公开(公告)号：BR9910177B1

公开(公告)日：2015-02-10

申请号：BR9910177

申请日：1999-04-23

Applicant: BASF SE

Inventor： SCHELBERGER KLAUS ,  SCHERER MARIA ,  SAUR REINHOLD ,  EICKEN KARL ,  SAUTER HUBERT ,  AMMERMANN EBERHARD ,  GROTE THOMAS ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED

IPC: A01N47/24 ,  A01N37/50 ,  A01N47/12 ,  A01N47/18

Abstract: A fungicidal mixture, comprising at least one compound selected froma) [sic] carbamates of the formula I, in which T is CH or N, n is 0, 1 or 2 and R is halogen, Cl-C4-alkyl or C1-C4-haloalkyl, where the radicals R may be different if n is 2,a2) the oxime ether carboxylate of the formula II ora3) the oxime ether carboxamide of the formula III, andb) a compound of the formula IV where the substituents R1 to R3 have the following meaning:R1 is C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C1-C4-alkyl-C3-C7-cycloalkyl, where these radicals may carry substituents selected from halogen, cyano and Cl-C4-alkoxy,R2 is C1-C4-alkyl or C1-C4-haloalkyl,R3 is hydrogen, halogen, Cl-C4-alkyl, C1-C4-alkoxy, C1-C4-alkylthio, N-C1-C4-alkylamino, Cl-C4-haloalkyl or C1-C4-haloalkoxy,Y is O, S, CHR4 or NR5, where R4 and R5 may each have the meanings mentioned for R2,n is 0, 1, 2 or 3,in a synergistically effective amount, and methods for controlling harmful fungi using these mixtures are described.

公开(公告)号：AU2768397A

公开(公告)日：1997-11-19

申请号：AU2768397

申请日：1997-04-23

Applicant: BASF SE

Inventor： MULLER BERND ,  SAUTER HUBERT ,  AMMERMANN EBERHARD ,  LORENZ GISELA ,  STRATHMANN SIEGFRIED ,  SAUR REINHOLD ,  SCHELBERGER KLAUS ,  LEYENDECKER JOACHIM

IPC: A01N20060101 ,  A01N37/50 ,  A01N37/52 ,  A01N47/24 ,  A01N47/38

Abstract: Synergistic fungicidal mixture comprises: (a) a carbamate of formula (I); and at least one compound selected from: (b) an oxime ether of formula (II); (c) an oxime ether carboxylic acid ester of formula (IIIa), oxime ether carboxylic acid amide of formula (IIIb), methoxyacrylic acid ester of formula (IIIc); (d) an azole derivative (IV) selected from 1-[(2RS,4RS;2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triazole (IVa); 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (IVb); (+)/(-)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-2-yl]phenyl-4-chlorophenylether (IVc); (E)-(R,S)-1-(2,4- dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol(IVd); (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)oxirane (IVe); 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)butyronitrile (IVf); 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4(3H)-one (IVg); bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-ylmethyl)silane (IVh); (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol (IVi); (1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol (IVj); N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazol-1-carboxamide (IVk); (+)/(-)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole (IVl); (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol (IVm); (+)/(-)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazol-1-yl)propyl-1,1,2,2-tetrafluoroethyl ether (IVn); (E)-1-[1[[4-chloro-2-(trifluoromethyl)phenyl]imino]-2-propoxyethyl]-1H-imidazole (IVo); (RS)-2,4'-difluoro-~a-(1H-1,2,4-triazol-1-ylmethyl)benzhydryl alcohol (IVp); 2-p-chlorophenyl-2-(1H-1,2,4-triazol-1-ylmethyl)hexane nitrile (IVq). T = CH or N; n = 0-2; R = halo, 1-4C alkyl or 1-4C haloalkyl; X = O or NH; Y = CH or N; Z = O, S, NH or 1-4C alkylamino; R' = 1-6C alkyl, 1-6C haloalkyl, 3-6C alkenyl, 2-6C haloalkenyl, 3-6C alkynyl, 3-6C haloalkynyl, (3-6C cycloalkyl)methyl or benzyl (optionally substituted by halo and/or 1-3 CN, 1-4C alkyl, 1-4C haloalkyl, 1-4C alkoxy, 1-4C haloalkoxy or 1-4C alkylthio).