DD248274A5 - Mikrobizides mittel - Google Patents
Mikrobizides mittel Download PDFInfo
- Publication number
- DD248274A5 DD248274A5 DD84281418A DD28141884A DD248274A5 DD 248274 A5 DD248274 A5 DD 248274A5 DD 84281418 A DD84281418 A DD 84281418A DD 28141884 A DD28141884 A DD 28141884A DD 248274 A5 DD248274 A5 DD 248274A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- formula
- plants
- triazol
- chlorophenoxy
- active ingredient
- Prior art date
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- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
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- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
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- 229960000846 camphor Drugs 0.000 description 1
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- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
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- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
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- YZMHQCWXYHARLS-UHFFFAOYSA-N naphthalene-1,2-disulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC=C21 YZMHQCWXYHARLS-UHFFFAOYSA-N 0.000 description 1
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- 239000000376 reactant Substances 0.000 description 1
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- 230000002829 reductive effect Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
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- 238000000926 separation method Methods 0.000 description 1
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- 235000019355 sepiolite Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
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- 235000013619 trace mineral Nutrition 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/178—Unsaturated ethers containing hydroxy or O-metal groups
- C07C43/1782—Unsaturated ethers containing hydroxy or O-metal groups containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Epoxy Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH273083 | 1983-05-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD248274A5 true DD248274A5 (de) | 1987-08-05 |
Family
ID=4240315
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD84281418A DD248274A5 (de) | 1983-05-19 | 1984-05-17 | Mikrobizides mittel |
| DD84263132A DD226882A5 (de) | 1983-05-19 | 1984-05-17 | Verfahren zur herstellung von 1-triazolylethylether-derivaten |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD84263132A DD226882A5 (de) | 1983-05-19 | 1984-05-17 | Verfahren zur herstellung von 1-triazolylethylether-derivaten |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US4945100A (en:Method) |
| EP (1) | EP0126430B1 (en:Method) |
| JP (3) | JPS59222434A (en:Method) |
| KR (2) | KR890000533B1 (en:Method) |
| AT (1) | ATE66676T1 (en:Method) |
| AU (2) | AU572145B2 (en:Method) |
| BR (1) | BR8402388A (en:Method) |
| CA (1) | CA1223264A (en:Method) |
| CS (2) | CS247179B2 (en:Method) |
| DD (2) | DD248274A5 (en:Method) |
| DE (1) | DE3484968D1 (en:Method) |
| DK (1) | DK248184A (en:Method) |
| ES (1) | ES532604A0 (en:Method) |
| GB (2) | GB2143815B (en:Method) |
| GR (1) | GR79954B (en:Method) |
| HU (1) | HU196693B (en:Method) |
| IE (2) | IE57489B1 (en:Method) |
| IL (3) | IL83707A (en:Method) |
| MX (1) | MX5769A (en:Method) |
| MY (1) | MY102774A (en:Method) |
| NZ (2) | NZ208209A (en:Method) |
| PH (3) | PH20959A (en:Method) |
| PT (1) | PT78602A (en:Method) |
| TR (1) | TR22379A (en:Method) |
| ZA (1) | ZA843774B (en:Method) |
Families Citing this family (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0126430B1 (de) * | 1983-05-19 | 1991-08-28 | Ciba-Geigy Ag | Verfahren zur Herstellung von 1-Triazolylethylether-Derivaten, sowie mikrobizide Mittel enthaltende neue 1-triazolyl-phenoxyphenylethylether-derivate als Wirkstoffe und deren Verwendung |
| EP0158448B1 (en) * | 1984-04-05 | 1990-08-29 | Imperial Chemical Industries Plc | Azolyl propanols |
| DE3682023D1 (de) * | 1985-08-07 | 1991-11-21 | Ici Plc | Triazolylmethyl-tert.-butyl-carbinolderivate, verfahren zu ihrer herstellung und ihre verwendung als planzenwachstumsregulatoren. |
| GB8603951D0 (en) * | 1986-02-18 | 1986-03-26 | Ici Plc | Heterocyclic compounds |
| ES2016660B3 (es) * | 1987-01-21 | 1990-11-16 | Ciba-Geigy Ag | Agente microbicida. |
| DE3732387A1 (de) * | 1987-09-25 | 1989-04-06 | Bayer Ag | Azolylmethylcyclopropyl-derivate enthaltende antimykotische mittel |
| DE58903329D1 (de) * | 1988-08-04 | 1993-03-04 | Ciba Geigy Ag | Mikrobizide mittel. |
| US4940720A (en) * | 1989-08-02 | 1990-07-10 | Ciba-Geigy Corporation | Microbicidal compositions |
| US5358939A (en) * | 1992-06-25 | 1994-10-25 | Rohm And Haas Company | Fungicidal 2-aryl-2,2-disubstituted ethyl-1,2,4-triazoles |
| NZ270418A (en) | 1994-02-07 | 1997-09-22 | Eisai Co Ltd | Polycyclic triazole & imidazole derivatives, antifungal compositions |
| KR20020037652A (ko) * | 2000-11-15 | 2002-05-22 | 김응필 | 비중분리 선광기 |
| KR101526016B1 (ko) | 2006-11-22 | 2015-06-04 | 바스프 에스이 | 액체 물 기재 농약 제제 |
| CA2694778A1 (en) | 2007-08-08 | 2009-02-12 | Basf Se | Aqueous microemulsions containing organic insecticide compounds |
| WO2010010005A2 (de) * | 2008-07-24 | 2010-01-28 | Basf Se | Öl-in-wasser emulsion umfassend lösungsmittel, wasser, tensid und pestizid |
| UA106213C2 (ru) | 2008-10-10 | 2014-08-11 | Басф Се | Жидкие препараты для защиты растений, содержащие пираклостробин |
| TW201018400A (en) | 2008-10-10 | 2010-05-16 | Basf Se | Liquid aqueous plant protection formulations |
| CA2840286C (en) | 2011-07-13 | 2016-04-12 | Basf Se | Fungicidal substituted 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds |
| PE20140837A1 (es) * | 2011-07-15 | 2014-07-10 | Basf Se | Compuestos fungicidas 2-[2-cloro-4-(4-cloro-fenoxi)-fenil]-1-[1,2,4]triazol-1-il-etanol alquilo sustituidos |
| CN103814017A (zh) | 2011-07-15 | 2014-05-21 | 巴斯夫欧洲公司 | 杀真菌的苯基烷基取代的2-[2-氯-4-(4-氯苯氧基)苯基]-1-[1,2,4]三唑-1-基乙醇化合物 |
| EP2731934A1 (en) | 2011-07-15 | 2014-05-21 | Basf Se | Fungicidal alkyl- and aryl-substituted 2-[2-chloro-4-(dihalo-phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds |
| EP2744791B1 (en) | 2011-08-15 | 2015-10-28 | Basf Se | Fungicidal substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-alkoxy-3-methyl-butyl}-1h-[1,2,4]triazole compounds |
| AU2012296893A1 (en) | 2011-08-15 | 2014-03-06 | Basf Se | Fungicidal substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-alkoxy-2-alkynyl/alkenyl-ethyl}-1H-[1,2,4]triazole compounds |
| BR112014003412A2 (pt) * | 2011-08-15 | 2017-03-14 | Basf Se | compostos de fórmula i, processo, compostos de fórmula xii, viii e xi, composições agroquímicas, utilização e semente revestida |
| EP2559688A1 (en) | 2011-08-15 | 2013-02-20 | Basf Se | Fungicidal substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-butoxy-ethyl}-1h [1,2,4]triazole compounds |
| US20140162876A1 (en) * | 2011-08-15 | 2014-06-12 | Basf Se | Fungicidal substituted 1--1H-[1,2,4]triazole compounds |
| AR087536A1 (es) | 2011-08-15 | 2014-04-03 | Basf Se | Compuestos fungicidas de 1-{2-[2-halo-4-(4-halogen-fenoxi)-fenil]-2-alquiniloxi-etil}-1h-[1,2,4]triazol sustituidos |
| JP2014524431A (ja) * | 2011-08-15 | 2014-09-22 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌性置換１−｛２−［２−ハロ−４−（４−ハロゲン−フェノキシ）−フェニル］−２−アルコキシ−ヘキシル｝−１ｈ−［１，２，４］トリアゾール化合物 |
| WO2013024080A1 (en) | 2011-08-15 | 2013-02-21 | Basf Se | Fungicidal substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl ]-2-alkoxy-2-cyclyl-ethyl}-1h [1,2,4]triazole compounds |
| US20140308162A1 (en) | 2013-04-15 | 2014-10-16 | Ecolab Usa Inc. | Peroxycarboxylic acid based sanitizing rinse additives for use in ware washing |
| US9752105B2 (en) | 2012-09-13 | 2017-09-05 | Ecolab Usa Inc. | Two step method of cleaning, sanitizing, and rinsing a surface |
| WO2014082879A1 (en) | 2012-11-27 | 2014-06-05 | Basf Se | Substituted [1,2,4]triazole compounds |
| US20150284344A1 (en) * | 2012-11-27 | 2015-10-08 | Basf Se | Substituted [1,2,4]triazole Compounds |
| WO2014082871A1 (en) | 2012-11-27 | 2014-06-05 | Basf Se | Substituted 2-[phenoxy-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds and their use as fungicides |
| US20160029630A1 (en) | 2012-11-27 | 2016-02-04 | Basf Se | Substituted 2-[phenoxy-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds and their use as fungicides |
| US20150313229A1 (en) | 2012-11-27 | 2015-11-05 | Basf Se | Substituted [1,2,4] Triazole Compounds |
| EP2735563A1 (en) * | 2012-11-27 | 2014-05-28 | Basf Se | Meta substituted 2-[phenoxy-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds and their use as fungicides |
| BR112015014583B1 (pt) * | 2012-12-19 | 2020-04-28 | Basf Se | compostos, processo para a preparação de compostos, compostos intermediários, composição, usos de um composto de fórmula i e método para combater fungos nocivos |
| CN104936450A (zh) * | 2012-12-20 | 2015-09-23 | 巴斯夫欧洲公司 | 包含三唑化合物的组合物 |
| MX377401B (es) * | 2012-12-20 | 2025-03-07 | Basf Agro Bv | Composiciones que comprenden un compuesto de triazol. |
| EP2943486A1 (en) * | 2013-01-09 | 2015-11-18 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| CN104968651A (zh) | 2013-01-09 | 2015-10-07 | 巴斯夫农业公司 | 制备取代环氧乙烷类和三唑类的方法 |
| WO2014124850A1 (en) | 2013-02-14 | 2014-08-21 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| WO2014198553A1 (en) * | 2013-06-12 | 2014-12-18 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| EP2813499A1 (en) | 2013-06-12 | 2014-12-17 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| WO2014198557A1 (en) * | 2013-06-12 | 2014-12-18 | Basf Se | Substituted [1,2,4]triazole and imidazole compounds |
| PL3019013T3 (pl) * | 2013-07-08 | 2021-10-25 | BASF Agro B.V. | Kompozycje zawierające związek triazolowy i biopestycyd |
| EP2839745A1 (en) | 2013-08-21 | 2015-02-25 | Basf Se | Agrochemical formulations comprising a 2-ethyl-hexanol alkoxylate |
| JP6053948B2 (ja) | 2013-10-24 | 2016-12-27 | 三菱電機株式会社 | 情報処理装置及び情報処理方法及びプログラム |
| BR112016018522B1 (pt) | 2014-02-14 | 2021-05-18 | BASF Agro B.V. | concentrado emulsionável, processo para preparar o concentrado, emulsão e método para controlar fungos fitopatogênicos |
| US10212934B2 (en) * | 2014-06-25 | 2019-02-26 | BASF Agro B.V. | Pesticidal compositions |
| US10053436B2 (en) | 2014-07-08 | 2018-08-21 | BASF Agro B.V. | Process for the preparation of substituted oxiranes and triazoles |
| BR112016030281B1 (pt) | 2014-07-14 | 2022-02-15 | Basf Se | Composições, uso de uma composição, método para o combate dos fungos fitopatogênicos e sementes revestidas |
| WO2016071167A1 (en) | 2014-11-07 | 2016-05-12 | Basf Se | Pesticidal mixtures |
| EP3028573A1 (en) | 2014-12-05 | 2016-06-08 | Basf Se | Use of a triazole fungicide on transgenic plants |
| WO2016174042A1 (en) | 2015-04-27 | 2016-11-03 | BASF Agro B.V. | Pesticidal compositions |
| DK3294700T3 (da) | 2015-05-08 | 2020-04-14 | Basf Agro Bv | Fremgangsmåde til fremstilling af limonen-4-ol |
| DK3294720T3 (da) | 2015-05-08 | 2021-02-15 | Basf Agro Bv | Fremgangsmåde til fremstilling af terpinolenepoxid |
| EP3111763A1 (en) | 2015-07-02 | 2017-01-04 | BASF Agro B.V. | Pesticidal compositions comprising a triazole compound |
| WO2017001252A1 (en) | 2015-07-02 | 2017-01-05 | BASF Agro B.V. | Pesticidal compositions comprising a triazole compound |
| JP6903074B2 (ja) | 2016-03-16 | 2021-07-14 | ビーエイエスエフ・ソシエタス・エウロパエアＢａｓｆ Ｓｅ | 穀類につく耐性植物病原菌類を駆除するためのテトラゾリノンの使用 |
| US11241012B2 (en) | 2016-03-16 | 2022-02-08 | Basf Se | Use of tetrazolinones for combating resistant phytopathogenic fungi on soybean |
| CA3015456A1 (en) | 2016-03-16 | 2017-09-21 | Basf Se | Use of tetrazolinones for combating resistant phytopathogenic fungi on fruits |
| KR20190017924A (ko) | 2016-06-15 | 2019-02-20 | 바스프 아그로 비.브이. | 4치환 알켄의 에폭시화 방법 |
| CN109311836A (zh) | 2016-06-15 | 2019-02-05 | 巴斯夫农业公司 | 环氧化四取代烯烃的方法 |
| CN109715622A (zh) | 2016-09-22 | 2019-05-03 | 拜耳作物科学股份公司 | 新的三唑衍生物及其作为杀真菌剂的用途 |
| CN109715621A (zh) | 2016-09-22 | 2019-05-03 | 拜耳作物科学股份公司 | 新的三唑衍生物 |
| BR112019016240A2 (pt) | 2017-02-08 | 2020-04-07 | Bayer Ag | derivados de triazoletiona |
| EP3580218A1 (en) | 2017-02-08 | 2019-12-18 | Bayer CropScience Aktiengesellschaft | Novel triazole derivatives |
| BR112019016241A2 (pt) | 2017-02-08 | 2020-04-07 | Bayer Cropscience Ag | derivados de triazol e seu uso como fungicidas |
| CN110300522A (zh) | 2017-02-10 | 2019-10-01 | 拜耳公司 | 用于防治有害微生物的包含1-(苯氧基-吡啶基)-2-(1,2,4-三唑-1-基)-乙醇衍生物的组合物 |
| EP3421460A1 (en) | 2018-03-15 | 2019-01-02 | Bayer Aktiengesellschaft | 2-[(4-alkylphenoxy)-pyridinyl]-1-(1,2,4-triazol-1-yl)alkan-2-ol fungicides |
| WO2020020813A1 (en) | 2018-07-25 | 2020-01-30 | Bayer Aktiengesellschaft | Fungicidal active compound combinations |
| WO2020020816A1 (en) | 2018-07-26 | 2020-01-30 | Bayer Aktiengesellschaft | Novel triazole derivatives |
| WO2020070050A1 (en) | 2018-10-01 | 2020-04-09 | Bayer Aktiengesellschaft | Fungicidal 5-substituted imidazol-1-yl carbinol derivatives |
| EP3620053A1 (en) | 2018-12-14 | 2020-03-11 | Bayer Aktiengesellschaft | Fungicidal active compound combinations |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2547953A1 (de) * | 1975-10-27 | 1977-04-28 | Bayer Ag | (1-phenyl-2-triazolyl-aethyl)-aether- derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| AU515134B2 (en) * | 1976-08-10 | 1981-03-19 | Janssen Pharmaceutica N.V. | 1-(2-aryl-2-r-ethyl)-1h-1,2,4-triazoles |
| DE2650831A1 (de) * | 1976-11-06 | 1978-05-11 | Basf Ag | Mittel zur beeinflussung des pflanzenwachstums |
| DE2725214A1 (de) * | 1977-06-03 | 1978-12-14 | Bayer Ag | Metallsalzkomplexe von 1-phenyl-2- triazolyl-aethyl-derivaten, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
| DE2725314A1 (de) * | 1977-06-04 | 1978-12-14 | Bayer Ag | 1-(2-phenylaethyl)-triazolium-salze, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
| US4654332A (en) * | 1979-03-07 | 1987-03-31 | Imperial Chemical Industries Plc | Heterocyclic compounds |
| CH647513A5 (de) * | 1979-11-13 | 1985-01-31 | Sandoz Ag | Triazol-derivate, deren herstellung und verwendung. |
| AU542623B2 (en) * | 1980-05-16 | 1985-02-28 | Bayer Aktiengesellschaft | 1-hydroxyethyl-azole derivatives |
| AU546200B2 (en) * | 1980-08-18 | 1985-08-22 | Imperial Chemical Industries Plc | Mono-n-substituted 1,2,4-triazoles |
| DE3175673D1 (en) * | 1980-11-19 | 1987-01-15 | Ici Plc | Triazole compounds, a process for preparing them, their use as plant fungicides and fungicidal compositions containing them |
| DE3140276A1 (de) * | 1981-10-10 | 1983-04-28 | Bayer Ag, 5090 Leverkusen | Phenoxyphenyl-azolylmethyl-ketone und -carbinole, verfahren zu ihrer herstellung und ihre verwendung als fungizide und als zwischenprodukte |
| GB2110684B (en) * | 1981-11-27 | 1985-11-06 | Ciba Geigy Ag | Substituted azolyl-ethyl ethers amd microbicidal compositions thereof |
| DE3202604A1 (de) * | 1982-01-27 | 1983-08-04 | Bayer Ag, 5090 Leverkusen | Ether-derivate von substituierten 1-hydroxyalkyl-azolen, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide und pflanzenwachstumsregulatoren |
| US4610716A (en) * | 1982-12-14 | 1986-09-09 | Ciba-Geigy Corporation | Fluorinated azolyl ethanol growth regulators and microbicides |
| EP0126430B1 (de) * | 1983-05-19 | 1991-08-28 | Ciba-Geigy Ag | Verfahren zur Herstellung von 1-Triazolylethylether-Derivaten, sowie mikrobizide Mittel enthaltende neue 1-triazolyl-phenoxyphenylethylether-derivate als Wirkstoffe und deren Verwendung |
-
1984
- 1984-05-16 EP EP84105582A patent/EP0126430B1/de not_active Expired - Lifetime
- 1984-05-16 AT AT84105582T patent/ATE66676T1/de active
- 1984-05-16 GB GB08412506A patent/GB2143815B/en not_active Expired
- 1984-05-16 DE DE8484105582T patent/DE3484968D1/de not_active Expired - Lifetime
- 1984-05-17 CA CA000454548A patent/CA1223264A/en not_active Expired
- 1984-05-17 GR GR74745A patent/GR79954B/el unknown
- 1984-05-17 PT PT78602A patent/PT78602A/pt not_active IP Right Cessation
- 1984-05-17 DD DD84281418A patent/DD248274A5/de not_active IP Right Cessation
- 1984-05-17 IL IL8483707A patent/IL83707A/xx unknown
- 1984-05-17 IL IL71862A patent/IL71862A/xx unknown
- 1984-05-17 DK DK248184A patent/DK248184A/da not_active Application Discontinuation
- 1984-05-17 DD DD84263132A patent/DD226882A5/de not_active IP Right Cessation
- 1984-05-18 ZA ZA843774A patent/ZA843774B/xx unknown
- 1984-05-18 HU HU841926A patent/HU196693B/hu not_active IP Right Cessation
- 1984-05-18 NZ NZ208209A patent/NZ208209A/en unknown
- 1984-05-18 ES ES532604A patent/ES532604A0/es active Granted
- 1984-05-18 IE IE2779/88A patent/IE57489B1/en not_active IP Right Cessation
- 1984-05-18 NZ NZ219282A patent/NZ219282A/en unknown
- 1984-05-18 CS CS843769A patent/CS247179B2/cs unknown
- 1984-05-18 AU AU28358/84A patent/AU572145B2/en not_active Ceased
- 1984-05-18 IE IE1247/84A patent/IE57488B1/en not_active IP Right Cessation
- 1984-05-18 TR TR3611/84A patent/TR22379A/xx unknown
- 1984-05-18 BR BR8402388A patent/BR8402388A/pt not_active IP Right Cessation
- 1984-05-18 MX MX576984A patent/MX5769A/es unknown
- 1984-05-18 PH PH30696A patent/PH20959A/en unknown
- 1984-05-19 JP JP59101625A patent/JPS59222434A/ja active Granted
- 1984-05-19 KR KR1019840002741A patent/KR890000533B1/ko not_active Expired
-
1985
- 1985-08-08 CS CS855782A patent/CS247200B2/cs unknown
- 1985-10-25 PH PH32974A patent/PH22876A/en unknown
- 1985-10-25 PH PH32973A patent/PH21667A/en unknown
-
1986
- 1986-09-22 GB GB08622763A patent/GB2179659B/en not_active Expired
-
1987
- 1987-08-31 IL IL83707A patent/IL83707A0/xx unknown
- 1987-09-30 MY MYPI87002496A patent/MY102774A/en unknown
-
1988
- 1988-05-02 AU AU15504/88A patent/AU607993B2/en not_active Ceased
- 1988-09-02 US US07/240,441 patent/US4945100A/en not_active Expired - Fee Related
- 1988-11-10 KR KR1019880014855A patent/KR900003367B1/ko not_active Expired
-
1989
- 1989-05-01 JP JP1112793A patent/JPH0296544A/ja active Granted
- 1989-05-01 JP JP1112794A patent/JPH0285265A/ja active Granted
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