Herbicidal mixtures having a synergistic effect

    公开(公告)号:AU4608999A

    公开(公告)日:2000-01-05

    申请号:AU4608999

    申请日:1999-06-12

    Applicant: BASF AG

    Abstract: A synergistic herbicidal mixture comprising A) at least one compound of the formula I wherein R1, R3 are hydrogen, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, alkylsulfinyl or alkylsulfinyl; R2 is optionally substituted thiazol-2-yl, thiazol-4-yl, thiazol-5-yl, isoxazol-3-yl, isoxazol-4-yl, isoxazol-5-yl, 4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl, 4,5-dihydroisoxazol-5-yl; R4 is hydrogen, halogen or alkyl; R5 is alkyl; R6 is hydrogen or alkyl; or one of its environmentally compatible salts; and B) a synergistically effective amount of at least one herbicidal compound from the group of ACC inhibitors, ALS inhibitors, amides, aixin herbicides, auxin transport inhibitors, carotenoid biosynthesis inhibitors, ESPS inhibitors, glutamine synthetase inhibitors, lipid biosynthesis inhibitors, mitosis inhibitors, protoporphyrinogen IX oxidase inhibitors, photosynthesis inhibitors, synergists, growth substances, cell wall biosynthesis inhibitors and a variety of other herbicides. Compositions comprising these mixtures, processes for the preparation of these compositions, and their use for controlling undesired plants.

    Substituted (4-brompyrazole-3-yl)benzazoles

    公开(公告)号:AU3820299A

    公开(公告)日:1999-11-16

    申请号:AU3820299

    申请日:1999-04-22

    Applicant: BASF AG

    Abstract: Substituted (4-bromopyrazol-3-yl)benzazoles Iand their salts whereR1=H, C1-C4-alkyl, C1-C4-haloalkyl;R2=CN, Cl-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C1-C4-alkylthio, C1-C4-haloalkylthio, C1-C4-alkylsulfinyl, C1-C4-haloalkylsulfinyl, C1-C4-alkylsulfonyl, C1-C4-haloalkylsulfonyl;R4=H, halogen;R5=H, CN, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy or C1-C4-haloalkoxy;Z=-N=C(XR6)-O- or -N=C(XR6)-S-, attached to alpha via the nitrogen, oxygen or sulfur;X=a chemical bond, oxygen, sulfur, -S(O)-, -SO2-, -NH- or -N(R7)-;R6, R7=Cl-C6-alkyl, Cl-C6-haloalkyl, cyano-Cl-C4-alkyl, hydroxy-C1-C4-alkyl, C3-C6-alkenyl, cyano-C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkynyl, cyano-C3-C6-alkynyl, C3-C6-haloalkynyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-haloalkoxy-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkynyloxy-C1-C4-alkyl, C3-C8-cycloalkyloxy-C1-C4-alkyl, amino-Cl-C4-alkyl, C1-C4-alkylamino-C1-C4-alkyl, di(C1-C4-alkyl)amino-C1-C4-alkyl, Cl-C4-alkylthio-C1-C4-alkyl, C1-C4-haloalkylthio-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3-C4-alkynylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-Cl-C4-alkyl, C1-C4-haloalkylsulfinyl-C1-C4if X=a chemical bond, -O-, -S-, -NH- or -N(R7)-, R6 may also be C1-C4-alkylcarbonyl, C1-C4-haloalkylcarbonyl, C1-C4-alkoxycarbonyl, C1-C4-alkylsulfonyl or C1-C4-haloalkylsulfonyl;if X=a chemical bond, R6 may furthermore be CN, SH, NH2, halogen, -CH2-CH(halogen)-R8, -CH=CH-R8 or -CH=C(halogen)-R8, where R8=COOH, C1-C4-alkoxycarbonyl, C1-C4-alkylthiocarbonyl, CONH2, C1-C4-alkylaminocarbonyl, di(C1-C4-alkyl)aminocarbonyl or di(C1-C4-alkyl)phosphonyl;or R6+R7=an unsubstituted or substituted 1,3-propylene, tetramethylene, pentamethylene or ethyleneoxyethylene chain.Use: As herbicides; for the desiccation/defoliation of plants.

    99.
    发明专利
    未知

    公开(公告)号:TR199901665T2

    公开(公告)日:1999-09-21

    申请号:TR9901665

    申请日:1998-01-08

    Applicant: BASF AG

    Abstract: 4-(3-Heterocyclyl-benzoyl)-pyrazole derivatives (I) and their salts are new: R1, R3 = H; NO2; halo; CN; 1-6C alkyl, 1-6C alkoxy, 1-6C alkylthio, 1-6C alkylsulphinyl or 1-6C alkylsulphonyl optionally substituted by halo; H2NSO2; (1-6C alkyl)NHSO2; (1-6C alkyl)2NSO2; (1-6C alkyl)SO2NH-; (1-6C haloalkyl-SO2)NH-; (1-6C alkyl)(1-6C alkyl-SO2)N-; or (1-6C haloalkyl)(1-6C alkyl-SO2)N-; R2 = optionally substituted 5- or 6-membered heterocycle containing 1-4 O, S and/or N atoms; R6 = 1-6C alkyl; R7 = 1-6C alkyl; 3-6C alkenyl or 3-6C alkynyl optionally substituted by halo; 3-6C cycloalkyl; 1-6C alkylcarbonyl; 2-6C alkenylcarbonyl; 2-6C alkynylcarbonyl; 3-6C cycloalkylcarbonyl; 1-6C alkoxycarbonyl; 3-6C alkenyloxycarbonyl; 3-6C alkynyloxycarbonyl; 1-6C alkyl-NH-CO-; 3-6C alkenyl-NH-CO-; 3-6C alkynyl-NH-CO-; (1-6C alkyl)2N-CO-; (3-6C alkenyl)(1-6C alkyl)N-CO-carbonyl; (3-6C alkynyl)(1-6C alkyl)N-CO-; (1-6C alkoxy)(1-6C alkyl)N-CO-; (3-6C alkenyl)(1-6C alkoxy)N-CO-; (3-6C alkynyl)(1-6C alkoxy)N-CO-; (1-6C alkyl)2N-CS-; 1-6C alkoxyimino-1-6C alkyl; 1-6C alkylamino imino-1-6C alkyl; or di(1-6C alkylamino)imino-1-6C alkyl (alkyl, cycloalkyl and alkoxy groups are optionally substituted by 1 or more halo and/or by 1-3 CN, OH, 1-4C alkoxy, 1-4C alkylthio, di(1-4C alkyl)amino, 1-4C alkylcarbonyl, 1-4C alkoxycarbonyl, 1-4C alkoxy-1-4C alkoxycarbonyl, (1-4C alkyl)2N-1-4C alkoxycarbonyl, COOH, 1-4C alkyl-NH-CO-, (1-4C alkyl)2N-CO-, CONH2; 1-4C alkylcarbonyloxy or 3-6C cycloalkyl); or Ar; Ar-1-6C alkyl; Ar-CO-1-6C alkyl; Ar-CO-; Ar-O-CO-; Ar-NH-CO-; (1-6C alkyl)(Ar)N-CO-; or Ar-2-6C alkenylcarbonyl; Ar = phenyl or heterocyclyl optionally substituted by 1 or more halo and/or by 1-3 NO2, CN or 1-4C alkyl or 1-4C alkoxy (optionally substituted by halo), and R8 = H, 1-6C alkyl or 1-6C haloalkyl.

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