CS214755B2 - Herbicide means and method of making the active component - Google Patents
Herbicide means and method of making the active component Download PDFInfo
- Publication number
- CS214755B2 CS214755B2 CS805419A CS541980A CS214755B2 CS 214755 B2 CS214755 B2 CS 214755B2 CS 805419 A CS805419 A CS 805419A CS 541980 A CS541980 A CS 541980A CS 214755 B2 CS214755 B2 CS 214755B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- formula
- снз
- active ingredient
- halogen
- compound
- Prior art date
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- 239000004009 herbicide Substances 0.000 title description 6
- 238000004519 manufacturing process Methods 0.000 title description 6
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- 239000004480 active ingredient Substances 0.000 claims description 23
- -1 cyano, carboxy Chemical group 0.000 claims description 21
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- 125000000217 alkyl group Chemical group 0.000 claims description 13
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
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- 150000002367 halogens Chemical class 0.000 claims description 8
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- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
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- 238000006396 nitration reaction Methods 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 235000003513 sheep sorrel Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical group OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
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
- A01N37/44—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 nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—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 nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH719779 | 1979-08-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS214755B2 true CS214755B2 (en) | 1982-05-28 |
Family
ID=4321402
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS805419A CS214755B2 (en) | 1979-08-06 | 1980-08-05 | Herbicide means and method of making the active component |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US4490167A (pl) |
| EP (1) | EP0023890B1 (pl) |
| JP (1) | JPS5629560A (pl) |
| BR (1) | BR8004902A (pl) |
| CA (1) | CA1131650A (pl) |
| CS (1) | CS214755B2 (pl) |
| DD (1) | DD152465A5 (pl) |
| DE (1) | DE3066392D1 (pl) |
| ES (1) | ES493995A0 (pl) |
| HU (1) | HU183195B (pl) |
| IL (1) | IL60752A (pl) |
| PL (1) | PL123473B1 (pl) |
| ZA (1) | ZA804742B (pl) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4564385A (en) * | 1979-05-11 | 1986-01-14 | Ppg Industries, Inc. | Herbicidally active substituted diphenyl ether oxime derivatives |
| US4344789A (en) * | 1979-05-11 | 1982-08-17 | Ppg Industries, Inc. | Acids and esters of 5-(2-optionally substituted-4-trifluoromethyl-6-optionally substituted phenoxy)-2-nitro, -halo, or-cyano alpha substituted phenyl carboxy oximes, and method of controlling weeds with them |
| US4551171A (en) * | 1980-02-01 | 1985-11-05 | Rhone-Poulenc, Inc. | 2-Nitro-5-(substituted-phenoxy) phenylalkanone oxime and imine derivatives as herbicides |
| US4633000A (en) * | 1980-02-01 | 1986-12-30 | Rhone Poulenc Agrochimie | 2-nitro-5-(substituted-phenoxy) phenylalkanone oxime and imine derivatives as herbicides |
| FR2549047B1 (fr) * | 1983-07-12 | 1986-03-21 | Rhone Poulenc Agrochimie | Nouveaux herbicides derives d'acides aryloxybenzenes carbonimides |
| CN1005376B (zh) * | 1984-12-12 | 1989-10-11 | 旭化成工业株式会社 | 含有5-(2-氯-4-三氟甲基苯氧基)-2-硝基-α-取代的苯乙酮和/或衍生物肟作为有效成分的除草剂以及消灭不需要的杂草的方法 |
| DE3620166A1 (de) * | 1986-06-14 | 1987-12-17 | Bayer Ag | Verfahren zur herstellung von hydroxybenzaldoxim-o-ethern |
| USRE33989E (en) * | 1986-07-16 | 1992-07-07 | Basf Aktiengesellschaft | Oxime ethers and fungicides containing these compounds |
| DE3623921A1 (de) * | 1986-07-16 | 1988-01-21 | Basf Ag | Oximether und diese enthaltende fungizide |
| DE3901706A1 (de) * | 1988-05-17 | 1989-11-30 | Bayer Ag | Halogensubstituierte phenoxybenzyl(thi)ol-derivate |
| DE69009679T2 (de) * | 1989-11-09 | 1995-02-02 | Ube Industries | Benzylidenaminooxyalkan(thio)carbonsäureamidderivate, Verfahren zu deren Herstellung und Herbizide. |
| DE4014171A1 (de) * | 1990-05-03 | 1991-11-07 | Basf Ag | Cyanochinolinverbindungen |
| US5380913A (en) * | 1990-07-26 | 1995-01-10 | Shionogi & Co., Ltd. | Process for producing methoxyiminoacetamide compounds and intermediates |
| US5650539A (en) * | 1990-07-26 | 1997-07-22 | Shionogi & Co., Ltd. | Process for producing alkoxyiminoacetamide compounds and intermediates |
| JPH0725727B2 (ja) * | 1990-07-26 | 1995-03-22 | 塩野義製薬株式会社 | メトキシイミノアセトアミド化合物の製造法 |
| AU8432291A (en) * | 1990-08-16 | 1992-03-17 | E.I. Du Pont De Nemours And Company | Fungicidal sulfoneoxime esters |
| US6107330A (en) * | 1995-08-07 | 2000-08-22 | Daiichi Pharmaceutical Co., Ltd. | Inhibitor for narcotic analgesic dependence/resistance acquisition |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL111264C (pl) * | 1960-01-01 | |||
| US3394181A (en) * | 1964-06-29 | 1968-07-23 | Sterling Drug Inc | Phenoxy-lower-alkyl-amidoximes and phenylamino-lower-alkyl-amidoximes |
| US3483246A (en) * | 1966-12-05 | 1969-12-09 | Mobil Oil Corp | Aromatic glyoxynitrile oximino carbanates |
| FR2054700A5 (pl) * | 1969-07-23 | 1971-05-07 | Rhone Poulenc Sa | |
| US3799757A (en) * | 1971-11-24 | 1974-03-26 | Monsanto Co | Arylglyoxylonitrileoximes as plant regulants |
| US4152137A (en) * | 1975-09-04 | 1979-05-01 | Ciba-Geigy Corporation | Phenylglyoxylonitrile-2-oxime-cyanomethyl ether as a crop safener |
| CH624552A5 (pl) * | 1975-09-04 | 1981-08-14 | Ciba Geigy Ag | |
| JPS52133905A (en) * | 1976-04-30 | 1977-11-09 | Sumitomo Chem Co Ltd | Preparation of enamides |
| US4123255A (en) * | 1977-01-03 | 1978-10-31 | Chevron Research Company | O-sulfonyl-alpha-cyano 2,6-dihalobenzaldoximes |
| CH632130A5 (en) * | 1977-03-02 | 1982-09-30 | Ciba Geigy Ag | Compositions on the basis of oxime ethers, oxime esters or oxime carbamates which are suitable in agriculture for crop protection |
| BE870068A (fr) * | 1978-08-30 | 1979-02-28 | Ciba Geigy | Procede de lutte selective contre les mauvaises herbes et agent herbicide applique a cet effet |
| US4269775A (en) * | 1978-09-01 | 1981-05-26 | Ciba-Geigy Corporation | Oxime derivatives for protecting plant crops |
| ZA802628B (en) * | 1979-05-11 | 1981-12-30 | Ppg Industries Inc | Acids and esters of 5-(2-optionally substituted-4-trifluoromethyl-6-optionally substituted phenoxy)-2-nitro, -halo, or -cyano alpha substituted phenyl carbonyls, oximes and carboxy oximes |
| US4353736A (en) * | 1980-01-17 | 1982-10-12 | Ciba-Geigy Corporation | Method of selectively controlling weeds and herbicidal diphenyl ether oxime derivatives |
| US4551171A (en) * | 1980-02-01 | 1985-11-05 | Rhone-Poulenc, Inc. | 2-Nitro-5-(substituted-phenoxy) phenylalkanone oxime and imine derivatives as herbicides |
-
1980
- 1980-07-25 US US06/172,312 patent/US4490167A/en not_active Expired - Lifetime
- 1980-07-31 EP EP80810239A patent/EP0023890B1/de not_active Expired
- 1980-07-31 DE DE8080810239T patent/DE3066392D1/de not_active Expired
- 1980-08-01 CA CA357,509A patent/CA1131650A/en not_active Expired
- 1980-08-04 IL IL60752A patent/IL60752A/xx unknown
- 1980-08-04 DD DD80223098A patent/DD152465A5/de unknown
- 1980-08-05 CS CS805419A patent/CS214755B2/cs unknown
- 1980-08-05 HU HU801949A patent/HU183195B/hu unknown
- 1980-08-05 ES ES493995A patent/ES493995A0/es active Granted
- 1980-08-05 BR BR8004902A patent/BR8004902A/pt unknown
- 1980-08-05 ZA ZA00804742A patent/ZA804742B/xx unknown
- 1980-08-06 PL PL1980226098A patent/PL123473B1/pl unknown
- 1980-08-06 JP JP10814780A patent/JPS5629560A/ja active Pending
-
1983
- 1983-01-07 US US06/456,471 patent/US4595410A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE3066392D1 (en) | 1984-03-08 |
| ZA804742B (en) | 1981-08-26 |
| BR8004902A (pt) | 1981-02-17 |
| HU183195B (en) | 1984-04-28 |
| US4595410A (en) | 1986-06-17 |
| IL60752A (en) | 1985-01-31 |
| EP0023890B1 (de) | 1984-02-01 |
| US4490167A (en) | 1984-12-25 |
| PL123473B1 (en) | 1982-10-30 |
| EP0023890A1 (de) | 1981-02-11 |
| JPS5629560A (en) | 1981-03-24 |
| IL60752A0 (en) | 1980-10-26 |
| DD152465A5 (de) | 1981-12-02 |
| ES8106701A1 (es) | 1981-09-01 |
| ES493995A0 (es) | 1981-09-01 |
| PL226098A1 (pl) | 1981-05-22 |
| CA1131650A (en) | 1982-09-14 |
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