BG61517B2 - N-фенилсулфонил-n'-триазинилкарбамиди - Google Patents
N-фенилсулфонил-n'-триазинилкарбамиди Download PDFInfo
- Publication number
- BG61517B2 BG61517B2 BG96471A BG9647192A BG61517B2 BG 61517 B2 BG61517 B2 BG 61517B2 BG 96471 A BG96471 A BG 96471A BG 9647192 A BG9647192 A BG 9647192A BG 61517 B2 BG61517 B2 BG 61517B2
- Authority
- BG
- Bulgaria
- Prior art keywords
- hydrogen
- phenylsulfonyl
- alkyl
- formula
- azinylurea
- Prior art date
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- -1 3,3,3-trifluoropropyl Chemical group 0.000 claims abstract description 57
- 150000001875 compounds Chemical class 0.000 claims abstract description 50
- 239000001257 hydrogen Substances 0.000 claims abstract description 32
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 32
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 17
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 15
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000002367 halogens Chemical group 0.000 claims abstract description 9
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 9
- 239000001301 oxygen Substances 0.000 claims abstract description 9
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract description 6
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims abstract description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 3
- 239000011593 sulfur Substances 0.000 claims abstract description 3
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract 2
- 241000196324 Embryophyta Species 0.000 claims description 46
- 239000000203 mixture Substances 0.000 claims description 42
- 239000004480 active ingredient Substances 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 28
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 230000002363 herbicidal effect Effects 0.000 claims description 9
- 230000008635 plant growth Effects 0.000 claims description 9
- 125000000217 alkyl group Chemical group 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
- 235000013339 cereals Nutrition 0.000 claims description 7
- 244000068988 Glycine max Species 0.000 claims description 5
- 235000010469 Glycine max Nutrition 0.000 claims description 5
- 230000001105 regulatory effect Effects 0.000 claims description 5
- 240000008042 Zea mays Species 0.000 claims description 3
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 3
- 230000001276 controlling effect Effects 0.000 claims description 3
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 3
- 235000021374 legumes Nutrition 0.000 claims description 3
- 235000009973 maize Nutrition 0.000 claims description 3
- 229920000742 Cotton Polymers 0.000 claims description 2
- 244000299507 Gossypium hirsutum Species 0.000 claims description 2
- 240000007594 Oryza sativa Species 0.000 claims description 2
- 235000007164 Oryza sativa Nutrition 0.000 claims description 2
- 240000000111 Saccharum officinarum Species 0.000 claims description 2
- 235000007201 Saccharum officinarum Nutrition 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000004995 haloalkylthio group Chemical group 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 235000009566 rice Nutrition 0.000 claims description 2
- FENAOFFCBUFUEY-UHFFFAOYSA-N 1-(benzenesulfonyl)-1-(triazin-4-yl)urea Chemical compound C=1C=CC=CC=1S(=O)(=O)N(C(=O)N)C1=CC=NN=N1 FENAOFFCBUFUEY-UHFFFAOYSA-N 0.000 claims 3
- 230000018109 developmental process Effects 0.000 claims 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 1
- WFRWCLKPIVBOQX-UHFFFAOYSA-N 1-(benzenesulfonyl)-3-(triazin-4-yl)urea Chemical compound C=1C=CC=CC=1S(=O)(=O)NC(=O)NC1=CC=NN=N1 WFRWCLKPIVBOQX-UHFFFAOYSA-N 0.000 claims 1
- QGODEZCNKWFZCL-UHFFFAOYSA-N CC1=NC(=NC(=N1)OC)N(C(=O)N)S(=O)(=O)C2=CC=CC=C2CCC(C)(F)F Chemical compound CC1=NC(=NC(=N1)OC)N(C(=O)N)S(=O)(=O)C2=CC=CC=C2CCC(C)(F)F QGODEZCNKWFZCL-UHFFFAOYSA-N 0.000 claims 1
- LTUNNEGNEKBSEH-UHFFFAOYSA-N Prosulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)CCC(F)(F)F)=N1 LTUNNEGNEKBSEH-UHFFFAOYSA-N 0.000 claims 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 1
- 230000008121 plant development Effects 0.000 claims 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 7
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 5
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 25
- 230000012010 growth Effects 0.000 description 17
- 239000002585 base Substances 0.000 description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
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- 238000006243 chemical reaction Methods 0.000 description 13
- 239000000243 solution Substances 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
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- 238000002360 preparation method Methods 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 235000013877 carbamide Nutrition 0.000 description 8
- 239000000460 chlorine Substances 0.000 description 8
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 7
- 239000004202 carbamide Substances 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 241000209504 Poaceae Species 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000005995 Aluminium silicate Substances 0.000 description 5
- 235000012211 aluminium silicate Nutrition 0.000 description 5
- 239000000969 carrier Substances 0.000 description 5
- 230000035784 germination Effects 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 5
- 239000002736 nonionic surfactant Substances 0.000 description 5
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- 238000001953 recrystallisation Methods 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- PIJUMEVHGDAQBH-UHFFFAOYSA-N 2-(3,3,3-trifluoropropyl)benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1CCC(F)(F)F PIJUMEVHGDAQBH-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
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- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 4
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical class CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 4
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- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- OLQNSNSBYNGMBQ-UHFFFAOYSA-N 1-methyl-3-[2-(3,3,3-trifluoropropyl)phenyl]sulfonylurea Chemical compound CNC(=O)NS(=O)(=O)C1=CC=CC=C1CCC(F)(F)F OLQNSNSBYNGMBQ-UHFFFAOYSA-N 0.000 description 3
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- HONKCVPAORBBSR-UHFFFAOYSA-N n-(oxomethylidene)-2-(3,3,3-trifluoropropyl)benzenesulfonamide Chemical compound FC(F)(F)CCC1=CC=CC=C1S(=O)(=O)N=C=O HONKCVPAORBBSR-UHFFFAOYSA-N 0.000 description 3
- LFXCJFIIYPGASU-UHFFFAOYSA-N phenyl-[2-(3,3,3-trifluoropropyl)phenyl]carbamic acid Chemical compound C=1C=CC=C(CCC(F)(F)F)C=1N(C(=O)O)C1=CC=CC=C1 LFXCJFIIYPGASU-UHFFFAOYSA-N 0.000 description 3
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- 229910021532 Calcite Inorganic materials 0.000 description 2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/78—Halides of sulfonic acids
- C07C309/86—Halides of sulfonic acids having halosulfonyl groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/65—N-sulfonylisocyanates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (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)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH167783 | 1983-03-28 | ||
CH439383 | 1983-08-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
BG61517B2 true BG61517B2 (bg) | 1997-10-31 |
Family
ID=25688357
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BG96471A BG61517B2 (bg) | 1983-03-28 | 1992-06-15 | N-фенилсулфонил-n'-триазинилкарбамиди |
Country Status (15)
Country | Link |
---|---|
US (4) | US4671819A (pt) |
EP (1) | EP0120814B1 (pt) |
JP (2) | JPH0688980B2 (pt) |
AR (1) | AR242027A1 (pt) |
AT (1) | ATE35888T1 (pt) |
AU (2) | AU570037B2 (pt) |
BG (1) | BG61517B2 (pt) |
BR (1) | BR8401404A (pt) |
CA (1) | CA1223589A (pt) |
CY (1) | CY1577A (pt) |
DE (1) | DE3472881D1 (pt) |
DO (1) | DOP1992004859A (pt) |
ES (1) | ES8601920A1 (pt) |
IL (3) | IL71346A (pt) |
PH (1) | PH21379A (pt) |
Families Citing this family (44)
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CA1221689A (en) * | 1982-09-10 | 1987-05-12 | Mark E. Thompson | Herbicidal ortho-alkyl- and ortho-alkenyl-substituted benzenesulfonamides |
AU585761B2 (en) * | 1984-03-07 | 1989-06-22 | E.I. Du Pont De Nemours And Company | Herbicidal fluoroethoxy triazines |
US4849010A (en) * | 1985-04-10 | 1989-07-18 | E. I. Dupont De Nemours And Company | Herbicidal sulfonamides |
ATE38382T1 (de) * | 1984-07-26 | 1988-11-15 | Ciba Geigy Ag | N-arylsulfonyl-n'-triazinyl- und pyrimidinylharnstoffe. |
DE3431917A1 (de) * | 1984-08-30 | 1986-03-13 | Bayer Ag, 5090 Leverkusen | 1-(2-trifluormethoxy-phenylsulfonyl)-3- heteroaryl-(thio)-harnstoffe |
US4802906A (en) * | 1985-02-21 | 1989-02-07 | E. I. Du Pont De Nemours And Company | Herbicidal ortho-sulfonamide benzenesulfonylureas |
AU602654B2 (en) * | 1985-05-10 | 1990-10-25 | E.I. Du Pont De Nemours And Company | Herbicidal o-carbomethoxysulfonylureas |
US4678498A (en) * | 1985-06-12 | 1987-07-07 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
CA1230119A (en) | 1985-11-22 | 1987-12-08 | Craig L. Hillemann | N-2-carboxylphenylsulfonyl-n'-pyrimidin-2-yl or triazin-2-yl-urea compounds |
US4956005A (en) * | 1985-12-23 | 1990-09-11 | E. I. Du Pont De Nemours And Company | Herbicidal orthosulfonamide benzene sulfonylureas |
US4927453A (en) * | 1986-10-17 | 1990-05-22 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
US5108487A (en) * | 1986-10-17 | 1992-04-28 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
FR2628427A2 (fr) * | 1987-06-25 | 1989-09-15 | Rhone Poulenc Agrochimie | Herbicides de type sulfonyluree, leur preparation, les compositions les contenant et leur utilisation |
FR2617167B1 (fr) * | 1987-06-25 | 1989-11-24 | Rhone Poulenc Agrochimie | Herbicides de type sulfonyluree, leur preparation, les compositions les contenant et leur utilisation |
US5215570A (en) * | 1988-10-20 | 1993-06-01 | Ciba-Geigy Corporation | Sulfamoylphenylureas |
DE3842177A1 (de) * | 1988-12-15 | 1990-06-21 | Basf Ag | Substituierte sulfonylharnstoffe |
ATE119163T1 (de) * | 1989-01-11 | 1995-03-15 | Ciba Geigy Ag | Antidots zur verbesserung der kulturpflanzenvertäglichkeit agrochemischer wirkstoffe. |
MY136106A (en) * | 1990-09-06 | 2008-08-29 | Novartis Ag | Synergistic composition comprising a sulfonylurea anda thiadiazolo (3,4-a)pyridazine and method of selective weed control. |
US5220062A (en) * | 1991-05-06 | 1993-06-15 | Ciba-Geigy Corporation | Process for the preparation of benezenesulfonamides |
DE59208724D1 (de) * | 1991-12-12 | 1997-09-04 | Ciba Geigy Ag | Monoklonale Antikörper gegen Sulfonylharnstoffherbiziden und ihre Verwendung zum Nachweis |
AU3496493A (en) | 1992-02-21 | 1993-09-13 | Ciba-Geigy Ag | Sulfonylureas as herbicides |
EP0558448A1 (de) * | 1992-02-26 | 1993-09-01 | Ciba-Geigy Ag | 1,5-Diphenylpyrazol-3-Carbonsäure-Derivate als Antidots für Sulfonylharnstoffherbizide |
DK0639050T3 (da) * | 1992-05-06 | 2001-04-23 | Novartis Ag | Synergistisk middel og fremgangsmåde til selektiv ukrudtsbekæmpelse |
US6017851A (en) * | 1992-05-06 | 2000-01-25 | Novartis Corp. | Synergistic composition and process for selective weed control |
US5508402A (en) * | 1992-08-18 | 1996-04-16 | Ciba-Geigy Corporation | Process for the preparation of N,N'-substituted ureas |
TW232682B (pt) | 1992-08-18 | 1994-10-21 | Ciba Geigy | |
LT3943B (en) | 1993-12-23 | 1996-05-27 | Ciba Geigy Ag | Remedy for cultured plants protection, use of sulphamoyl-phenyl-carbamides for cultured plant protection, herbicidal preparation, process for preparing sulphamoyl-phenyl-carbamides |
JPH09508895A (ja) * | 1994-01-10 | 1997-09-09 | チバーガイギー アクチェンゲゼルシャフト | 除草剤の水和剤配合物 |
BR9606948A (pt) * | 1995-02-13 | 1997-12-23 | Novartis Ag Novartis S A Novar | Composições herbicida e método de controle de plantas daninhas |
JP3548299B2 (ja) * | 1995-08-28 | 2004-07-28 | ジヤトコ株式会社 | 変速機の回転体支持構造 |
US6586367B2 (en) | 1996-09-05 | 2003-07-01 | Syngenta Crop Protection, Inc. | Process for the control of weeds |
DE19836660A1 (de) | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Sojakulturen |
DE19836659A1 (de) | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Baumwollkulturen |
PL214793B1 (pl) | 1998-08-13 | 2013-09-30 | Bayer Cropscience Ag | Zastosowanie kompozycji zawierajacej glifosat i flutiamid do zwalczania szkodliwych roslin w uprawach kukurydzy i sposób zwalczania szkodliwych roslin w uprawach kukurydzy |
EP2052604A1 (de) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Salz des 2-lodo-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl] benzolsulfonamids,Verfahren zu deren Herstellung, sowie deren Verwendung als Herbizide und Pflanzenwachstumregulatoren |
EP2052606A1 (de) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
CN101597246B (zh) * | 2008-06-04 | 2013-07-17 | 江苏省农用激素工程技术研究中心有限公司 | 2-(3,3,3-三氟丙烷基)苯磺酰胺(i)及其中间体制备方法 |
DE102008037620A1 (de) * | 2008-08-14 | 2010-02-18 | Bayer Crop Science Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
RS56603B2 (sr) | 2010-10-15 | 2021-10-29 | Bayer Ip Gmbh | Upotreba als inhibitora herbicida za kontrolu neželjene vegetacije kod beta vulgaris biljaka tolerantnih na als inhibitore herbicida |
UA117447C2 (uk) | 2011-05-04 | 2018-08-10 | Байєр Інтеллектуал Проперті Гмбх | Застосування гербіцидів інгібіторів als для боротьби з небажаною рослинністю на площі вирощування brassica |
LT2931034T (lt) | 2012-12-13 | 2018-10-10 | Bayer Cropscience Ag | Als slopinančių herbicidų panaudojimas nepageidaujamos augmenijos kontrolei augaluose beta vulgaris, kurie tolerantiški als slopinantiems herbicidams |
CN103283759B (zh) * | 2013-06-26 | 2015-10-28 | 联保作物科技有限公司 | 一种玉米田除草组合物及其制剂 |
CN108947873A (zh) * | 2018-08-28 | 2018-12-07 | 江苏省农用激素工程技术研究中心有限公司 | 2-(3,3,3-三氟丙基)苯磺酰胺的制备方法 |
WO2023062184A1 (en) | 2021-10-15 | 2023-04-20 | KWS SAAT SE & Co. KGaA | Als inhibitor herbicide tolerant beta vulgaris mutants |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
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DE1251753B (de) * | 1964-03-21 | 1967-10-12 | Farbwerke Hoechst Aktiengesellschaft vormals Meister Lucius &. Brunmg, Frankfurt/M | Verfahren zur Herstellung von Benzolsulfonylharnstoffen |
OA05625A (fr) * | 1976-04-07 | 1981-04-30 | Du Pont | N-(hétérocyclique aminocarbonyl) aryl sulfonamides herbicides, compositions les contenant et procédés les utilisant . |
US4169719A (en) * | 1976-04-07 | 1979-10-02 | E. I. Du Pont De Nemours And Co. | Herbicidal sulfonamides |
US4348219A (en) * | 1980-07-11 | 1982-09-07 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
ZA814658B (en) * | 1980-07-11 | 1983-02-23 | Du Pont | Herbicidal sulfonamides |
US4332611A (en) * | 1980-07-11 | 1982-06-01 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
US4486589A (en) * | 1980-07-11 | 1984-12-04 | E. I. Du Pont De Nemours And Company | Herbicidal N-(heterocyclicaminocarbonyl)-ortho-haloalkylbenzenesulfonamides |
CH657849A5 (en) * | 1980-07-17 | 1986-09-30 | Ciba Geigy Ag | N-Phenylsulfonyl-N'-pyrimidinyl- and -triazinyl ureas |
US4545811A (en) * | 1981-08-06 | 1985-10-08 | Ciba-Geigy Corporation | N-Phenylsulfonyl-N'-triazinyl-ureas |
CA1221689A (en) * | 1982-09-10 | 1987-05-12 | Mark E. Thompson | Herbicidal ortho-alkyl- and ortho-alkenyl-substituted benzenesulfonamides |
US4515626A (en) * | 1982-10-06 | 1985-05-07 | Ciba Geigy Corporation | N-(Cyclopropyl-triazinyl-n'-(arylsulfonyl) ureas having herbicidal activity |
US4515624A (en) * | 1983-03-23 | 1985-05-07 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
AU571869B2 (en) * | 1983-05-09 | 1988-04-28 | E.I. Du Pont De Nemours And Company | Pyridyl- and pyrimidyl- sulphonamides |
CA1229086A (en) * | 1984-05-09 | 1987-11-10 | Hugh M. Brown | Herbicidal halopyrimidines |
DE3422824A1 (de) * | 1984-06-20 | 1986-01-02 | Celamerck Gmbh & Co Kg, 6507 Ingelheim | Neue herbizid wirksame sulfonylharnstoffe |
JPH0433178A (ja) * | 1990-05-30 | 1992-02-04 | Nec Corp | 画像情報処理方式 |
-
1984
- 1984-03-22 AT AT84810135T patent/ATE35888T1/de not_active IP Right Cessation
- 1984-03-22 DE DE8484810135T patent/DE3472881D1/de not_active Expired
- 1984-03-22 EP EP84810135A patent/EP0120814B1/de not_active Expired
- 1984-03-26 IL IL71346A patent/IL71346A/xx not_active IP Right Cessation
- 1984-03-26 CA CA000450456A patent/CA1223589A/en not_active Expired
- 1984-03-26 AR AR84296110A patent/AR242027A1/es active
- 1984-03-26 IL IL82460A patent/IL82460A/xx not_active IP Right Cessation
- 1984-03-27 AU AU26122/84A patent/AU570037B2/en not_active Expired
- 1984-03-27 JP JP59057495A patent/JPH0688980B2/ja not_active Expired - Lifetime
- 1984-03-27 PH PH30444A patent/PH21379A/en unknown
- 1984-03-27 ES ES530999A patent/ES8601920A1/es not_active Expired
- 1984-03-27 BR BR8401404A patent/BR8401404A/pt not_active IP Right Cessation
-
1985
- 1985-12-17 US US06/810,010 patent/US4671819A/en not_active Expired - Lifetime
-
1987
- 1987-03-27 US US07/030,529 patent/US4759793A/en not_active Expired - Lifetime
- 1987-05-08 IL IL82460A patent/IL82460A0/xx unknown
- 1987-12-29 AU AU83116/87A patent/AU600331B2/en not_active Expired
-
1988
- 1988-04-08 US US07/179,339 patent/US4908467A/en not_active Expired - Lifetime
-
1989
- 1989-11-21 US US07/440,004 patent/US4952726A/en not_active Expired - Lifetime
-
1991
- 1991-12-20 CY CY1577A patent/CY1577A/xx unknown
-
1992
- 1992-01-20 DO DO1992004859A patent/DOP1992004859A/es unknown
- 1992-06-15 BG BG96471A patent/BG61517B2/bg unknown
-
1993
- 1993-05-14 JP JP5135165A patent/JPH0694454B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0694454B2 (ja) | 1994-11-24 |
JPH0688980B2 (ja) | 1994-11-09 |
AU2612284A (en) | 1984-10-04 |
IL71346A0 (en) | 1984-06-29 |
EP0120814B1 (de) | 1988-07-27 |
AU600331B2 (en) | 1990-08-09 |
ATE35888T1 (de) | 1988-08-15 |
US4952726A (en) | 1990-08-28 |
IL82460A (en) | 1988-05-31 |
ES530999A0 (es) | 1985-11-16 |
CY1577A (en) | 1991-12-20 |
IL71346A (en) | 1988-05-31 |
EP0120814A2 (de) | 1984-10-03 |
ES8601920A1 (es) | 1985-11-16 |
DOP1992004859A (es) | 1999-05-05 |
US4671819A (en) | 1987-06-09 |
JPH06145137A (ja) | 1994-05-24 |
US4759793A (en) | 1988-07-26 |
BR8401404A (pt) | 1984-11-06 |
DE3472881D1 (de) | 1988-09-01 |
IL82460A0 (en) | 1987-11-30 |
AU570037B2 (en) | 1988-03-03 |
JPS59181252A (ja) | 1984-10-15 |
AR242027A1 (es) | 1993-02-26 |
CA1223589A (en) | 1987-06-30 |
EP0120814A3 (en) | 1985-08-07 |
AU8311687A (en) | 1988-04-14 |
US4908467A (en) | 1990-03-13 |
PH21379A (en) | 1987-10-15 |
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