55.
    发明专利
    未知

    公开(公告)号:AT136734T

    公开(公告)日:1996-05-15

    申请号:AT94114505

    申请日:1994-09-15

    Applicant: BASF AG

    Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) an azole derivative II selected from the group consisting of the compounds II.1 to II.16 - 1-[(2RS,4RS; 2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triaz ole (II.1) - 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)-butan-2-ol (II.2) - (+/-)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan- 2-yl]-phenyl 4-chlorophenyl ether (II.3) - (E)-(RS)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl) pent-1-ene-3-ol (II.4) - (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophen yl)-oxiran (II.5) - 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)-butyronitrile (II.6) - 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4( 3H)-one (II.7) - bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-ylmethyl)silane (II.8) - (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)-hexan-2-ol (II.9) - (1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H- 1,2,4-triazol-1-ylmethyl)cyclopentanol (II.10) - N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide (II.11) - (+/-)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2 ,4-triazole (II.12) - (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)- pentan-3-ol (II.13) - (+/-)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazolyl)-propyl 1,1,2,2-tetrafluoroethyl ether (II.14) - (E)-1-[1-[[4-chloro-2-(trifluoromethyl)-phenyl]imino]-2-propoxyethyl]- 1H-imidazole (II.15) and - (RS)-2,4'-difluoro- alpha -(1H-1,2,4-triazol-1-ylmethyl)-benzhydryl-alcohol (II.16) in a synergistically active amount.)

    56.
    发明专利
    未知

    公开(公告)号:DK0645091T3

    公开(公告)日:1996-05-13

    申请号:DK94114505

    申请日:1994-09-15

    Applicant: BASF AG

    Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) an azole derivative II selected from the group consisting of the compounds II.1 to II.16 - 1-[(2RS,4RS; 2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triaz ole (II.1) - 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)-butan-2-ol (II.2) - (+/-)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan- 2-yl]-phenyl 4-chlorophenyl ether (II.3) - (E)-(RS)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl) pent-1-ene-3-ol (II.4) - (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophen yl)-oxiran (II.5) - 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)-butyronitrile (II.6) - 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4( 3H)-one (II.7) - bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-ylmethyl)silane (II.8) - (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)-hexan-2-ol (II.9) - (1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H- 1,2,4-triazol-1-ylmethyl)cyclopentanol (II.10) - N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide (II.11) - (+/-)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2 ,4-triazole (II.12) - (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)- pentan-3-ol (II.13) - (+/-)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazolyl)-propyl 1,1,2,2-tetrafluoroethyl ether (II.14) - (E)-1-[1-[[4-chloro-2-(trifluoromethyl)-phenyl]imino]-2-propoxyethyl]- 1H-imidazole (II.15) and - (RS)-2,4'-difluoro- alpha -(1H-1,2,4-triazol-1-ylmethyl)-benzhydryl-alcohol (II.16) in a synergistically active amount.)

    New fungicidal cpds. used for plant protection

    公开(公告)号:DE4437496A1

    公开(公告)日:1996-04-25

    申请号:DE4437496

    申请日:1994-10-20

    Applicant: BASF AG

    Abstract: Carbamoyl carboxylic acid amide derivs. of formula (I) and their salts are new. R1 = R or N=CW1W2; R = 1-8C alkyl, 2-8C alkenyl or 2-8C alkynyl, 3-7C cycloalkyl, 3-7C cycloalkenyl, A', aryl or heteroaryl (all opt. substd.), N=CW1W2; A' = a non-aromatic 4-8 membered ring (opt. contg. 1 or 2 heteroatoms); W1 = R; W2 = H or R; R2, R5 = H, 1-8C alkyl or 3-7C cycloalkyl (these last 2 gps. opt. partially or completely halogenated); R3 = 1-8C alkyl, 3-7C cycloalkyl, (opt. substd.); R4 = H or R3; or CR3R4 = A'; X = independently 1-8C alkyl, 2-8C alkenyl, 3-7C cycloalkyl and/or 3-7C cycloalkenyl (all opt. substd.) or H; m = 0-2; A = =CY1Y2; Y1 = 3-7C cycloalkyl or 3-7C cycloalkenyl (both opt. substd.); Y2 = 1-8C alkyl, 2-8C alkenyl or aryl (all opt. substd.), Y1 or H; R6 = aryl or heteroaryl (both opt. substd.)

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