
- (2Z,4E)N-이소부틸-2-플루오로-3-메틸-12-(2-퀴놀리닐옥시)도데카-2,4-디엔아미드, (2Z,4E)N-이소부틸-2-플룽로-3-메틸-11-(3,5-비스트리플루오로메틸벤질옥시)운데카-2,4-디엔아미드, (2Z,4E)N-이소부틸-2-플루오로-3-메틸-6-(4-클로로-2-인다닐)헥사-2,4-디엔아미드, (2E,4Z)N-이소부틸-4-플루오로-12-(2-퀴놀리닐옥시)도데카-2,4디엔아미드, (2E,4Z)N-이소부틸-4-플루오로-3-메틸-12-(2-퀴놀리닐옥시)도데카-2,4-디엔아미드로부터 선택되는 화합물.
- a)아민 H2NR1과 상응하는 산 또는 산유도체Q1Q(CR2=CR3)a(CR4=CF)(CR5=CR6)bCOZ을 반응시키고, b)화합물 R6CHR10CONHR1과 알데히드 또는 케톤 Q1QCR4=CF·CR5(=O)를 반응시키는 것으로 구성되는 상기 일반식(Ⅰ)의 화합물의 제조방법: 상기식에서, Q,Q1,R2,R3,R4,R5,R6,a,b 및 R1은 상기한 바와 같으며, Z는 히드록시, C1-6알콕시, 할로 또는 포스포로 이미데이트 에스테르 -P(=O)(O-아릴) NH-아릴(여기서, 아릴은 C1-6아릴임)이고, R10은 Z2가 알킬, 알콕시(양호하게는 에톡시)또는 아릴(양호하게는 페닐)인 기(Z2)3P또는 (Z2)2P(->0)이다.
- 1이상의 담체 또는 희석제와 혼합하여 제1항 내지 제10항중의 한 항으로 정의된 일반식(Ⅰ)의 화합물로 구성되는 살충제제.
- 제12항에 있어서, 부가적으로 공력근 또는 상승작용제를 함유하는 살충제제.
- 제12항 또는 제13항에 있어서, 부가적으로 1이상의 살충작용성분, 친화제, 구산제, 살균제, 살진규제 및/또는 구충제를 함유하는 살충제제.
- 인간 또는 수의학에 사용하는 일반식(Ⅰ)의 화합물.
- 제1항 내지 제10항중의 어느 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)의 화합물을 절지동물 또는 기생충 또는 이들의 주위에 투여하는 것으로 구성되는 절지동물 또는 기생충의 구제 방법.
- 제1항 내지 제10항중의 어느 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)화합물을 해충감염에 민감한 식물에 투여하는 것으로 구성되는 식물에 대한 해충감염의 구제방법.
- 제1항 내지 제10항중의 어는 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)화합물을 해충감염에 민감한 저장 제품에 투여하는 것으로 구성되는 저장제품에 대한 해충감염의 구제방법.
- 제1항 내지 제10항중의 어느 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)화합물을 해충감염에 민감한 환경에 투여하는 것으로 구성되는 환경에 대한 해충감염의 구제방법.
- 제1항 내지 제10항중의 어느 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)화합물을 동물에 투여하는 것으로 구성되는 동물에 대한 해충감염의 구제방법.
- 제11항의 방법을 수반하는 신규하는 화학적 중간체.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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GB888813678A GB8813678D0 (en) | 1988-06-09 | 1988-06-09 | Pesticides |
GB8813678.3 | 1988-06-09 | ||
GB8823437.2 | 1988-10-06 | ||
GB888823437A GB8823437D0 (en) | 1988-10-06 | 1988-10-06 | Pesticides |
Publications (1)
Publication Number | Publication Date |
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KR910000649A true KR910000649A (ko) | 1991-01-29 |
Family
ID=26293990
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019890007968A KR910000649A (ko) | 1988-06-09 | 1989-06-08 | 살충제 |
Country Status (14)
Country | Link |
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US (1) | US5180737A (ko) |
EP (1) | EP0346107B1 (ko) |
JP (1) | JP2667908B2 (ko) |
KR (1) | KR910000649A (ko) |
AT (1) | ATE127790T1 (ko) |
AU (1) | AU619853B2 (ko) |
DE (1) | DE68924199T2 (ko) |
DK (1) | DK280189A (ko) |
EG (1) | EG19009A (ko) |
FI (1) | FI892819A (ko) |
HU (1) | HU207036B (ko) |
IL (1) | IL90568A0 (ko) |
NZ (1) | NZ229459A (ko) |
PT (1) | PT90790B (ko) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
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GB9113624D0 (en) * | 1991-06-25 | 1991-08-14 | Wellcome Found | Pesticides |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US4855086A (en) * | 1982-10-15 | 1989-08-08 | Burroughs Wellcome Co. | Novel pesticides, preparation and use |
US4713200A (en) * | 1984-04-03 | 1987-12-15 | Burroughs Wellcome Co. | Pesticidal compounds |
AU604660B2 (en) * | 1985-12-17 | 1991-01-03 | Wellcome Foundation Limited, The | Pesticidal compounds |
GB8628467D0 (en) * | 1986-11-28 | 1987-01-07 | Wellcome Found | Pesticidal compounds |
GB8726735D0 (en) * | 1987-11-14 | 1987-12-16 | Wellcome Found | Pesticidal compounds |
JPH02749A (ja) * | 1988-01-20 | 1990-01-05 | Sumitomo Chem Co Ltd | フルオロジオレフィンアミド類、その製造方法およびそれを有効成分とする殺虫、殺ダニ剤 |
-
1989
- 1989-06-07 DE DE68924199T patent/DE68924199T2/de not_active Expired - Fee Related
- 1989-06-07 EP EP89305773A patent/EP0346107B1/en not_active Expired - Lifetime
- 1989-06-07 AT AT89305773T patent/ATE127790T1/de active
- 1989-06-08 JP JP1146540A patent/JP2667908B2/ja not_active Expired - Lifetime
- 1989-06-08 PT PT90790A patent/PT90790B/pt not_active IP Right Cessation
- 1989-06-08 IL IL90568A patent/IL90568A0/xx unknown
- 1989-06-08 EG EG27989A patent/EG19009A/xx active
- 1989-06-08 NZ NZ229459A patent/NZ229459A/en unknown
- 1989-06-08 HU HU892919A patent/HU207036B/hu not_active IP Right Cessation
- 1989-06-08 FI FI892819A patent/FI892819A/fi not_active Application Discontinuation
- 1989-06-08 AU AU36233/89A patent/AU619853B2/en not_active Ceased
- 1989-06-08 US US07/364,082 patent/US5180737A/en not_active Expired - Fee Related
- 1989-06-08 KR KR1019890007968A patent/KR910000649A/ko not_active Application Discontinuation
- 1989-06-08 DK DK280189A patent/DK280189A/da not_active Application Discontinuation
Also Published As
Publication number | Publication date |
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ATE127790T1 (de) | 1995-09-15 |
HU207036B (en) | 1993-03-01 |
JP2667908B2 (ja) | 1997-10-27 |
IL90568A0 (en) | 1990-01-18 |
JPH0242045A (ja) | 1990-02-13 |
US5180737A (en) | 1993-01-19 |
FI892819A (fi) | 1989-12-10 |
PT90790A (pt) | 1989-12-29 |
EG19009A (en) | 1994-09-29 |
DK280189D0 (da) | 1989-06-08 |
FI892819A0 (fi) | 1989-06-08 |
AU3623389A (en) | 1989-12-14 |
EP0346107B1 (en) | 1995-09-13 |
EP0346107A3 (en) | 1990-12-05 |
EP0346107A2 (en) | 1989-12-13 |
HUT50757A (en) | 1990-03-28 |
PT90790B (pt) | 1994-11-30 |
AU619853B2 (en) | 1992-02-06 |
DE68924199T2 (de) | 1996-02-08 |
NZ229459A (en) | 1992-05-26 |
DK280189A (da) | 1989-12-10 |
DE68924199D1 (de) | 1995-10-19 |
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