FUNGICIDAL MIXTURE AND A METHOD OF CONTROLLING PHYTOPATHOGENIC FUNGI

    公开(公告)号:UA72490C2

    公开(公告)日:2005-03-15

    申请号:UA2001075221

    申请日:1999-12-11

    Applicant: BASF AG

    Abstract: The invention relates to fungicide mixtures containing the following as their active components: a compound of formula (I) (І), its N-oxide or one of its salts, wherein the radicals have the following meanings: R1, R2, R3 and R4, independently of each other, represent hydrogen, hydroxy, nitro, halogen, С1-C4-alkyl, С1-C4-alkyl halide, С1-C4-аlkоху, С1-C4-halogenalkoxy, С1-C4-alkylthio and С1-C4-halogenalkylthio; R5, R6 and R7 independently of each other, represent hydrogen, hydroxy, cyano, nitro, С1-C7-alkyl, С1-C7-alkyl halide, С1-C7-alkoxy, С1-C7-halogenalkoxy, С1-C7-alkylthio, С1-C7-halogenalkylthio, С1-C7-hydroxyalkyl, С2-С4-acyl, aryl and aryloxy and the radicals with aryl can carry one to three of the following groups: cyano, nitro, halogen, С1-C4-alkyl, С1-C4-alkyl halide, С1-C4-alkoxy, С1-C4-halogenalkoxy, С1-C4-alkylthio and С1-C4-halogenalkylthio; and b) carbamates of formula (II) (ІІ), wherein Τ means CH or Ν, n stands for 0, 1 or 2 and R means halogen, С1-C4-alkyl or С1-C4-alkyl halide and the radicals R can be different when n stands for 2, in a synergistically effective quantity.

    116.
    发明专利
    未知

    公开(公告)号:IN835CH1997A

    公开(公告)日:2005-03-04

    申请号:IN835CH1997

    申请日:1997-04-23

    Applicant: BASF AG

    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).

    Fungicidal traizolopyrimidines, method for the production thereof and use thereof in controlling noxious fungi and agents containing said compounds.

    公开(公告)号:ZA200400914B

    公开(公告)日:2005-02-04

    申请号:ZA200400914

    申请日:2004-02-04

    Applicant: BASF AG

    Abstract: 5-(Alkyl, alkenyl or alkynyl)-7-(hydrocarbyl or heterocyclyl)-6-phenyl-1,2,4-triazolo[1,5-a]pyrimidines (I) are new. 5-(Alkyl, alkenyl or alkynyl)-7-(hydrocarbyl or heterocyclyl)-6-phenyl-1,2,4-triazolo[1,5-a]pyrimidines of formula (I) are new. [Image] n : 0-5; R : halo, CN, OH or OCN, or alkyl, alkenyl, alkynyl, T', haloalkenyl, OT, alkenyloxy, alkynyloxy, OT', cycloalkyl, cycloalkenyl, cycloalkoxy, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, CONH 2, mono- or dialkylaminocarbonyl, alkoximinoalkyl, alkenyloximinocarbonyl, alkynyloximinoalkyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, cycloalkylcarbonyl or Het (all optionally partially or completely halogenated and optionally substituted by 1-4 R a); T : 1-6C alkyl; T' : 1-6C haloalkyl; Het : 5-10 membered, saturated, partially unsaturated or aromatic heterocycle containing 1-4 of O, N and/or S heteroatoms; R 11-10C alkyl, alkenyl, alkynyl, 3-12C cycloalkyl, 3-10C cycloalkenyl, phenyl, naphthyl or Het (all optionally partially or completely halogenated and optionally substituted by 1-4 R a); R ahalo, CN, NO 2, OH, T, T', COT, cycloalkyl, OT, OT', COOT, NHT, NT 2, 2-6C alkenyl, 2-6C alkenyloxy, 3-6C alkynyloxy, alkoximino, alkenyloximino, alkynyloximino, aralkoximino, alkynyl, alkynyloxycarbonyl, phenyl, naphthyl or Het (where all aliphatic, alicyclic or aromatic groups are optionally partially or completely halogenated and optionally substituted by 1-3 R aand/or 1-3 R c); R bhalo, CN, NO 2, OH, SH, NH 2, COOH, CONH 2, CSNH 2, T, T', 2-8C alkenyl, 2-8C alkenyloxy, 2-8C alkynyloxy, OT, OT', ST, NHT, NT 2, CHO, COT, SO 2T, SOT, COOT, OCOT, CONHT, CONT 2, CSNHT or CSNT 2; R ccycloalkyl, -O-cycloalkyl, heterocyclyl, -O-heterocyclyl, aryl, -O-aryl, -S-aryl, -O-T-aryl, -T-aryl, heteroaryl, -O-heteroaryl or -S-heteroaryl (where cycloalkyl or heterocyclyl rings are 3-10 membered, aryl rings are preferably 6-10 membered and heteroaryl rings are preferably 5-6 membered; and all rings are optionally partially or completely halogenated and optionally substituted by alkyl or haloalkyl); and R 21-4C alkyl, 2-4C alkynyl or 2-4C alkynyl (all optionally substituted by halo, CN, NO 2, OMe, OEt or 1-4C alkoxycarbonyl; Unless specified otherwise alkyl moieties have 1-8C, alkenyl or alkynyl moieties 2-10C and cycloalkyl or cycloalkenyl moieties 3-6C. Independent claims are also included for: (1) preparation of (I); and (2) dicarbonyl compound intermediates of formula (III), provided that n is not 0 and R 1and R 2are not both Me. [Image] ACTIVITY : Fungicide. 7-Cyclohexyl-5-methyl-6-(2-chloro-6-fluorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine (Ia) at a concentration of 63 ppm gave at least 90 % protection of tomato plants against Alternaria solani. MECHANISM OF ACTION : None given.

    119.
    发明专利
    未知

    公开(公告)号:BR0308831A

    公开(公告)日:2005-01-25

    申请号:BR0308831

    申请日:2003-04-02

    Applicant: BASF AG

    Abstract: The invention relates to a fungicidal mixture containing (1) a benzamidoxime derivative of formula (I), whereby the substituent and the index are defined as follows: R represents hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy or C 1 -C 4 haloalkoxy, n represents 1, 2 or 3; and at least one additional strobilurin derivative, selected from (2) a trifloxystrobin of formula (II), or (3) a picoxystrobin of formula (III), or (4) a pyraclostrobin of formula (IV), or (5) a strobilurin derivative of formula (V), or (6) a strobilurin derivative of formula (VI), or (7) a dimoxystrobin of formula (VII), or (8) a kresoxim methyl of formula (VIII), or (9) an azoxystrobin of formula (IX), or (10) a strobilurin derivative of formula (X) in a synergistically active quantity.

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