JP2599168B2 - 置換されたクロトン酸エステル及び該化合物を含有する殺菌剤 - Google Patents
置換されたクロトン酸エステル及び該化合物を含有する殺菌剤Info
- Publication number
- JP2599168B2 JP2599168B2 JP63035423A JP3542388A JP2599168B2 JP 2599168 B2 JP2599168 B2 JP 2599168B2 JP 63035423 A JP63035423 A JP 63035423A JP 3542388 A JP3542388 A JP 3542388A JP 2599168 B2 JP2599168 B2 JP 2599168B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- methyl
- phenoxy
- benzyloxy
- chloro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000417 fungicide Chemical class 0.000 title claims abstract description 11
- 150000001875 compounds Chemical class 0.000 title claims description 24
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical class C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 title 1
- -1 phenoxy, benzyloxy Chemical group 0.000 claims abstract description 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 5
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 claims abstract description 5
- 125000005677 ethinylene group Chemical group [*:2]C#C[*:1] 0.000 claims abstract description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 241000233866 Fungi Species 0.000 claims description 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims description 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 4
- 230000000855 fungicidal effect Effects 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000005699 methyleneoxy group Chemical group [H]C([H])([*:1])O[*:2] 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
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- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
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- 150000002431 hydrogen Chemical group 0.000 abstract 2
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- CJHXCRMKMMBYJQ-UHFFFAOYSA-N dimethirimol Chemical compound CCCCC1=C(C)NC(N(C)C)=NC1=O CJHXCRMKMMBYJQ-UHFFFAOYSA-N 0.000 description 1
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- 235000013399 edible fruits Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
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- OYRIKLVYHTWHCZ-UHFFFAOYSA-N n-cyclohexyl-2,5-dimethylfuran-3-carboxamide Chemical compound O1C(C)=CC(C(=O)NC2CCCCC2)=C1C OYRIKLVYHTWHCZ-UHFFFAOYSA-N 0.000 description 1
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- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000003431 oxalo group Chemical group 0.000 description 1
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- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
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- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- ILERPRJWJPJZDN-UHFFFAOYSA-N thioquinox Chemical compound C1=CC=C2N=C(SC(=S)S3)C3=NC2=C1 ILERPRJWJPJZDN-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009369 viticulture Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
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Classifications
-
- 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
- A01N37/38—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 having at least one oxygen or sulfur atom attached to an aromatic 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
- 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
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19873705389 DE3705389A1 (de) | 1987-02-20 | 1987-02-20 | Substituierte crotonsaeureester und diese enthaltende fungizide |
| DE3705389.2 | 1987-02-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63222144A JPS63222144A (ja) | 1988-09-16 |
| JP2599168B2 true JP2599168B2 (ja) | 1997-04-09 |
Family
ID=6321382
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63035423A Expired - Fee Related JP2599168B2 (ja) | 1987-02-20 | 1988-02-19 | 置換されたクロトン酸エステル及び該化合物を含有する殺菌剤 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4937372A (cg-RX-API-DMAC7.html) |
| EP (1) | EP0280185B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2599168B2 (cg-RX-API-DMAC7.html) |
| AT (1) | ATE80378T1 (cg-RX-API-DMAC7.html) |
| CA (1) | CA1289969C (cg-RX-API-DMAC7.html) |
| DE (2) | DE3705389A1 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2051779T3 (cg-RX-API-DMAC7.html) |
| GR (1) | GR3005872T3 (cg-RX-API-DMAC7.html) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3811012A1 (de) * | 1988-03-31 | 1989-10-19 | Basf Ag | Ortho-substituierte phenolether und fungizide, die diese verbindungen enthalten |
| JP2512087B2 (ja) * | 1988-06-24 | 1996-07-03 | 株式会社日立製作所 | 光記録媒体および光記録方法 |
| US5286750A (en) * | 1989-10-11 | 1994-02-15 | Basf Aktiengesellschaft | Phenylacetic acid derivatives and fungicides containing them |
| DE4028391A1 (de) * | 1990-09-07 | 1992-03-12 | Basf Ag | (alpha)-arylacrylsaeurederivate, ihre herstellung und verwendung zur bekaempfung von schaedlingen und pilzen |
| US5194622A (en) * | 1990-11-21 | 1993-03-16 | Roussel Uclaf | Process for preparation of thiazolylalkoxy acrylates |
| ES2105903T3 (es) | 1990-12-31 | 1997-10-16 | Basf Ag | Procedimiento para la obtencion de alfa-cetocarboxilatos. |
| DE4105160A1 (de) | 1991-02-20 | 1992-08-27 | Basf Ag | Imino-substiuierte phenylderivate, ihre herstellung und diese enthaltende fungizide |
| DE4116090A1 (de) * | 1991-05-17 | 1992-11-19 | Basf Ag | (alpha)-phenylacrylsaeurederivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen und schadpilzen |
| DE4117371A1 (de) * | 1991-05-28 | 1992-12-03 | Basf Ag | Antimykotische mittel, die phenylessigsaeurederivate enthalten |
| TW224042B (cg-RX-API-DMAC7.html) | 1992-04-04 | 1994-05-21 | Basf Ag | |
| IL106473A0 (en) * | 1992-08-11 | 1993-11-15 | Basf Ag | Acetylene derivatives and crop protection agents containing them |
| IL107690A (en) * | 1992-12-14 | 1997-09-30 | Basf Ag | 2, a-DISUBSTITUTED BENZENEACETOTHIOAMIDES, THEIR PREPARATION AND THEIR USE AS PESTICIDES AND FUNGICIDES |
| IL113414A (en) * | 1994-05-03 | 2000-08-13 | Basf Ag | Substituted methyl alpha-phenylbutenoates their preparation and use for combating harmful fungi and animal pests |
| AU691673B2 (en) * | 1994-11-14 | 1998-05-21 | Dow Agrosciences Llc | Pyridazinones and their use as fungicides |
| DE4442560A1 (de) * | 1994-11-30 | 1996-06-05 | Basf Ag | Iminooxybenzylcrotonsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US5635494A (en) * | 1995-04-21 | 1997-06-03 | Rohm And Haas Company | Dihydropyridazinones and pyridazinones and their use as fungicides and insecticides |
| JPH11504909A (ja) * | 1995-05-04 | 1999-05-11 | ビーエーエスエフ アクチェンゲゼルシャフト | 実質的に異性体として純粋なメチル−ｅ−２−［２−アリールオキシメチレンフェニル］クロトナートの製造方法およびそのための中間生成物 |
| IL118086A0 (en) * | 1995-05-24 | 1996-08-04 | Basf Ag | 2-[2-hetaryloxymethylene phenyl] crotonates their preparation and their use as pesticides |
| EP1118609A3 (de) * | 2000-01-21 | 2002-08-28 | Basf Aktiengesellschaft | Iminooxisubstituierte Benzylphenylether, Verfahren und Zwischenprodukte zu ihrer Herstellung, sie enthaltende Mittel sowie ihre Verwendung zur Bekämpfung von Schadpilzen |
| MXPA05004736A (es) * | 2002-11-12 | 2005-08-02 | Basf Ag | Metodo para mejorar el rendimiento en vegetales resistentes al glifosato. |
| JP5250421B2 (ja) * | 2005-10-28 | 2013-07-31 | ビーエーエスエフ ソシエタス・ヨーロピア | 有害菌類に対する抵抗性を誘導する方法 |
| CA2640963A1 (en) * | 2006-03-14 | 2007-09-20 | Basf Se | Method of inducing tolerance of plants against bacterioses |
| EA015449B1 (ru) * | 2006-03-24 | 2011-08-30 | Басф Се | Способ борьбы с фитопатогенными грибами |
| US20100234366A1 (en) * | 2006-03-29 | 2010-09-16 | Bsf Se | Use of Strobilurins for the Treatment of Disorders of Iron Metabolism |
| CL2008001181A1 (es) | 2007-04-23 | 2009-10-23 | Basf Se | Metodo para mejorar la salud de la planta y/o controlar plagas en plantas con al menos una modificacion transgenica relacionada con el aumento del rendimiento que consiste en la aplicacion de una composicion quimica que comprende al menos un ingrediente activo seleccionado de insecticidas, fungicidas o herbicidas. |
| KR20100039364A (ko) * | 2007-06-29 | 2010-04-15 | 바스프 에스이 | 비생물적 스트레스에 대한 식물의 내성을 증가시키기 위한 스트로빌루린 |
| JP2013500297A (ja) | 2009-07-28 | 2013-01-07 | ビーエーエスエフ ソシエタス・ヨーロピア | 多年生植物の貯蔵組織における遊離アミノ酸レベルを増大させる方法 |
| US20120178625A1 (en) | 2009-09-25 | 2012-07-12 | Basf Se | Method for reducing pistillate flower abortion in plants |
| CN103275009A (zh) * | 2013-06-13 | 2013-09-04 | 南京工业大学 | 一种含芳基甲氧基丙烯酸酯的氯代吡唑类化合物、制备方法及用途 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL275086A (cg-RX-API-DMAC7.html) * | 1961-02-22 | |||
| NZ213630A (en) * | 1984-10-19 | 1990-02-26 | Ici Plc | Acrylic acid derivatives and fungicidal compositions |
| DE3519282A1 (de) * | 1985-05-30 | 1986-12-04 | Basf Ag, 6700 Ludwigshafen | Acrylsaeureester und fungizide, die diese verbindungen enthalten |
-
1987
- 1987-02-20 DE DE19873705389 patent/DE3705389A1/de not_active Withdrawn
-
1988
- 1988-02-08 CA CA000558411A patent/CA1289969C/en not_active Expired - Lifetime
- 1988-02-10 US US07/154,297 patent/US4937372A/en not_active Expired - Lifetime
- 1988-02-18 DE DE8888102331T patent/DE3874365D1/de not_active Expired - Lifetime
- 1988-02-18 EP EP88102331A patent/EP0280185B1/de not_active Expired - Lifetime
- 1988-02-18 AT AT88102331T patent/ATE80378T1/de active
- 1988-02-18 ES ES88102331T patent/ES2051779T3/es not_active Expired - Lifetime
- 1988-02-19 JP JP63035423A patent/JP2599168B2/ja not_active Expired - Fee Related
-
1992
- 1992-10-01 GR GR920402204T patent/GR3005872T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0280185B1 (de) | 1992-09-09 |
| JPS63222144A (ja) | 1988-09-16 |
| DE3705389A1 (de) | 1988-09-01 |
| EP0280185A2 (de) | 1988-08-31 |
| US4937372A (en) | 1990-06-26 |
| ATE80378T1 (de) | 1992-09-15 |
| GR3005872T3 (cg-RX-API-DMAC7.html) | 1993-06-07 |
| DE3874365D1 (de) | 1992-10-15 |
| EP0280185A3 (en) | 1990-06-27 |
| CA1289969C (en) | 1991-10-01 |
| ES2051779T3 (es) | 1994-07-01 |
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