RU99122016A - SOLID MIXTURES BASED ON SULPHONILKARBAMIDES AND AUXILIARY FACILITIES - Google Patents
SOLID MIXTURES BASED ON SULPHONILKARBAMIDES AND AUXILIARY FACILITIESInfo
- Publication number
- RU99122016A RU99122016A RU99122016/04A RU99122016A RU99122016A RU 99122016 A RU99122016 A RU 99122016A RU 99122016/04 A RU99122016/04 A RU 99122016/04A RU 99122016 A RU99122016 A RU 99122016A RU 99122016 A RU99122016 A RU 99122016A
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- halogen
- hydrogen
- alkoxy
- group
- Prior art date
Links
- 239000008247 solid mixture Substances 0.000 title claims 7
- -1 sulfonyl carbamides Chemical class 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 150000002367 halogens Chemical class 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 235000013877 carbamide Nutrition 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 229920001577 copolymer Polymers 0.000 claims 2
- 229920000728 polyester Polymers 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- QPJDMGCKMHUXFD-UHFFFAOYSA-N Cyanogen chloride Chemical compound ClC#N QPJDMGCKMHUXFD-UHFFFAOYSA-N 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 150000005215 alkyl ethers Chemical class 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- 229960000539 carbamide Drugs 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 230000002363 herbicidal Effects 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- XNOUKSCKJOEFNJ-UHFFFAOYSA-N prop-2-ene-1-sulfinate Chemical group [O-]S(=O)C[C+]=C XNOUKSCKJOEFNJ-UHFFFAOYSA-N 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims 1
Claims (7)
где R1 означает С1-С4-алкил, который может нести от одной до пяти следующих групп: метокси, этокси, SO2CH3, циано, хлор, фтор, SCH3, S(O)СН3; галоген; группу ER19, в которой Е означает О, S или NR20; COOR12; NO2; S(O)nR17, SO2NR15R16, CONR13R14;
R2 означает водород, метил, галоген, метокси, нитро, циано, трифторметил, трифторметокси, дифторметокси или метилтио;
Y F, CF3, CF2Cl, CF2H, OCF3, OCF2Cl, С1-С4-алкил или С1-С4-алкокси;
Х С1-С2-алкокси, С1-С2-алкил, С1-С2-алкилтио, С1-С2-алкиламино, ди-С1-С2-алкиламино, галоген, С1-С2-галогеналкил, С1-С2-галогеналкокси;
R означает водород или метил;
R19 С1-С4-алкил, С2-С4-алкенил, С2-С4-алкинил или С3-С6-циклоалкил, которые могут нести 1 до 5 атомов галогена. Если Е означает О или NR20, R19 означает еще метилсульфонил, этилсульфонил, трифторметилсульфонил, аллилсульфонил, пропаргилсульфонил или диметилсульфамоил;
R20 означает водород, метил или этил;
R12 означает С1-С4-алкильную группу, которая может нести до трех следующих радикалов: галоген, С1-С4-алкокси, аллил или пропаргил;
R17 означает С1-С4-алкильную группу, которая может нести до трех следующих радикалов: галоген, С1-С4-алкокси, аллил или пропаргил;
R15 означает водород, С1-С2-алкоксигруппу или С1-С4-алкильную группу;
R16 означает водород или С1-С4-алкильную группу;
n имеет значение 1 или 2
Z означает N, СН.2. The solid mixture according to claim 1, containing sulfonylcarbamide formula I
where R 1 means 1 -C 4 -alkyl, which can carry from one to five of the following groups: methoxy, ethoxy, SO 2 CH 3 , cyano, chlorine, fluorine, SCH 3 , S (O) CH 3 ; halogen; group ER 19 , in which E represents O, S or NR 20 ; COOR 12 ; NO 2 ; S (O) n R 17 , SO 2 NR 15 R 16 , CONR 13 R 14 ;
R 2 is hydrogen, methyl, halogen, methoxy, nitro, cyano, trifluoromethyl, trifluoromethoxy, difluoromethoxy, or methylthio;
YF, CF 3 , CF 2 Cl, CF 2 H, OCF 3 , OCF 2 Cl, C 1 -C 4 alkyl or C 1 -C 4 alkoxy;
X C 1 -C 2 -alkoxy, C 1 -C 2 -alkyl, C 1 -C 2 -alkylthio, C 1 -C 2 -alkylamino, di-C 1 -C 2 -alkylamino, halogen, C 1 -C 2 haloalkyl, C 1 -C 2 haloalkoxy;
R is hydrogen or methyl;
R 19 C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl or C 3 -C 6 -cycloalkyl, which can carry 1 to 5 halogen atoms. If E is O or NR 20 , R 19 is also methylsulfonyl, ethylsulfonyl, trifluoromethylsulfonyl, allylsulfonyl, propargylsulfonyl, or dimethylsulfamoyl;
R 20 is hydrogen, methyl or ethyl;
R 12 means C 1 -C 4 is an alkyl group, which can carry up to three of the following radicals: halogen, C 1 -C 4 -alkoxy, allyl or propargyl;
R 17 means C 1 -C 4 is an alkyl group, which can carry up to three of the following radicals: halogen, C 1 -C 4 -alkoxy, allyl or propargyl;
R 15 is hydrogen, a C 1 -C 2 alkoxy group or a C 1 -C 4 alkyl group;
R 16 is hydrogen or a C 1 -C 4 alkyl group;
n is 1 or 2
Z means N, CH.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19712225 | 1997-03-24 | ||
DE19712225 | 1997-03-24 | ||
DE19712225.6 | 1997-03-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU99122016A true RU99122016A (en) | 2001-07-20 |
RU2187933C2 RU2187933C2 (en) | 2002-08-27 |
Family
ID=7824394
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU99122016/04A RU2187933C2 (en) | 1997-03-24 | 1998-03-12 | Solid herbicide mixture, method of control of weed growth, method of herbicide preparation preparing |
Country Status (18)
Country | Link |
---|---|
US (1) | US6242382B1 (en) |
EP (1) | EP0971590B1 (en) |
AR (1) | AR012155A1 (en) |
AT (1) | ATE241273T1 (en) |
AU (1) | AU7520698A (en) |
BR (1) | BR9808037B1 (en) |
CA (1) | CA2284198C (en) |
CO (1) | CO5040003A1 (en) |
DE (1) | DE59808543D1 (en) |
DK (1) | DK0971590T3 (en) |
ES (1) | ES2201491T3 (en) |
HU (1) | HU228225B1 (en) |
PL (1) | PL190381B1 (en) |
RU (1) | RU2187933C2 (en) |
TW (1) | TW453856B (en) |
UA (1) | UA56226C2 (en) |
WO (1) | WO1998042192A1 (en) |
ZA (1) | ZA982439B (en) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW529910B (en) * | 1997-01-30 | 2003-05-01 | Basf Ag | Solid mixtures based on sulfonylureas and adjuvants |
DE10029169A1 (en) | 2000-06-19 | 2002-01-03 | Aventis Cropscience Gmbh | Herbicidal agents |
DE10036002A1 (en) | 2000-07-25 | 2002-02-14 | Aventis Cropscience Gmbh | Herbicidal agents |
TWI243019B (en) * | 2000-08-31 | 2005-11-11 | Basf Ag | Process for the preparation of a solid herbicidal formulation |
DE10231615A1 (en) * | 2002-07-12 | 2004-02-05 | Bayer Cropscience Gmbh | Fixed adjuvants |
DE10307078A1 (en) * | 2003-02-19 | 2004-09-09 | Bayer Cropscience Gmbh | Process for the production of water-dispersible granules |
US8715734B2 (en) * | 2004-02-24 | 2014-05-06 | Sandoz Ag | Amoxicilline instant granulate |
DE102005009321A1 (en) * | 2005-03-01 | 2006-09-07 | Degussa Ag | Suspension, useful for coloring antistatic equipments, comprises water insoluble coloring agents, a heterocyclic compound and water and/or polyvalent alcohol |
DE102005037336A1 (en) * | 2005-08-04 | 2007-02-08 | Degussa Ag | Carbon material |
EP1928232B1 (en) * | 2005-09-16 | 2016-07-13 | Bayer Intellectual Property GmbH | Solid formulation |
DE102006037079A1 (en) * | 2006-08-07 | 2008-02-14 | Evonik Degussa Gmbh | Carbon black, process for producing carbon black and apparatus for carrying out the process |
EP1902618A1 (en) * | 2006-08-17 | 2008-03-26 | Bayer CropScience AG | Process for the preparation of salts of sulfonamides |
DE102007060307A1 (en) * | 2007-12-12 | 2009-06-18 | Evonik Degussa Gmbh | Process for the aftertreatment of carbon black |
DE102008026894A1 (en) * | 2008-06-05 | 2009-12-10 | Evonik Degussa Gmbh | Ink jet ink |
DE102008044116A1 (en) * | 2008-11-27 | 2010-06-02 | Evonik Degussa Gmbh | Pigment granules, process for their preparation and use |
ATE516330T1 (en) * | 2008-12-12 | 2011-07-15 | Evonik Carbon Black Gmbh | INK JET INK |
WO2011012495A1 (en) * | 2009-07-30 | 2011-02-03 | Basf Se | Granules containing prohexadione calcium and sulfate |
AR081621A1 (en) * | 2010-02-04 | 2012-10-10 | Bayer Cropscience Ag | PROCEDURE FOR THE PRODUCTION OF STABLE FORMULATIONS OF SOLID SULFONAMID MATERIALS |
DE102010002244A1 (en) | 2010-02-23 | 2011-08-25 | Evonik Carbon Black GmbH, 63457 | Carbon black, process for its preparation and its use |
EA019754B1 (en) * | 2011-07-13 | 2014-06-30 | Юрий Аглямович ГАРИПОВ | Synergetic herbicidal composition |
JP6203813B2 (en) | 2012-04-02 | 2017-09-27 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | Granules that can be obtained by pulverizing agricultural chemicals and silica, adding an adjuvant, and fluidized bed granulation |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3643246A1 (en) * | 1986-12-18 | 1988-06-30 | Basf Ag | AGENT FOR ABSCISSION OF PLANT PARTS |
US4933000A (en) * | 1987-10-05 | 1990-06-12 | Ciba-Geigy Corporation | Herbicidal compound concentrate |
JP2569342B2 (en) | 1987-10-22 | 1997-01-08 | 石原産業株式会社 | Herbicidal suspension composition |
US5236887B1 (en) * | 1991-05-03 | 1996-04-16 | Dowelanco | Herbicidal heterocyclic sulfonylurea compositions safened by herbicidal acids such as 2,4-d below a ph of 5 |
CA2087930C (en) | 1992-01-28 | 1997-07-22 | Tsunezo Yoshida | Chemically stabilized herbicidal oil-based suspension |
US5679128A (en) * | 1995-01-31 | 1997-10-21 | Latting; John Alvis | Dry-bonded nonionic adjuvants |
-
1998
- 1998-03-12 ES ES98922619T patent/ES2201491T3/en not_active Expired - Lifetime
- 1998-03-12 EP EP98922619A patent/EP0971590B1/en not_active Expired - Lifetime
- 1998-03-12 WO PCT/EP1998/001441 patent/WO1998042192A1/en active IP Right Grant
- 1998-03-12 CA CA002284198A patent/CA2284198C/en not_active Expired - Fee Related
- 1998-03-12 DK DK98922619T patent/DK0971590T3/en active
- 1998-03-12 RU RU99122016/04A patent/RU2187933C2/en not_active IP Right Cessation
- 1998-03-12 DE DE59808543T patent/DE59808543D1/en not_active Expired - Lifetime
- 1998-03-12 PL PL98335963A patent/PL190381B1/en not_active IP Right Cessation
- 1998-03-12 BR BRPI9808037-7A patent/BR9808037B1/en not_active IP Right Cessation
- 1998-03-12 AU AU75206/98A patent/AU7520698A/en not_active Abandoned
- 1998-03-12 AT AT98922619T patent/ATE241273T1/en not_active IP Right Cessation
- 1998-03-12 HU HU0001516A patent/HU228225B1/en not_active IP Right Cessation
- 1998-03-12 US US09/381,548 patent/US6242382B1/en not_active Expired - Lifetime
- 1998-03-24 TW TW087104422A patent/TW453856B/en not_active IP Right Cessation
- 1998-03-24 CO CO98016380A patent/CO5040003A1/en unknown
- 1998-03-24 AR ARP980101338A patent/AR012155A1/en active IP Right Grant
- 1998-03-28 ZA ZA9802439A patent/ZA982439B/en unknown
- 1998-12-03 UA UA99105795A patent/UA56226C2/en unknown
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