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    3.
    发明专利
    未知

    公开(公告)号：PT1039800E

    公开(公告)日：2003-02-28

    申请号：PT98965270

    申请日：1998-12-15

    Applicant: BASF AG

    Inventor： HAMPEL MANFRED ,  LORENZ GISELA ,  SCHERER MARIA ,  AMMERMANN EBERHARD ,  STARTHAMNN SIEGFRIED ,  SCHELBERGER KLAUS ,  EICKEN KARL

    IPC: A01N1/00 ,  A01N37/46 ,  A01N43/40 ,  A01N47/12

    Abstract: Fungicidal mixture comprises: (1) an amide compound of formula (I) and (2) one or more compounds (II), (III), (IV) or (V). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a synegistically effective amount of a second component comprising: (a) a carboxamide selected from dimethomorph (IIa) and flumetover (IIb); (b) a valinamide compound of formula (III); (c) at least one compound selected from benalaxyl (IVa), ofurace (IVb), metalaxyl (IVc), furalaxyl (IVd) and oxadixyl (IVe); and/or (d) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethyl-urea (cymoxanil (V)). A = Ar or Het (both optionally substituted by 1-3 alkyl, halo, CHF2, CF3, (halo)alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R = H; R = phenyl (optionally substituted by 1-3 Q and optionally fused to a group M); or cycloalkyl (optionally substituted by 1-3 Q); M = a saturated 5-membered ring which may contain an O or S atom and is optionally substituted by one or more alkyl; Ar = an aryl group; Het = an aromatic or non-aromatic, 5-6 membered heterocycle which contains 1-3 N, O or S atoms; Q = alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl or halo; in Q, the (cyclo)aliphatic residues are optionally halogenated, the cycloaliphatic residues are optionally substituted by 1-3 alkyl, and the phenyl is optionally substituted by 1-5 halo and/or 1-3 (halo)alkyl, (halo)alkoxy or (halo)alkylthio; R = 3-4C alkyl; R = naphthyl, or phenyl (optionally substituted in the 4-position by halo, 1-4C alkyl or 1-4C alkoxy)

    4.
    发明专利
    未知

    公开(公告)号：PT1039807E

    公开(公告)日：2003-01-31

    申请号：PT98966338

    申请日：1998-12-15

    Applicant: BASF AG

    Inventor： LORENZ GISELA ,  EICKEN KARL ,  SCHELBERGER KLAUS ,  HAMPEL MANFRED ,  SCHERER MARIA ,  AMMERMANN EBERHARD ,  STARTHAMNN SIEGFRIED

    IPC: A01N37/34 ,  A01N43/40

    Abstract: Fungicidal mixtures comprise as active componentsa) an amide compound of the formula I in whichA is an aryl group or an aromatic or non-aromatic, 5- or 6-membered heterocycle which has from 1 to 3 hetero atoms which are selected from O, N and S;where the aryl group or the heterocycle may or may not have 1, 2 or 3 substituents which are selected, independently of one another, from alkyl, halogen, CHF2, CF3, alkoxy, haloalkoxy, alkylthio, alkylsulfinyl and alkylsulfonyl;R1 is a hydrogen atom;R2 is a phenyl or cycloalkyl group which may or may not have 1, 2 or 3 substituents which are selected, independently of one another, from alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl and halogen, where the aliphatic and cycloaliphatic radicals may be partially or fully halogenated and/or the cycloaliphatic radicals may be substituted by from 1 to 3 alkyl groups and where the phenyl group may have from 1 to 5 halogen atoms and/or from 1 to 3 substituents which are selected, independently of one another, from alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio and haloalkylthio, and where the amidic phenyl group may or may not be condensed with a saturated 5-membered ring which may or may not be substituted by one or more alkyl groups and/or may have a hetero atom selected from O and S, andb) tetrachloroisophthalonitrile II in a synergistically effective amount.

    6.
    发明专利
    未知

    公开(公告)号：PT1041883E

    公开(公告)日：2003-01-31

    申请号：PT98966339

    申请日：1998-12-15

    Applicant: BASF AG

    Inventor： EICKEN KARL ,  SCHELBERGER KLAUS ,  HAMPEL MANFRED ,  LORENZ GISELA ,  SCHERER MARIA ,  AMMERMANN EBERHARD ,  STARTHAMNN SIEGFRIED

    IPC: A01N43/40 ,  A01N43/84

    Abstract: Fungicidal mixtures comprising as active componentsa) an amide compound of the formula Iin whichA is an aryl group or an aromatic or non-aromatic, 5- or 6-membered heterocycle which has from 1 to 3 hetero atoms selected from O, N and S;where the aryl group or the heterocycle may or may not have 1, 2 or 3 substituents which are selected, independently of one another, from alkyl, halogen, CHF2, CF3, alkoxy, haloalkoxy, alkylthio, alkylsulfynyl and alkylsulfonyl;R is a hydrogen atom;R is a phenyl or cycloalkyl group which may or may not have 1, 2 or 3 substituents which are selected, independently of one another, from alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cyclo-alkenyloxy, phenyl and halogen, where the aliphatic and cycloaliphatic radicals may be partially or fully halogenated and/or the cycloaliphatic radicals may be substituted by from 1 to 3 alkyl groups and where the phenyl group may have from 1 to 5 halogen atoms and/or from 1 to 3 substituents which are selected, independently of one another, from alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio and haloalkylthio, and where the amidic phenyl group may or may not be condensed with a saturated 5-membered ring which may or may not be substituted by one or more alkyl groups and/or may have a hetero atom selected from O and S, andb) a morpholine or piperidine derivative II selected from the group of the compounds IIa, IIb, IIc, IId [sic] and IIe [sic]in a synergistically effective amount.

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