DD202233A5 - Verfahren und zusammensetzung zur verminderung der herbiziden schaedigung von kulturpflanzen - Google Patents
Verfahren und zusammensetzung zur verminderung der herbiziden schaedigung von kulturpflanzen Download PDFInfo
- Publication number
- DD202233A5 DD202233A5 DD81231812A DD23181281A DD202233A5 DD 202233 A5 DD202233 A5 DD 202233A5 DD 81231812 A DD81231812 A DD 81231812A DD 23181281 A DD23181281 A DD 23181281A DD 202233 A5 DD202233 A5 DD 202233A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- item
- methyl
- herbicide
- chloroacetanilide
- haloacetanilide
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title claims abstract description 45
- 239000000203 mixture Substances 0.000 title claims description 26
- 238000000034 method Methods 0.000 title claims description 22
- 240000006394 Sorghum bicolor Species 0.000 claims abstract description 16
- 230000001681 protective effect Effects 0.000 claims abstract description 9
- 230000002363 herbicidal effect Effects 0.000 claims description 49
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical group CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 claims description 23
- 241000196324 Embryophyta Species 0.000 claims description 22
- 239000003223 protective agent Substances 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 19
- 239000002689 soil Substances 0.000 claims description 18
- 230000006378 damage Effects 0.000 claims description 14
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- -1 2'-isopentoxy-6'-ethyl-N-ethyl-2-chloroacetanilide Chemical compound 0.000 claims description 3
- 240000008042 Zea mays Species 0.000 claims description 3
- 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 2
- 231100001184 nonphytotoxic Toxicity 0.000 claims 2
- YGTYRMDZBFYUCE-UHFFFAOYSA-N 2-chloro-n-(2-methoxy-6-methylphenyl)-n-(propan-2-yloxymethyl)acetamide Chemical compound COC1=CC=CC(C)=C1N(COC(C)C)C(=O)CCl YGTYRMDZBFYUCE-UHFFFAOYSA-N 0.000 claims 1
- 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
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 abstract description 14
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- 244000038559 crop plants Species 0.000 abstract description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 21
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 11
- 239000003755 preservative agent Substances 0.000 description 11
- 230000002335 preservative effect Effects 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 230000005764 inhibitory process Effects 0.000 description 8
- 239000007787 solid Substances 0.000 description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 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
- 244000062793 Sorghum vulgare Species 0.000 description 3
- 235000019713 millet Nutrition 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 239000012258 stirred mixture Substances 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- 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 2
- SCCLKMYKNMNNNV-UHFFFAOYSA-N 2-chloro-4-(trifluoromethyl)-3H-1,3-thiazole-2-carbothioic S-acid Chemical compound FC(F)(F)C1=CSC(Cl)(C(S)=O)N1 SCCLKMYKNMNNNV-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000011814 protection agent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 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
- VVAWDAVSESAHRD-UHFFFAOYSA-N 2-chloro-4-(trifluoromethyl)-1,3-thiazol-1-ium-1-carbonyl chloride Chemical compound O=C([S+]1C(Cl)=NC(C(F)(F)F)=C1)Cl VVAWDAVSESAHRD-UHFFFAOYSA-N 0.000 description 1
- NKCXALLPUHSJIO-UHFFFAOYSA-N 2-chloro-n-(2-methoxy-6-methylphenyl)-n-propan-2-yloxypropanamide Chemical compound COC1=CC=CC(C)=C1N(OC(C)C)C(=O)C(C)Cl NKCXALLPUHSJIO-UHFFFAOYSA-N 0.000 description 1
- QHLXBFOLLOJTTD-UHFFFAOYSA-N 2-chloro-n-methyl-2-(3-methylbutoxy)-n-(2-methylphenyl)acetamide Chemical compound CC(C)CCOC(Cl)C(=O)N(C)C1=CC=CC=C1C QHLXBFOLLOJTTD-UHFFFAOYSA-N 0.000 description 1
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical compound ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 description 1
- 240000002245 Acer pensylvanicum Species 0.000 description 1
- 235000006760 Acer pensylvanicum Nutrition 0.000 description 1
- 240000001592 Amaranthus caudatus Species 0.000 description 1
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 1
- HNVPDJIAKTXWBA-UHFFFAOYSA-N C(C1=C(N=C(S1)Cl)C(F)(F)F)C(=O)S Chemical compound C(C1=C(N=C(S1)Cl)C(F)(F)F)C(=O)S HNVPDJIAKTXWBA-UHFFFAOYSA-N 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 240000000275 Persicaria hydropiper Species 0.000 description 1
- 235000017337 Persicaria hydropiper Nutrition 0.000 description 1
- 244000007853 Sarothamnus scoparius Species 0.000 description 1
- 240000003461 Setaria viridis Species 0.000 description 1
- 235000002248 Setaria viridis Nutrition 0.000 description 1
- 235000010086 Setaria viridis var. viridis Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 229960001413 acetanilide Drugs 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N alpha-methyl toluene Natural products CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- UENWRTRMUIOCKN-UHFFFAOYSA-N benzyl thiol Chemical compound SCC1=CC=CC=C1 UENWRTRMUIOCKN-UHFFFAOYSA-N 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 235000008216 herbs Nutrition 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000000314 lubricant Substances 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
- 239000002609 medium Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000002829 reductive effect Effects 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
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000010626 work up procedure Methods 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)
- General Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (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 |
|---|---|
| DD202233A5 true DD202233A5 (de) | 1983-09-07 |
Family
ID=22613698
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD81231812A DD202233A5 (de) | 1980-07-14 | 1981-07-13 | Verfahren und zusammensetzung zur verminderung der herbiziden schaedigung von kulturpflanzen |
| DD82245816A DD208751A5 (de) | 1980-07-14 | 1982-12-10 | Samen von vor schaedigung durch ein 2-halogen-acetanilid-herbizid geschuetzten kulturpflanzen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD82245816A DD208751A5 (de) | 1980-07-14 | 1982-12-10 | Samen von vor schaedigung durch ein 2-halogen-acetanilid-herbizid geschuetzten kulturpflanzen |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US4640702A (cs) |
| EP (1) | EP0044201B1 (cs) |
| JP (1) | JPS5748977A (cs) |
| KR (1) | KR850000442B1 (cs) |
| AR (1) | AR226906A1 (cs) |
| AT (1) | ATE9581T1 (cs) |
| AU (1) | AU537626B2 (cs) |
| BG (1) | BG36191A3 (cs) |
| BR (1) | BR8104453A (cs) |
| CA (1) | CA1161441A (cs) |
| CS (1) | CS226030B2 (cs) |
| DD (2) | DD202233A5 (cs) |
| DE (1) | DE3166323D1 (cs) |
| DK (1) | DK311281A (cs) |
| ES (1) | ES503834A0 (cs) |
| HU (1) | HU189520B (cs) |
| IL (1) | IL63290A (cs) |
| KE (1) | KE3512A (cs) |
| MW (1) | MW2781A1 (cs) |
| MY (1) | MY8600066A (cs) |
| NZ (1) | NZ197698A (cs) |
| PH (1) | PH18521A (cs) |
| PL (1) | PL127862B1 (cs) |
| PT (1) | PT73357B (cs) |
| RO (1) | RO82746B (cs) |
| ZA (1) | ZA814766B (cs) |
| ZM (1) | ZM5581A1 (cs) |
| ZW (1) | ZW16081A1 (cs) |
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 |
| ATE82275T1 (de) * | 1987-01-30 | 1992-11-15 | Ciba Geigy Ag | Mikrobizide mittel. |
| US5135927A (en) * | 1987-01-30 | 1992-08-04 | Ciba-Geigy Corporation | Microbicidal composition |
| 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/en not_active Expired
- 1981-07-13 ZW ZW160/81A patent/ZW16081A1/xx unknown
- 1981-07-13 PL PL1981232179A patent/PL127862B1/pl unknown
- 1981-07-13 DD DD81231812A patent/DD202233A5/de unknown
- 1981-07-13 KR KR1019810002541A patent/KR850000442B1/ko not_active Expired
- 1981-07-13 CS CS815365A patent/CS226030B2/cs unknown
- 1981-07-13 ZM ZM55/81A patent/ZM5581A1/xx unknown
- 1981-07-13 AU AU72794/81A patent/AU537626B2/en not_active Ceased
- 1981-07-13 JP JP56108334A patent/JPS5748977A/ja active Pending
- 1981-07-13 NZ NZ197698A patent/NZ197698A/xx unknown
- 1981-07-13 PT PT73357A patent/PT73357B/pt unknown
- 1981-07-13 ZA ZA814766A patent/ZA814766B/xx unknown
- 1981-07-13 DK DK311281A patent/DK311281A/da not_active Application Discontinuation
- 1981-07-13 BG BG052922A patent/BG36191A3/xx unknown
- 1981-07-13 PH PH25900A patent/PH18521A/en unknown
- 1981-07-13 AR AR286062A patent/AR226906A1/es active
- 1981-07-13 CA CA000381644A patent/CA1161441A/en not_active Expired
- 1981-07-13 MW MW27/81A patent/MW2781A1/xx unknown
- 1981-07-13 IL IL63290A patent/IL63290A/xx unknown
- 1981-07-13 HU HU812056A patent/HU189520B/hu unknown
- 1981-07-13 RO RO104866A patent/RO82746B/ro unknown
- 1981-07-13 BR BR8104453A patent/BR8104453A/pt 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 |
|---|---|
| JPS5748977A (en) | 1982-03-20 |
| MW2781A1 (en) | 1982-09-08 |
| BR8104453A (pt) | 1982-03-30 |
| ATE9581T1 (de) | 1984-10-15 |
| ES8203864A1 (es) | 1982-04-16 |
| CA1161441A (en) | 1984-01-31 |
| ZA814766B (en) | 1982-09-29 |
| PH18521A (en) | 1985-08-02 |
| AU7279481A (en) | 1982-01-21 |
| AR226906A1 (es) | 1982-08-31 |
| RO82746B (ro) | 1984-05-30 |
| KR830006251A (ko) | 1983-09-20 |
| AU537626B2 (en) | 1984-07-05 |
| MY8600066A (en) | 1986-12-31 |
| HU189520B (en) | 1986-07-28 |
| KR850000442B1 (ko) | 1985-04-05 |
| EP0044201A1 (en) | 1982-01-20 |
| PL127862B1 (en) | 1983-12-31 |
| US4640702A (en) | 1987-02-03 |
| PT73357A (en) | 1981-08-01 |
| KE3512A (en) | 1985-03-29 |
| ZW16081A1 (en) | 1981-10-07 |
| PT73357B (en) | 1982-07-30 |
| IL63290A (en) | 1985-05-31 |
| PL232179A1 (cs) | 1982-02-01 |
| ZM5581A1 (en) | 1981-12-21 |
| BG36191A3 (en) | 1984-09-14 |
| ES503834A0 (es) | 1982-04-16 |
| RO82746A (ro) | 1984-04-12 |
| DK311281A (da) | 1982-01-15 |
| EP0044201B1 (en) | 1984-09-26 |
| IL63290A0 (en) | 1981-10-30 |
| CS226030B2 (en) | 1984-03-19 |
| DE3166323D1 (en) | 1984-10-31 |
| DD208751A5 (de) | 1984-04-11 |
| NZ197698A (en) | 1983-06-17 |
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