FUNGICIDE MIXTURES WHICH ARE BASED ON DERIVATIVES OF MORPHOLINE OR PIPERIDINE AND DERIVATIVES OF OXIME ETHER

    公开(公告)号:CA2356114C

    公开(公告)日:2009-05-05

    申请号:CA2356114

    申请日:1999-12-11

    Applicant: BASF AG

    Abstract: The invention relates to fungicide mixtures containing the following as their active components: a) a morpholine or piperidine derivative (I) chosen from the following group of compounds (Ia), (Ib), (Ic) and (Id) and compounds of formula (II), the substituents X1 to X5 and R1 to R4 having the following meanings: X1 C1-C4 represents alkyl halide, C1-C4 represents halogenalkoxy or halogen; X1 to X5 represent, independently of each other, hydrogen, halogen, C1-C4-alkyl, C1-C4-alkyl halide, C1-C4-alkoxy or C1-C4-halogenalkoxy; R1 represents C1-C4-alkyl, C2-C6-alkenyl, C2-C6-alkinyl, C1-C4 alkyl-C3-C7-cycloalkyl, C1-C4-alkyl-C3-C7-cycloalkenyl, and these radicals can carry substituents chosen from the following: halogen, cyano and C1-C4-alkoxy; R2 represents a phenyl radical or a 5- or 6-membered saturated or unsaturated heterocyclyl radical with at least one hetero atom chosen from the following group: N, O and S; the cyclical radicals having one to three substituents chosen from the following group: halogen, C1-C4-alkyl, C1-C4 alkoxy, C1-C4-alkyl halide, C1-C4-halogenalkoxy, C1-C4-alkoxy-C2-C4alkenyl, C1-C4-alkoxy-C2-C4-alkinyl; R3 and R4 represent, independently of each other, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-alkylthio, N-C1-C4 alkylamino, C1-C4-alkyl halide or C1-C4-halogenalkoxy in a synergistically effective quantity.

    63.
    发明专利
    未知

    公开(公告)号:DE50309022D1

    公开(公告)日:2008-03-06

    申请号:DE50309022

    申请日:2003-03-19

    Applicant: BASF AG

    Abstract: The invention relates to triazolopyrimidines of formula (I), in which the substituents are defined as follows: L 1 represents cyano, S(-O) n A 1 or C(-O)A 2 , wherein A 1 stands for hydrogen, hydroxy, alkyl, alkylamino or dialkylamino; A 2 stands for C 1 -C 8 alkoxy, C 1 -C 6 haloalkoxy or one of the groups named in A 1 ; and n stands for 0, 1 or 2; L 2 , L 3 represent hydrogen or halogen; L 4 , L 5 represent hydrogen, halogen or alkyl; X represents halogen, cyano, alkyl, haloalkyl, alkoxy or haloalkoxy; R 1 represents alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, alkadienyl, haloalkenyl, cycloalkenyl, alkynyl, haloalkynyl or cycloalkynyl, phenyl, naphthyl, or a five to ten-membered saturated, partially unsaturated or aromatic heterocyclus containing between one and four heteroatoms from the group containing O, N or S; R 2 represents hydrogen or R 1 ; R 1 and R 2 can form, together with the nitrogen atom to which they are bonded, a five or six-membered ring, which can be interrupted and/or substituted by an atom from the group O, N and S; whereby R 1 and/or R 2 can be substituted in accordance with the description. The invention also relates to methods and intermediate products for producing said compounds, to agents containing the latter and to the use of said compounds for combating harmful fungi.

    68.
    发明专利
    未知

    公开(公告)号:DK1489906T3

    公开(公告)日:2007-10-01

    申请号:DK03712051

    申请日:2003-03-19

    Applicant: BASF AG

    Abstract: A new fungicidal mixture contains synergistic amounts of (1) prothioconazole (I) and (2) at least one of 20 other specific fungicides, e.g. boscalid, carboxine, metrafenone, quinoxyfen, fenoxanil, carbendazim, metalaxyl, prochloraz or anthraquinone. A fungicidal mixture contains synergistic amounts of the following active components: (1) prothioconazole (I) or its salt or adduct; and (2) one or more of boscalid, carboxine, metrafenone, N-(alpha -cyclopropoxyimino)-(2,3-difluoro-6-trifluoromethyl-benzyl)-phenylacetamide, N-(alpha -cyclopropoxyimino)-2,3-difluoro-6-difluoromethyl-benzyl)-phenylacetamide, quinoxyfen, dithianon, thiram, mepiquat chloride, cyazofamid, fenoxanil, 6-fluoro-2-(1-(2-(isopropoxycarbonylamino)-isovaleramido)-ethyl)-benzothiazole, thiophanate methyl, carbendazim, metalaxyl, fludioxonil, thiabendazole, quintozen, prochloraz and/or anthraquinone. Independent claims are included for: (a) a harmful fungus control method involving application of the mixture of (1) and (2) to the fungi, their habitat or plants, seeds, soil, surfaces, materials or regions to be protected ((1) and (2) being applied simultaneously, separately or successvely); and (b) a fungicidal composition comprising the (1)/(2) mixture together with a solid or liquid carrier. ACTIVITY : Fungicide. In tests for protective action against Blumeria graminis f. sp. triciti (mildew) in wheat, prothioconazole (I) at 1 ppm alone or boscalid (II) at 4 ppm alone gave no (0%) control, whereas a combination of 1 ppm (I) and 4 ppm (II) gave 92% control. MECHANISM OF ACTION : None given in the source material.

    FUNGICIDE MIXTURES BASED ON PYRIDINE AMIDES AND FENARIMOL

    公开(公告)号:CA2313323C

    公开(公告)日:2007-09-04

    申请号:CA2313323

    申请日:1998-12-15

    Applicant: BASF AG

    Abstract: The invention relates to fungicide mixtures containing, as active components, a) an amide compound of formula (I) A-CO-NR1R2, wherein A represents an aryl group or an aromatic or non-aromatic, 5- or 6-structured heterocyclic compound having 1 to 3 heteroatoms selected from O, N, S; whereby the aryl group or the heterocycli c compound can optionally comprise 1, 2 or 3 substituents selected independently of one another from alkyl, halogen, CHF2, CF3, alkoxy l, haloalkoxyl, alkylthio, alkyl sulfinyl and alkyl sulfonyl; R1 represents a hydrogen atom; R2 represents a phenyl group or cycloalkyl group optionally containing 1, 2 or 3 substituents selected independently of one another from alkyl, alkenyl, alkynyl, alkoxyl, alkenyloxyl, alkynyloxyl, cycloalkyl, cycloalkenyl, cycolalkyloxyl, cycloalkenyloxyl, phenyl and halogen, whereby the aliphatic and cycloaliphat ic radicals can be partially or completely halogenated and/or the cycloaliphatic radicals can be substituted by 1 to 3 alkyl groups, where by the phenyl group can contain 1 to 5 halogen atoms and/or 1 to 3 substituents selected independently of one another from alkyl, haloalky l, alkoxyl, haloxyl, alkylthio and haloalkylthio, and whereby the amidic phenyl group is optionally condensed with a saturated 5-structured ri ng which is optionally substituted by one or more alkyl groups and/or can comprise a heteroatom selected from O and S, and b) (~)-(2- chlorphenyl)(4-chlorphenyl)(pyrimidine-5-yl)methanol (a). The active components are provided in a synergistically effective quantity.

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