RU2091024C1 - Почвенная фунгицидная композиция, способ защиты растений, дигидрат кальциевой соли 3-гидрокси-5-метилизоксазола, способ его получения, фунгицидная композиция и способ защиты растений - Google Patents
Почвенная фунгицидная композиция, способ защиты растений, дигидрат кальциевой соли 3-гидрокси-5-метилизоксазола, способ его получения, фунгицидная композиция и способ защиты растений Download PDFInfo
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- RU2091024C1 RU2091024C1 RU93005331/04A RU93005331A RU2091024C1 RU 2091024 C1 RU2091024 C1 RU 2091024C1 RU 93005331/04 A RU93005331/04 A RU 93005331/04A RU 93005331 A RU93005331 A RU 93005331A RU 2091024 C1 RU2091024 C1 RU 2091024C1
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- Prior art keywords
- hydroxy
- methylisoxazole
- weight
- parts
- salt
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- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
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Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members 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
- C07D261/12—Oxygen 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
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| JP4-114808 | 1992-05-07 | ||
| JP11480892 | 1992-05-07 | ||
| JP4252393 | 1993-03-03 | ||
| JP5-42523 | 1993-03-03 | ||
| JP4-42523 | 1993-03-03 |
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| RU93005331A RU93005331A (ru) | 1996-04-27 |
| RU2091024C1 true RU2091024C1 (ru) | 1997-09-27 |
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| RU93005331/04A RU2091024C1 (ru) | 1992-05-07 | 1993-05-06 | Почвенная фунгицидная композиция, способ защиты растений, дигидрат кальциевой соли 3-гидрокси-5-метилизоксазола, способ его получения, фунгицидная композиция и способ защиты растений |
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| EP (1) | EP0569210B1 (enExample) |
| KR (1) | KR100278876B1 (enExample) |
| CN (2) | CN1070022C (enExample) |
| AT (1) | ATE162046T1 (enExample) |
| CA (1) | CA2095658C (enExample) |
| CZ (1) | CZ287192B6 (enExample) |
| DE (1) | DE69316262T2 (enExample) |
| DK (1) | DK0569210T3 (enExample) |
| EE (1) | EE03133B1 (enExample) |
| ES (1) | ES2114001T3 (enExample) |
| FI (1) | FI106525B (enExample) |
| GR (1) | GR3026360T3 (enExample) |
| HU (1) | HU215381B (enExample) |
| IL (1) | IL105577A (enExample) |
| LT (1) | LT3180B (enExample) |
| LV (1) | LV10447B (enExample) |
| PL (2) | PL172320B1 (enExample) |
| RU (1) | RU2091024C1 (enExample) |
| SK (1) | SK280972B6 (enExample) |
| TW (1) | TW272115B (enExample) |
| UY (1) | UY23579A1 (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005104852A1 (fr) * | 2004-04-29 | 2005-11-10 | Zakrytoe Aktsionernoe Obschestvo 'institut Sistemnyx Innovaciy 'salus' | Preparation fongicide universelle 'donor' |
| RU2269264C2 (ru) * | 2000-08-31 | 2006-02-10 | Тор Гмбх | Композиция для борьбы с микроорганизмами, ее применение для борьбы с вредными микроорганизмами |
| WO2011084085A1 (ru) * | 2010-01-11 | 2011-07-14 | Mokhov Victor Valentinovich | Биоорганический препарат для обработки растений (варианты) |
| RU2658990C2 (ru) * | 2012-12-31 | 2018-06-26 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Композиции и способы для модулирования скорости образования ebis из дитиокарбаматных фунгицидов |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2174484A1 (en) * | 1995-04-20 | 1996-10-21 | Masaki Hashimoto | Cut flower preservative slurry composition |
| AU7728498A (en) * | 1997-06-09 | 1998-12-30 | Dustin Investments Cc | A composition for use as a pharmaceutical and in specific agricultural and industrial applications |
| KR100649731B1 (ko) * | 1998-11-06 | 2006-11-24 | 메비올 가부시키가이샤 | 식물 보수용 담체 및 식물체 육성용 보수재 |
| JP3182648B2 (ja) * | 1999-05-12 | 2001-07-03 | ティーディーケイ株式会社 | セラミック成形体の成形用のセラミック顆粒、その製造または処理方法、セラミック成形体およびその製造方法 |
| DE10001548A1 (de) * | 2000-01-14 | 2001-07-19 | Innovation Pro Terra Gmbh & Co | Pflanzsubstrate |
| US7977119B2 (en) * | 2004-12-08 | 2011-07-12 | Agilent Technologies, Inc. | Chemical arrays and methods of using the same |
| US20070207927A1 (en) * | 2006-03-01 | 2007-09-06 | Rosa Fred C | Polymer based seed coating |
| BR112013019287B1 (pt) * | 2011-01-28 | 2019-08-06 | Deepak Pranjivandas Shah | Composição pesticida contendo enxofre |
| CN102516190B (zh) * | 2011-12-06 | 2014-04-09 | 西北农林科技大学 | 噁唑喹啉类有机铜化合物及其制备方法、制剂及在防治农业植物病害中的用途 |
| CN102516189B (zh) * | 2011-12-06 | 2014-04-09 | 西北农林科技大学 | 噁唑类有机铜化合物及其制备方法、制剂及在防治农业植物病害中的用途 |
| EP3954215A4 (en) * | 2019-04-05 | 2023-01-04 | Mitsui Chemicals Agro, Inc. | AGROCHEMICAL COMPOSITION WITH ENHANCED EFFICIENCY |
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|---|---|---|---|---|
| NL130992C (enExample) | 1964-09-14 | |||
| GB1199737A (en) * | 1967-08-18 | 1970-07-22 | Sankyo Co | Process for the preparation of 3-Hydroxyisoxazole Compounds and Alkali Metal Salts thereof |
| GB1256835A (enExample) * | 1969-07-03 | 1971-12-15 | ||
| JPS4838148B1 (enExample) * | 1970-05-07 | 1973-11-15 | ||
| JPS4940933B1 (enExample) * | 1970-08-19 | 1974-11-06 | ||
| JPS4838148A (enExample) * | 1971-09-10 | 1973-06-05 | ||
| JPS5710083B2 (enExample) * | 1972-04-25 | 1982-02-24 | ||
| JPS4922821A (enExample) * | 1972-06-20 | 1974-02-28 | ||
| JPS5430097B2 (enExample) * | 1972-06-29 | 1979-09-28 | ||
| JPS4940933A (enExample) * | 1972-08-25 | 1974-04-17 | ||
| JPS5679605A (en) * | 1979-12-04 | 1981-06-30 | Sankyo Co Ltd | Preventing agent against damping-off of rice plant |
| JPS5687506A (en) * | 1979-12-19 | 1981-07-16 | Sankyo Co Ltd | Preventing agent against damping-off of rice plant |
| CA1264566A (en) * | 1984-09-05 | 1990-01-23 | Tetsuji Iwasaki | Biocidal fine powder, its manufacturing method and a suspension for agricultural use containing the above powder |
| JPS61151650A (ja) * | 1984-12-26 | 1986-07-10 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀カラ−写真感光材料の処理方法 |
| DE3609939A1 (de) * | 1986-03-24 | 1987-10-01 | Cassella Ag | Fluessige zubereitung von 1,2-benzisothiazolin-3-on, ihre herstellung und verwendung |
| US5219875A (en) * | 1990-11-27 | 1993-06-15 | Rohm And Haas Company | Antimicrobial compositions comprising iodopropargyl butylcarbamate and 1,2-benzisothiazolin-3-one and methods of controlling microbes |
| JPH05108798A (ja) | 1991-10-17 | 1993-04-30 | Shinko Electric Ind Co Ltd | 画像処理方法と画像処理装置 |
| JP4538953B2 (ja) | 1997-12-26 | 2010-09-08 | 日本ゼオン株式会社 | −ch2−chf−基を有する化合物の製造方法 |
| JP4529263B2 (ja) | 2000-09-18 | 2010-08-25 | 沖電気工業株式会社 | アイリス認識装置 |
| JP3973380B2 (ja) | 2001-07-25 | 2007-09-12 | シャープ株式会社 | 液晶表示装置 |
| JP4572625B2 (ja) | 2004-08-25 | 2010-11-04 | 三菱マテリアルシ−エムアイ株式会社 | モータ |
-
1993
- 1993-04-30 IL IL105577A patent/IL105577A/xx not_active IP Right Cessation
- 1993-05-03 LT LTIP508A patent/LT3180B/lt unknown
- 1993-05-04 DE DE69316262T patent/DE69316262T2/de not_active Expired - Fee Related
- 1993-05-04 ES ES93303446T patent/ES2114001T3/es not_active Expired - Lifetime
- 1993-05-04 AT AT93303446T patent/ATE162046T1/de not_active IP Right Cessation
- 1993-05-04 DK DK93303446T patent/DK0569210T3/da active
- 1993-05-04 EP EP93303446A patent/EP0569210B1/en not_active Expired - Lifetime
- 1993-05-04 TW TW082103499A patent/TW272115B/zh active
- 1993-05-06 PL PL93315290A patent/PL172320B1/pl not_active IP Right Cessation
- 1993-05-06 UY UY23579A patent/UY23579A1/es not_active IP Right Cessation
- 1993-05-06 PL PL93298838A patent/PL171674B1/pl not_active IP Right Cessation
- 1993-05-06 CA CA002095658A patent/CA2095658C/en not_active Expired - Fee Related
- 1993-05-06 RU RU93005331/04A patent/RU2091024C1/ru not_active IP Right Cessation
- 1993-05-06 HU HU9301315A patent/HU215381B/hu not_active IP Right Cessation
- 1993-05-07 CN CN93107075A patent/CN1070022C/zh not_active Expired - Fee Related
- 1993-05-07 SK SK447-93A patent/SK280972B6/sk unknown
- 1993-05-07 LV LVP-93-300A patent/LV10447B/en unknown
- 1993-05-07 KR KR1019930007867A patent/KR100278876B1/ko not_active Expired - Fee Related
- 1993-05-07 FI FI932070A patent/FI106525B/fi active
- 1993-05-07 CZ CZ1993840A patent/CZ287192B6/cs not_active IP Right Cessation
-
1994
- 1994-07-06 US US08/271,264 patent/US5472972A/en not_active Expired - Lifetime
- 1994-07-12 EE EE9400019A patent/EE03133B1/xx not_active IP Right Cessation
-
1995
- 1995-05-04 US US08/433,834 patent/US5554391A/en not_active Expired - Lifetime
-
1998
- 1998-03-13 GR GR980400545T patent/GR3026360T3/el unknown
-
2000
- 2000-12-12 CN CNB001307959A patent/CN1149927C/zh not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| Патент США N 4964892, кл. A 01 N 43/80, 1990. Патент Великобритании N 1113618, кл. C 07 D 261/12, 1970. Патент Феликобритании N 1199737, кл. C 07 D 261/12, 1978. Патент Великобритании N 1256835, кл. C 07 D 261/12, 1980. * |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2269264C2 (ru) * | 2000-08-31 | 2006-02-10 | Тор Гмбх | Композиция для борьбы с микроорганизмами, ее применение для борьбы с вредными микроорганизмами |
| WO2005104852A1 (fr) * | 2004-04-29 | 2005-11-10 | Zakrytoe Aktsionernoe Obschestvo 'institut Sistemnyx Innovaciy 'salus' | Preparation fongicide universelle 'donor' |
| EA010839B1 (ru) * | 2004-04-29 | 2008-12-30 | Закрытое Акционерное Общество «Институт Системных Инноваций "Салюс"» | Применение легкорастворимой соли кальция как адаптогена к гидротермическим метеострессам в период вегетации растений и универсальный фунгицидный препарат на ее основе |
| WO2011084085A1 (ru) * | 2010-01-11 | 2011-07-14 | Mokhov Victor Valentinovich | Биоорганический препарат для обработки растений (варианты) |
| US9150461B2 (en) | 2010-01-11 | 2015-10-06 | Astarta, Llc | Bioorganic agent for treating plants (variants) |
| RU2658990C2 (ru) * | 2012-12-31 | 2018-06-26 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Композиции и способы для модулирования скорости образования ebis из дитиокарбаматных фунгицидов |
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