DK170906B1 - Forbindelsen 2-[[N-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-N-methylaminocarbonyl]aminosulfonyl]benzoesyremethylester, herbicide præparater og blandinger indeholdende forbindelsen, anvendelse af disse præparater og blandinger samt fremgangsmåde til forbindelsens fremstilling - Google Patents
Forbindelsen 2-[[N-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-N-methylaminocarbonyl]aminosulfonyl]benzoesyremethylester, herbicide præparater og blandinger indeholdende forbindelsen, anvendelse af disse præparater og blandinger samt fremgangsmåde til forbindelsens fremstilling Download PDFInfo
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- DK170906B1 DK170906B1 DK217386A DK217386A DK170906B1 DK 170906 B1 DK170906 B1 DK 170906B1 DK 217386 A DK217386 A DK 217386A DK 217386 A DK217386 A DK 217386A DK 170906 B1 DK170906 B1 DK 170906B1
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- DK
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- Prior art keywords
- compound
- methyl
- methoxy
- triazin
- aminosulfonyl
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- 238000003967 crop rotation Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 150000001987 diarylethers Chemical class 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- OQZCSNDVOWYALR-UHFFFAOYSA-N flurochloridone Chemical compound FC(F)(F)C1=CC=CC(N2C(C(Cl)C(CCl)C2)=O)=C1 OQZCSNDVOWYALR-UHFFFAOYSA-N 0.000 description 1
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
- 229940097068 glyphosate Drugs 0.000 description 1
- 235000011868 grain product Nutrition 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 1
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- RBNIGDFIUWJJEV-UHFFFAOYSA-N methyl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-UHFFFAOYSA-N 0.000 description 1
- BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 description 1
- DSRNRYQBBJQVCW-UHFFFAOYSA-N metoxuron Chemical compound COC1=CC=C(NC(=O)N(C)C)C=C1Cl DSRNRYQBBJQVCW-UHFFFAOYSA-N 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- IKVXBIIHQGXQRQ-UHFFFAOYSA-N propan-2-yl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- BUXTXUBQAKIQKS-UHFFFAOYSA-N sulfuryl diisocyanate Chemical compound O=C=NS(=O)(=O)N=C=O BUXTXUBQAKIQKS-UHFFFAOYSA-N 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- QQOWHRYOXYEMTL-UHFFFAOYSA-N triazin-4-amine Chemical compound N=C1C=CN=NN1 QQOWHRYOXYEMTL-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
- C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Cultivation Of Plants (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Medicines Containing Plant Substances (AREA)
- Plural Heterocyclic Compounds (AREA)
- Cephalosporin Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73278385A | 1985-05-10 | 1985-05-10 | |
US73278385 | 1985-05-10 |
Publications (3)
Publication Number | Publication Date |
---|---|
DK217386D0 DK217386D0 (da) | 1986-05-09 |
DK217386A DK217386A (da) | 1986-11-11 |
DK170906B1 true DK170906B1 (da) | 1996-03-11 |
Family
ID=24944940
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK217386A DK170906B1 (da) | 1985-05-10 | 1986-05-09 | Forbindelsen 2-[[N-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-N-methylaminocarbonyl]aminosulfonyl]benzoesyremethylester, herbicide præparater og blandinger indeholdende forbindelsen, anvendelse af disse præparater og blandinger samt fremgangsmåde til forbindelsens fremstilling |
Country Status (23)
Country | Link |
---|---|
EP (1) | EP0202830B1 (de) |
KR (1) | KR900003851B1 (de) |
CN (1) | CN1016343B (de) |
AT (1) | ATE48273T1 (de) |
AU (1) | AU602654B2 (de) |
CA (1) | CA1230120A (de) |
DE (1) | DE3667171D1 (de) |
DK (1) | DK170906B1 (de) |
ES (1) | ES8800672A1 (de) |
FI (1) | FI90188C (de) |
GR (1) | GR861214B (de) |
HU (1) | HU200079B (de) |
IE (1) | IE58713B1 (de) |
IL (1) | IL78749A (de) |
LT (1) | LT3307B (de) |
NO (1) | NO170683C (de) |
NZ (1) | NZ216104A (de) |
PT (1) | PT82556B (de) |
RU (2) | RU1837771C (de) |
SU (1) | SU1701103A3 (de) |
TR (1) | TR23039A (de) |
UA (1) | UA4200A (de) |
ZA (1) | ZA863461B (de) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3716657A1 (de) * | 1987-05-19 | 1988-12-01 | Basf Ag | Herbizide sulfonamide, verfahren zu ihrer herstellung und ihre verwendung zur beeinflussung des pflanzenwachstums |
AP112A (en) * | 1988-03-16 | 1990-03-05 | Ici South Africa Ltd | Herbicides. |
HU208610B (en) | 1988-06-28 | 1993-12-28 | Du Pont | Pesticidal and plant growth regulating composition in tablet form |
IL88135A (en) * | 1988-10-24 | 1994-04-12 | Bromine Compounds Ltd | Process for the preparation of 3-phenoxybenzylalcohol |
CN1066016C (zh) * | 1996-01-18 | 2001-05-23 | 化学工业部沈阳化工研究院 | 一种除草混剂 |
CN1068039C (zh) * | 1997-02-25 | 2001-07-04 | 石油大学(北京) | 烃基润滑脂及其制备方法 |
EP2052606A1 (de) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
DE102008037620A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Crop Science Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
US9668483B1 (en) | 2015-12-01 | 2017-06-06 | Rotam Agrochem Inernational Company Limited | Synergistic herbicidal composition and use thereof |
US9643936B1 (en) | 2015-12-01 | 2017-05-09 | Rotam Agrochem International Company Limited | Form of tribenuron-methyl, a process for its preparation and use of the same |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4383113A (en) * | 1978-05-30 | 1983-05-10 | E. I. Du Pont De Nemours And Company | Agricultural sulfonamides |
EP0101670B1 (de) * | 1982-08-23 | 1988-03-09 | Ciba-Geigy Ag | Verfahren zur Herstellung von herbiziden und pflanzenwuchsregulierenden Sulfonylharnstoffen |
US4780125A (en) * | 1982-09-01 | 1988-10-25 | Ciba-Geigy Corporation | N-phenylsulfonyl-N'-triazinylureas |
ATE35888T1 (de) * | 1983-03-28 | 1988-08-15 | Ciba Geigy Ag | N-phenylsulfonyl-n'-pyrimidinyl- und triazinylharnstoffe. |
EP0124295B1 (de) * | 1983-04-04 | 1991-04-03 | E.I. Du Pont De Nemours And Company | Stabilisierte wässerige Formulierungen von Sulfonylharnstoffen |
-
1986
- 1986-05-06 CA CA000508533A patent/CA1230120A/en not_active Expired
- 1986-05-06 AU AU57188/86A patent/AU602654B2/en not_active Expired
- 1986-05-08 SU SU4027602A patent/SU1701103A3/ru active
- 1986-05-08 UA UA4027602A patent/UA4200A/uk unknown
- 1986-05-09 HU HU861932A patent/HU200079B/hu unknown
- 1986-05-09 ZA ZA863461A patent/ZA863461B/xx unknown
- 1986-05-09 TR TR244/86A patent/TR23039A/xx unknown
- 1986-05-09 FI FI861959A patent/FI90188C/fi not_active IP Right Cessation
- 1986-05-09 EP EP86303538A patent/EP0202830B1/de not_active Expired
- 1986-05-09 DE DE8686303538T patent/DE3667171D1/de not_active Expired - Lifetime
- 1986-05-09 IE IE123486A patent/IE58713B1/en not_active IP Right Cessation
- 1986-05-09 AT AT86303538T patent/ATE48273T1/de not_active IP Right Cessation
- 1986-05-09 DK DK217386A patent/DK170906B1/da not_active IP Right Cessation
- 1986-05-09 NO NO861855A patent/NO170683C/no not_active IP Right Cessation
- 1986-05-09 IL IL78749A patent/IL78749A/xx not_active IP Right Cessation
- 1986-05-09 NZ NZ216104A patent/NZ216104A/xx unknown
- 1986-05-09 ES ES554849A patent/ES8800672A1/es not_active Expired
- 1986-05-09 KR KR1019860003620A patent/KR900003851B1/ko not_active Expired
- 1986-05-09 PT PT82556A patent/PT82556B/pt unknown
- 1986-05-09 GR GR861214A patent/GR861214B/el unknown
- 1986-05-10 CN CN86103235A patent/CN1016343B/zh not_active Expired
-
1989
- 1989-12-12 RU SU894742594A patent/RU1837771C/ru active
-
1992
- 1992-04-20 RU SU925011399A patent/RU2093512C1/ru active
-
1993
- 1993-03-18 LT LTIP430A patent/LT3307B/lt not_active IP Right Cessation
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
B1 | Patent granted (law 1993) | ||
PUP | Patent expired |