CS226030B2 - Herbicide - Google Patents
Herbicide Download PDFInfo
- Publication number
- CS226030B2 CS226030B2 CS815365A CS536581A CS226030B2 CS 226030 B2 CS226030 B2 CS 226030B2 CS 815365 A CS815365 A CS 815365A CS 536581 A CS536581 A CS 536581A CS 226030 B2 CS226030 B2 CS 226030B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- herbicide
- methyl
- herbicidal
- chloro
- composition
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 70
- 239000004009 herbicide Substances 0.000 title claims abstract description 44
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 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 3
- 239000000203 mixture Substances 0.000 claims description 63
- 239000011814 protection agent Substances 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 244000038559 crop plants Species 0.000 claims description 10
- -1 1'-methoxy-6'-methyl-N- (isopropoxymethyl) -2-chloroacetanilide Chemical compound 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical compound ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 claims description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
- UBAGJCNJDBGZPW-UHFFFAOYSA-N 2-chloro-n-methyl-n-[2-methyl-6-(3-methylbutoxy)phenyl]acetamide Chemical compound CC(C)CCOC1=CC=CC(C)=C1N(C)C(=O)CCl UBAGJCNJDBGZPW-UHFFFAOYSA-N 0.000 claims 1
- DVKFMXGJDGDPJC-UHFFFAOYSA-N n-(2-butoxy-6-methylphenyl)-2-chloro-n-methylacetamide Chemical compound CCCCOC1=CC=CC(C)=C1N(C)C(=O)CCl DVKFMXGJDGDPJC-UHFFFAOYSA-N 0.000 claims 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 abstract description 17
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 abstract description 9
- 230000006378 damage Effects 0.000 abstract description 2
- VCIXAWBGWLOGPJ-UHFFFAOYSA-N 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carbothioic s-acid Chemical class FC(F)(F)C=1N=C(Cl)SC=1C(S)=O VCIXAWBGWLOGPJ-UHFFFAOYSA-N 0.000 abstract 1
- 235000015505 Sorghum bicolor subsp. bicolor Nutrition 0.000 abstract 1
- 244000138286 Sorghum saccharatum Species 0.000 abstract 1
- 208000027418 Wounds and injury Diseases 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 208000014674 injury Diseases 0.000 abstract 1
- 239000002689 soil Substances 0.000 description 19
- 241000196324 Embryophyta Species 0.000 description 17
- 240000006394 Sorghum bicolor Species 0.000 description 16
- 239000003755 preservative agent Substances 0.000 description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- 230000002335 preservative effect Effects 0.000 description 14
- 239000010410 layer Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000007787 solid Substances 0.000 description 8
- 230000005764 inhibitory process Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000012258 stirred mixture Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 150000003573 thiols Chemical class 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- UENGBOCGGKLVJJ-UHFFFAOYSA-N 2-chloro-1-(2,4-difluorophenyl)ethanone Chemical compound FC1=CC=C(C(=O)CCl)C(F)=C1 UENGBOCGGKLVJJ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- YYXVCGCMPIVDHN-UHFFFAOYSA-N 1,3-thiazole-5-carbothioic s-acid Chemical compound OC(=S)C1=CN=CS1 YYXVCGCMPIVDHN-UHFFFAOYSA-N 0.000 description 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 description 1
- HRJUIZPPJLMIGB-UHFFFAOYSA-N 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carbonyl chloride Chemical compound FC(F)(F)C=1N=C(Cl)SC=1C(Cl)=O HRJUIZPPJLMIGB-UHFFFAOYSA-N 0.000 description 1
- 235000011331 Brassica Nutrition 0.000 description 1
- 241000219198 Brassica Species 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 244000060234 Gmelina philippensis Species 0.000 description 1
- 235000006679 Mentha X verticillata Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 239000006002 Pepper Substances 0.000 description 1
- 235000016761 Piper aduncum Nutrition 0.000 description 1
- 235000017804 Piper guineense Nutrition 0.000 description 1
- 244000203593 Piper nigrum Species 0.000 description 1
- 235000008184 Piper nigrum Nutrition 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 101100256620 Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) selU gene Proteins 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
- 230000003031 feeding effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- RFPKQOPACVIPNT-UHFFFAOYSA-N o-ethyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carbothioate Chemical compound CCOC(=S)C=1SC(Cl)=NC=1C(F)(F)F RFPKQOPACVIPNT-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000012421 spiking Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 239000002023 wood 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/168,959 US4640702A (en) | 1980-07-14 | 1980-07-14 | 2-chloro-4-trifluoromethyl-thiazolecarbothioic acids useful as herbicidal safeners |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS226030B2 true CS226030B2 (en) | 1984-03-19 |
Family
ID=22613698
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS815365A CS226030B2 (en) | 1980-07-14 | 1981-07-13 | Herbicide |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US4640702A (de) |
| EP (1) | EP0044201B1 (de) |
| JP (1) | JPS5748977A (de) |
| KR (1) | KR850000442B1 (de) |
| AR (1) | AR226906A1 (de) |
| AT (1) | ATE9581T1 (de) |
| AU (1) | AU537626B2 (de) |
| BG (1) | BG36191A3 (de) |
| BR (1) | BR8104453A (de) |
| CA (1) | CA1161441A (de) |
| CS (1) | CS226030B2 (de) |
| DD (2) | DD202233A5 (de) |
| DE (1) | DE3166323D1 (de) |
| DK (1) | DK311281A (de) |
| ES (1) | ES503834A0 (de) |
| HU (1) | HU189520B (de) |
| IL (1) | IL63290A (de) |
| KE (1) | KE3512A (de) |
| MW (1) | MW2781A1 (de) |
| MY (1) | MY8600066A (de) |
| NZ (1) | NZ197698A (de) |
| PH (1) | PH18521A (de) |
| PL (1) | PL127862B1 (de) |
| PT (1) | PT73357B (de) |
| RO (1) | RO82746B (de) |
| ZA (1) | ZA814766B (de) |
| ZM (1) | ZM5581A1 (de) |
| ZW (1) | ZW16081A1 (de) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1174454B (it) * | 1984-01-06 | 1987-07-01 | Montedison Spa | Composti ad attivita'antidotica per la difesa di culture agrarie dall'azione di erbicidi non seletivi |
| US5135927A (en) * | 1987-01-30 | 1992-08-04 | Ciba-Geigy Corporation | Microbicidal composition |
| ATE82275T1 (de) * | 1987-01-30 | 1992-11-15 | Ciba Geigy Ag | Mikrobizide mittel. |
| EP0335831A1 (de) * | 1988-03-15 | 1989-10-04 | Ciba-Geigy Ag | Thiazol-5-carbonsäureamide zum Schützen von Kulturpflanzen vor der phytotoxischen Wirkung von stark wirksamen Herbiziden |
| JP2771280B2 (ja) * | 1989-10-12 | 1998-07-02 | 株式会社扇商會 | 静電塗装装置及び該静電塗装装置用回転部材 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2139570A (en) * | 1935-05-02 | 1938-12-06 | Winthrop Chem Co Inc | Thiazole compounds and manufacture thereof |
| US2726237A (en) * | 1952-08-16 | 1955-12-06 | Eastman Kodak Co | Azo-2-amino-4-trifluoromethylthiazoles |
| US2726247A (en) * | 1953-11-30 | 1955-12-06 | Eastman Kodak Co | 2-amino-4-trifluoromethylthiazole compounds and process for their preparation |
| US3536727A (en) * | 1966-12-22 | 1970-10-27 | Wyeth John & Brother Ltd | Alpha-(2-arylthiazol-4-yl) lower fatty acids and derivatives |
| DE2213865C3 (de) * | 1972-03-22 | 1981-01-22 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Chlorthiazolen |
| US4199506A (en) * | 1978-05-15 | 1980-04-22 | Monsanto Company | 2,4-Disubstituted-5-thiazolecarboxylic acids and derivatives |
| US4336389A (en) * | 1978-05-15 | 1982-06-22 | Monsanto Company | 2-Substituted-4-aryl-5-thiazolecarboxylic acids and their derivatives as safening agents |
| US4317310A (en) * | 1978-11-15 | 1982-03-02 | Monsanto Company | Substituted 2-imino-1,3-dithio and 1,3-oxathio heterocyclic compounds as herbicidal antidotes |
-
1980
- 1980-07-14 US US06/168,959 patent/US4640702A/en not_active Expired - Lifetime
-
1981
- 1981-07-10 DE DE8181303151T patent/DE3166323D1/de not_active Expired
- 1981-07-10 AT AT81303151T patent/ATE9581T1/de not_active IP Right Cessation
- 1981-07-10 ES ES503834A patent/ES503834A0/es active Granted
- 1981-07-10 EP EP81303151A patent/EP0044201B1/de not_active Expired
- 1981-07-13 ZW ZW160/81A patent/ZW16081A1/xx unknown
- 1981-07-13 BR BR8104453A patent/BR8104453A/pt unknown
- 1981-07-13 ZM ZM55/81A patent/ZM5581A1/xx unknown
- 1981-07-13 BG BG052922A patent/BG36191A3/xx unknown
- 1981-07-13 IL IL63290A patent/IL63290A/xx unknown
- 1981-07-13 MW MW27/81A patent/MW2781A1/xx unknown
- 1981-07-13 DD DD81231812A patent/DD202233A5/de unknown
- 1981-07-13 CA CA000381644A patent/CA1161441A/en not_active Expired
- 1981-07-13 PT PT73357A patent/PT73357B/pt unknown
- 1981-07-13 RO RO104866A patent/RO82746B/ro unknown
- 1981-07-13 JP JP56108334A patent/JPS5748977A/ja active Pending
- 1981-07-13 AR AR286062A patent/AR226906A1/es active
- 1981-07-13 NZ NZ197698A patent/NZ197698A/xx unknown
- 1981-07-13 AU AU72794/81A patent/AU537626B2/en not_active Ceased
- 1981-07-13 CS CS815365A patent/CS226030B2/cs unknown
- 1981-07-13 PL PL1981232179A patent/PL127862B1/pl unknown
- 1981-07-13 HU HU812056A patent/HU189520B/hu unknown
- 1981-07-13 PH PH25900A patent/PH18521A/en unknown
- 1981-07-13 KR KR1019810002541A patent/KR850000442B1/ko not_active Expired
- 1981-07-13 DK DK311281A patent/DK311281A/da not_active Application Discontinuation
- 1981-07-13 ZA ZA814766A patent/ZA814766B/xx unknown
-
1982
- 1982-12-10 DD DD82245816A patent/DD208751A5/de unknown
-
1985
- 1985-03-05 KE KE3512A patent/KE3512A/xx unknown
-
1986
- 1986-12-30 MY MY66/86A patent/MY8600066A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AR226906A1 (es) | 1982-08-31 |
| CA1161441A (en) | 1984-01-31 |
| MY8600066A (en) | 1986-12-31 |
| DK311281A (da) | 1982-01-15 |
| PH18521A (en) | 1985-08-02 |
| HU189520B (en) | 1986-07-28 |
| PL232179A1 (de) | 1982-02-01 |
| IL63290A0 (en) | 1981-10-30 |
| RO82746B (ro) | 1984-05-30 |
| ES8203864A1 (es) | 1982-04-16 |
| ZW16081A1 (en) | 1981-10-07 |
| PT73357A (en) | 1981-08-01 |
| DD208751A5 (de) | 1984-04-11 |
| ES503834A0 (es) | 1982-04-16 |
| DD202233A5 (de) | 1983-09-07 |
| ZM5581A1 (en) | 1981-12-21 |
| RO82746A (ro) | 1984-04-12 |
| JPS5748977A (en) | 1982-03-20 |
| MW2781A1 (en) | 1982-09-08 |
| KE3512A (en) | 1985-03-29 |
| PT73357B (en) | 1982-07-30 |
| KR850000442B1 (ko) | 1985-04-05 |
| US4640702A (en) | 1987-02-03 |
| BR8104453A (pt) | 1982-03-30 |
| IL63290A (en) | 1985-05-31 |
| NZ197698A (en) | 1983-06-17 |
| AU7279481A (en) | 1982-01-21 |
| KR830006251A (ko) | 1983-09-20 |
| ZA814766B (en) | 1982-09-29 |
| BG36191A3 (en) | 1984-09-14 |
| DE3166323D1 (en) | 1984-10-31 |
| AU537626B2 (en) | 1984-07-05 |
| ATE9581T1 (de) | 1984-10-15 |
| EP0044201A1 (de) | 1982-01-20 |
| EP0044201B1 (de) | 1984-09-26 |
| PL127862B1 (en) | 1983-12-31 |
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