120923-37-7Relevant articles and documents
HERBICIDAL COMPOSITIONS
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, (2022/03/02)
The present invention provides compositions comprising herbicidally active compounds (A) and (B), where (A) represents one or more compounds of the general formula (I) or agrochemically compatible salts thereof [component (A)], and (B) represents one or more herbicides [component (B)]. The application further relates to a method and to the use of the herbicidal composition according to the invention for controlling harmful plants or for regulating growth.
Herbicidal mixtures having a synergistic effect
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, (2008/06/13)
PCT No. PCT/EP96/03996 Sec. 371 Date Feb. 17, 1998 Sec. 102(e) Date Feb. 17, 1998 PCT Filed Sep. 12, 1996 PCT Pub. No. WO97/10714 PCT Pub. Date Mar. 27, 1997A composition comprising at least one sulfonylurea of the formula I wherein R1 is substituted alkyl; halogen; a group ER6 (E=O, S or NR7); COOR8; NO2; S(O)oR9; SO2NR10R11; or CONR10R11; R2 is hydrogen, alkyl, alkenyl, alkynyl, halogen, alkoxy, haloalkoxy, haloalkyl, alkylsulfonyl, nitro, cyano or alkylthio; R3 is F, CF3, CF2Cl, CF2H, OCF3, OCF2Cl, or, if R1 is CO2CH3 and R2 is simultaneously fluorine, R3 is Cl, or, if R1 is CH2CF3 or CF2CF3, R3 is methyl, or, if R4 is OCF3 or OCF2Cl, R3 is OCF2H or OCF2Br; R4 is alkoxy, alkyl, alkylthio, alkylamino, dialkylamino, halogen, haloalkyl or haloalkoxy; and R5 is hydrogen, alkoxy or alkyl; or an enviromentally compatible salt of I, and an aryloxyalkanoic acid selected from the group consisting of 2,4-D, 2,4-DB, clomeprop, dichlorprop, dichlorprop-P, dichlorprop-P (2,4-DP-P), fenoprop (2,4,5-TP), fluoroxypyr, MCPA, MCPB, mecoprop, mecoprop-P, napropamide, napropanilide, triclopyr, and an enviromentally compatible salt thereof exhibits a synergistic herbicidal effect.
Processes for preparing sulfonylureas
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, (2008/06/13)
Compounds of the formula I or salts thereof, STR1 in which X is oxygen, --O--NR2 -- or --SO2 --NR2 --, and Y is N or CH, R1 is (C1 -C6)alkyl, (C2 -C6)alkenyl or (C2 -C6)alkynyl, which are in each case optionally substituted, or, in the case where X=oxygen, also (subst.) phenyl, R2 is H, (C1 -C6)alkyl, (C2 -C6)alkenyl or -alkynyl or (C3 -C6) cycloalkyl, R3 and R4 are H, (subst.) (C1 -C4)alkyl or (subst.) (C1 -C4)alkoxy or halogen, (C1 -C4)alkylthio, (C1 -C4)alkylamino or di[(C1 -C4)alkyl]-amino, R5 is H or (C1 -C4)alkyl and R6 is hydrogen, may be prepared by reacting compounds of the formula II, with compounds of the formulae III, IV and V