KR960000864A - 에스테르 화합물 및 활성 성분으로서 이를 함유하는 해충 억제제 - Google Patents
에스테르 화합물 및 활성 성분으로서 이를 함유하는 해충 억제제 Download PDFInfo
- Publication number
- KR960000864A KR960000864A KR1019950016074A KR19950016074A KR960000864A KR 960000864 A KR960000864 A KR 960000864A KR 1019950016074 A KR1019950016074 A KR 1019950016074A KR 19950016074 A KR19950016074 A KR 19950016074A KR 960000864 A KR960000864 A KR 960000864A
- Authority
- KR
- South Korea
- Prior art keywords
- dimethylmaleimidomethyl
- dimethyl
- cyclopropane
- ethenyl
- carboxylate
- Prior art date
Links
- -1 Ester Compounds Chemical class 0.000 title claims abstract 17
- 241000607479 Yersinia pestis Species 0.000 title claims abstract 6
- 239000004480 active ingredient Substances 0.000 title claims abstract 4
- 239000003112 inhibitor Substances 0.000 title claims abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract 3
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract 3
- 125000005843 halogen group Chemical group 0.000 claims abstract 3
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims 1
- PHMLUXKDHHLSQX-YNKURJBOSA-N 2-(2,5-dioxopyrrol-1-yl)propan-2-yl (1r,3r)-3-[(e)-3-ethoxy-2-fluoro-3-oxoprop-1-enyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](\C=C(\F)C(=O)OCC)[C@H]1C(=O)OC(C)(C)N1C(=O)C=CC1=O PHMLUXKDHHLSQX-YNKURJBOSA-N 0.000 claims 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- GGNIURZZDOJNBN-AATRIKPKSA-N C/C(=C\OC(=O)C1CC1)/C(=O)OC Chemical compound C/C(=C\OC(=O)C1CC1)/C(=O)OC GGNIURZZDOJNBN-AATRIKPKSA-N 0.000 claims 1
- QDONIOOEYUSGFU-WAYWQWQTSA-N C1(CC1)C(=O)O\C=C/C(=O)OCC Chemical compound C1(CC1)C(=O)O\C=C/C(=O)OCC QDONIOOEYUSGFU-WAYWQWQTSA-N 0.000 claims 1
- NNUIBHUOKCVRSW-VMPITWQZSA-N C1CC1C(=O)O/C=C(\C(=O)OC2CC2)/F Chemical compound C1CC1C(=O)O/C=C(\C(=O)OC2CC2)/F NNUIBHUOKCVRSW-VMPITWQZSA-N 0.000 claims 1
- FJVNHIVWSMSLAH-ZZXKWVIFSA-N C1CC1C(=O)O/C=C(\C(=O)OCC(F)(F)F)/F Chemical class C1CC1C(=O)O/C=C(\C(=O)OCC(F)(F)F)/F FJVNHIVWSMSLAH-ZZXKWVIFSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Chemical group 0.000 claims 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 239000012024 dehydrating agents Substances 0.000 claims 1
- 239000011737 fluorine Chemical group 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 150000007530 organic bases Chemical class 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/44—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
- C07D207/444—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
- C07D207/448—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. maleimide
- C07D207/452—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. maleimide with hydrocarbon radicals, substituted by hetero atoms, directly attached to the ring nitrogen 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
- A01N43/08—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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Abstract
탁월한 해충 억제 효과를 나타내는 하기 일반식(I)의 에스테르 화합물, 활성 성분으로서 이를 함유하는 억제제 및 이의 제조 방법.
(상기 식에서 X는 할로겐 원자, 수소 원자 도는 메틸기를 나타내고, R은 알킬, 시클로알킬 또는 할로알킬기를 나타낸다.)
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (13)
- 하기 일반식(I)의 에스테르 화합물 :(상기 식에서 X는 할로겐 원자, 수소 원자 도는 메틸기를 나타내고, R은 알킬, 시클로알킬 또는 할로알킬기를 나타낸다.)
- 제1항에 있어서, X가 수소, 불소, 염소, 브롬 원자 또는 메틸기이고, R이 C1-C5알킬, C3-C5시클로알킬 또는 C1-C5할로알킬기인 에스테르 화합물.
- 제1항에 있어서,X가 수소 또는 불소 원자이고, R이 C1-C3알킬, 시클로프로필 또는 C1-C3할로알킬기인 에스테르 화합물.
- 디메틸말레이미도메틸(1R, 시스)-2,2-디메틸-3(E)-[2-플루오르-2-(에톡시카르보닐)에테닐]시클로프로판-1-카르복실레이트.
- 디메틸말레이미도메틸(1R, 시스)-2,2-디메틸-3(E)-[2-플루오르-2-(시클로프로필옥시카르보닐)에테닐]시클로프로판-1-카르복실레이트.
- 디메틸말레이미도메틸(1R, 시스)-2,2-디메틸-3(E)-[2-플루오르-2-(2,2,2-트리플루오로에톡시카르보닐)에테닐]시클로프로판-1-카르복실레이트.
- 디메틸말레이미도메틸(1R, 시스)-2,2-디메틸-3(Z)-[2-(에톡시카르보닐)에테닐]시클로프로판-1-카르복실레이트.
- 디메틸말레이미도메틸(1R, 시스)-2,2-디메틸-3(Z)-[2-(1,1,1,3,3,3-헥사플루오로이소프로필옥시카르보닐)에테닐]시클로프로판-1-카르복실레이트.
- 디메틸말레이미도메틸(1R, 트란스)-2,2-디메틸-3(E)-[2-(메톡시카르보닐)프로페닐]시클로프로판-1-카르복실레이트.
- 비활성 담체를 포함하고 하기 일반식(I)의 에스테르 화합물을 활성 성분으로서 함유하는 해충 억제제:(상기 식에서 X는 할로겐 원자, 수소 원자 도는 메틸기를 나타내고, R은 알킬, 시클로알킬 또는 할로알킬기를 나타낸다.)
- 하기식(Ⅲ)의 알콜 화합물을, 탈수제 존재하에서 하기식(Ⅱ)의 카르복실산 화합물과 반응시키기거나 유기염기의 존재하에서 하기식(Ⅱ)의 카르복실산 화합물의 산 염화물과 반응시킴을 특징으로 하는, 제1항에서 청구된 식(I)의 에스테르 화합물의 제조방법.(상기 식에서, X및 R은 제1항에서 정의된 바와 같다)
- 제1항에서 청구된 에스테르 화합물의 유효량을 해충이 번식하는 장소에 살포함을 특징으로 하는 해충의 억제 방법.
- 해충 억제를 위해 활성 성분으로서 사용됨을 특징으로 하는 제1항에서 청구된 에스테르 화합물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP94-136051 | 1994-06-17 | ||
JP13605194 | 1994-06-17 | ||
JP11041595A JP3694915B2 (ja) | 1994-06-17 | 1995-05-09 | エステル化合物およびそれを有効成分とする有害生物防除剤 |
JP95-110415 | 1995-05-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR960000864A true KR960000864A (ko) | 1996-01-25 |
Family
ID=26450050
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019950016074A KR960000864A (ko) | 1994-06-17 | 1995-06-16 | 에스테르 화합물 및 활성 성분으로서 이를 함유하는 해충 억제제 |
Country Status (12)
Country | Link |
---|---|
US (1) | US5607963A (ko) |
EP (2) | EP0924200B1 (ko) |
JP (1) | JP3694915B2 (ko) |
KR (1) | KR960000864A (ko) |
CN (1) | CN1059670C (ko) |
AU (1) | AU685610B2 (ko) |
BR (1) | BR9502835A (ko) |
CA (1) | CA2150501A1 (ko) |
DE (2) | DE69525777D1 (ko) |
ES (2) | ES2144069T3 (ko) |
PT (1) | PT691330E (ko) |
TW (1) | TW340788B (ko) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19626469A1 (de) * | 1996-07-02 | 1998-01-08 | Bayer Ag | Neue insektizide Formulierungen |
JP5066843B2 (ja) * | 2006-06-15 | 2012-11-07 | 住友化学株式会社 | エステル化合物及びその有害生物防除用途 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1434956A (fr) * | 1963-04-11 | 1966-04-15 | Sumitomo Chemical Co | Esters cyclopropane-carboxyliques |
NL125058C (ko) * | 1963-04-11 | |||
AU432259B1 (en) * | 1970-02-26 | 1972-08-24 | Sumitomo Chemical Company, Limited | Novel substituted chrysanthemates |
US3867542A (en) * | 1970-02-26 | 1975-02-18 | Sumitomo Chemical Co | Certain substituted chrysanthemates as insecticides |
DE2113124C3 (de) * | 1970-03-19 | 1974-07-04 | Sumitomo Chemical Co., Ltd., Osaka (Japan) | Cyclopropancarbonsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide |
US3847944A (en) * | 1970-12-25 | 1974-11-12 | Sumitomo Chemical Co | Propenylcyclopropanecarboxylates |
OA06786A (fr) | 1980-04-16 | 1982-12-31 | Roussel Uclaf | Nouveaux dérivés de l'acide cyclopropane, leur préparation, leur application à la lutte contre les parasites des végétaux et des animaux, les compositions les renfermant et les nouveaux intermediaires obtenus. |
FR2486073A1 (fr) | 1980-07-02 | 1982-01-08 | Roussel Uclaf | Nouveaux derives de l'acide cyclopropane carboxylique, leur procede de preparation, et leur application a la lutte contre les parasites |
FR2491060A1 (fr) * | 1980-10-01 | 1982-04-02 | Roussel Uclaf | Esters d'acides cyclopropanes carboxyliques apparentes a l'acide pyrethrique, leur procede de preparation et leur application a la lutte contre les parasites |
EP0183111B1 (de) | 1984-11-26 | 1988-01-07 | Werkzeugmaschinenfabrik Oerlikon-Bührle AG | Schalt- oder Steuerkabel |
FR2678611B1 (fr) * | 1991-07-04 | 1995-01-20 | Roussel Uclaf | Nouveaux esters pyrethrinouides de l'alcool 1,3,4,5,6,7-hexahydro 1,3-dioxo-2h-isoindol-2-yl-methylique, leur procede de preparation et leur application comme pesticides. |
-
1995
- 1995-05-09 JP JP11041595A patent/JP3694915B2/ja not_active Expired - Fee Related
- 1995-05-29 AU AU20327/95A patent/AU685610B2/en not_active Ceased
- 1995-05-30 CA CA002150501A patent/CA2150501A1/en not_active Abandoned
- 1995-06-01 US US08/456,309 patent/US5607963A/en not_active Expired - Lifetime
- 1995-06-10 TW TW084105931A patent/TW340788B/zh active
- 1995-06-14 DE DE69525777T patent/DE69525777D1/de not_active Expired - Lifetime
- 1995-06-14 DE DE69515936T patent/DE69515936T2/de not_active Expired - Fee Related
- 1995-06-14 ES ES95109224T patent/ES2144069T3/es not_active Expired - Lifetime
- 1995-06-14 EP EP99101528A patent/EP0924200B1/en not_active Expired - Lifetime
- 1995-06-14 EP EP95109224A patent/EP0691330B1/en not_active Expired - Lifetime
- 1995-06-14 ES ES99101528T patent/ES2170550T3/es not_active Expired - Lifetime
- 1995-06-14 PT PT95109224T patent/PT691330E/pt unknown
- 1995-06-16 KR KR1019950016074A patent/KR960000864A/ko active IP Right Grant
- 1995-06-16 CN CN95107054A patent/CN1059670C/zh not_active Expired - Lifetime
- 1995-06-16 BR BR9502835A patent/BR9502835A/pt not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE69515936T2 (de) | 2000-08-17 |
BR9502835A (pt) | 1996-03-12 |
PT691330E (pt) | 2000-07-31 |
TW340788B (en) | 1998-09-21 |
EP0691330A1 (en) | 1996-01-10 |
EP0924200A1 (en) | 1999-06-23 |
DE69515936D1 (de) | 2000-05-04 |
US5607963A (en) | 1997-03-04 |
EP0924200B1 (en) | 2002-03-06 |
AU685610B2 (en) | 1998-01-22 |
JP3694915B2 (ja) | 2005-09-14 |
EP0691330B1 (en) | 2000-03-29 |
AU2032795A (en) | 1996-01-04 |
DE69525777D1 (de) | 2002-04-11 |
CN1121511A (zh) | 1996-05-01 |
JPH0859613A (ja) | 1996-03-05 |
ES2170550T3 (es) | 2002-08-01 |
CN1059670C (zh) | 2000-12-20 |
ES2144069T3 (es) | 2000-06-01 |
CA2150501A1 (en) | 1995-12-18 |
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