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    Fungicide mixtures based on pyridine amides or thiazole amides or pyrazole amides, and chlorothalonil (tetrachloroisophthalonitrile)
    133.
    发明专利
    Fungicide mixtures based on pyridine amides or thiazole amides or pyrazole amides, and chlorothalonil (tetrachloroisophthalonitrile) 未知

    公开(公告)号：NZ505623A

    公开(公告)日：2003-02-28

    申请号：NZ50562398

    申请日：1998-12-15

    Applicant: BASF AG

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

    IPC: A01N37/34 ,  A01N43/40 ,  A01N43/78 ,  A01N43/56

    Abstract: A fungicidal composition comprising as active components: an amide compound of formula I A-CO-NR1R2 (I) wherein: A is pyridyl, thiazolyl or pyrazolyl, where these groups optionally have 1, 2 or 3 substituents selected from alkyl, halogen, difluoromethyl or trifluoromethyl; R1 is hydrogen; R2 is phenyl, which optionally has 1, 2 or 3 substituents selected from alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl or halogen, where the aliphatic and cycloaliphatic radicals are unsubstituted or partially or fully halogenated, the cycloaliphatic radicals are optionally substituted by from 1 to 3 alkyl groups, and the phenyl group optionally has from 1 to 5 halogen atoms and/or from 1 to 3 substituents selected from alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio or haloalkylthio, and where the amidic phenyl group is optionally condensed with a saturated 5-membered ring which is optionally substituted by one or more alkyl groups, and /or optionally has a hetero atom selected from O, S or a cycloalkyl group which optionally has 1-3 alkyl groups.

    СИНЕРГЕТИЧЕСКИЕ ФУНГИЦИДНЫЕ СМЕСИ НА ОСНОВЕ ПРОИЗВОДНЫХ N-ФЕНИЛНИКОТИНАМИДА И АЗОЛОВ
    134.
    发明专利
    СИНЕРГЕТИЧЕСКИЕ ФУНГИЦИДНЫЕ СМЕСИ НА ОСНОВЕ ПРОИЗВОДНЫХ N-ФЕНИЛНИКОТИНАМИДА И АЗОЛОВ 未知

    公开(公告)号：EA003136B1

    公开(公告)日：2003-02-27

    申请号：EA200000676

    申请日：1998-12-15

    Applicant: BASF AG

    Inventor： SCHELBERGER KLAUS ,  SCHERER MARIA ,  EICKEN KARL ,  HAMPEL MANFRED ,  AMMERMAN EBERHARD ,  LORENZ GISELLA

    IPC: A01N37/22 ,  A01N37/24 ,  A01N43/08 ,  A01N43/16 ,  A01N43/32 ,  A01N43/40 ,  A01N43/56 ,  A01N43/653 ,  A01N43/76 ,  A01N43/78 ,  A01N47/38 ,  A01N55/00 ,  A01N43/50

    Abstract: Визобретенииописанафунгициднаясмесь, содержащаяв качествеактивныхкомпонентова) амидноесоединениеформулы Iбгде RозначаетгалогениRозначаетфенил, замещенныйгалогеном; иб) производноеазолов II, выбранноеизгруппы, включающейсоединения II.1-II.17:1-[(2RS,4RS;2RS,4SR)-4-бром-2-(2,4-дихлорфенил)тетрагидрофурил]-1Н-1,2,4-триазол (II.1);2-(4-хлорфенил)-3-циклопропил-1-(1Н-1,2,4-триазол-1-ил)бутан-2-ол (II.2);(±)-4-хлор-4-[4-метил-2-(1Н-1,2,4-триазол-1-илметил)-1,3-диоксолан-2-ил]фенил-4-хлорфениловыйэфир (II.3);(Е)-(R,S)-1-(2,4-дихлорфенил)-4,4-диметил-2-(1Н-1,2,4-триазол-1-ил)пент-1-ен-3-ол (II.4);(Z)-2-(1Н-1,2,4-триазол-1-илметил)-2-(4-фторфенил)-3-(2-хлорфенил)оксиран (II.5);4-(4-хлорфенил)-2-фенил-2-(1Н-1,2,4-триазолметил)бутиронитрил (II.6);3-(2,4-дихлорфенил)-6-фтор-2-(1Н-1,2,4-триазол-1-ил)хиназолин-4(3Н)-он (II.7);бис(4-фторфенил)(метил)(1Н-1,2,4-триазол-1-илметил)силан (II.8);(R,S)-2-(2,4-дихлорфенил)-1-(1Н-1,2,4-триазол-1-ил)гексан-2-ол (II.9);(1RS,5RS;1RS,5SR)-5-(4-хлорбензил)-2,2-диметил-1-(1Н-1,2,4-триазол-1-илметил)цикпопентанол (II.10);N-пропил-N-[2-(2,4,6-трихлорфенокси)этил]имидазол-1-карбоксамид (II.11);(±)-1-[2-(2,4-дихлорфенил)-4-пропил-1,3-диоксолан-2-илметил]-1Н-1,2,4-триазол (II.12);(R,S)-1-(4-хлорфенил)-4,4-диметил-3-(1Н-1,2,4-триазол-1-илметил)пентан-3-ол (II.13);(±)-2-(2,4-дихлорфенил)-3-(1Н-1,2,4-триазолил)пропил-1,1,2,2-тетрафторэтиловыйэфир (II.14) и(Е)-1-[1-[[4-хлор-2-(трифтормтеил)фенил]имино]-2-пропоксиэтил]-1Н-имидазол (II.15);(R,S)-2,4'-дифтор-α-(1Н-1,2,4-триазол-1-илметил)бензгидриловыйспирт (II.16);2-п-хлорфенил-2-(1Н-1,2,4-триазол-1-илметил)гексаненитрил (II.17)всинергетическиэффективномколичестве.Крометого, описанспособборьбыс фитопатогеннымигрибами, характеризующийсятем, чтогрибы, ихпространствопроизрастанияилиподлежащиезащитеотпораженияимиматериалы, растения, почву, семена, поверхностиилипомещенияобрабатываютфунгициднойсмесьюпоодномуизпп.1-3, причемдействующиевещества, аименноамидноесоединениеформулы Iби азолформул II.1-II.17, применяютодновременно, аименносовместноилираздельно, илипоследовательно.

    139.
    发明专利
    未知

    公开(公告)号：AT227078T

    公开(公告)日：2002-11-15

    申请号：AT98966621

    申请日：1998-12-15

    Applicant: BASF AG

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

    IPC: A01P3/00 ,  A01N37/52 ,  A01N43/00 ,  A01N43/34 ,  A01N43/40 ,  A01N43/42

    Abstract: Fungicidal mixtures comprise: (1) an amide compound of formula (I) and (2) a quinoline derivative of formula (II) and/or an amine compound of formula (III). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a synergistically effective amount of a second component which comprises: (i) a quinoline derivative of formula (II), or an N-oxide or salt and/or; (ii) a compound of formula (III). 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 -R = H, OH, NO2, halo, T, TO or TS; R -R = H, OH, CN, NO2, halo, R, RO, RS, 1-7C hydroxyalkyl, 2-4C acyl, or aryl or aryloxy (both optionally substituted by 1-3 CN, NO2, halo, T, TO or TS); X -X = H, halo, T, TO, 1-4C alkylthio, 1-4C thioalkoxy, 1-4C sulfonylalkyl, NO2, NH2, N-(1-4C carboxyl)-amino or N-(1-4C alkyl)-amino; R = 1-4C alkyl, 2-4C alkenyl, 2-4C alkynyl or 1-4C alkyl-(3-7C) cycloalkyl (all optionally substituted by halo, CN or 1-4C alkoxy); R = phenyl or Het' (both optionally substituted by halo, T, TO, 1-4C alkoxy-(2-4C) alkenyl or 1-4C alkoxy-(2-4C) alkynyl; R , R = H, T, TO, 1-4C alkylthio or N-(1-4C alkyl)-amino T = 1-4C alkyl, halo(1-4C)alkyl; R = 1-7C alkyl, halo(1-7C)alkyl.

    Fungicide mixtures based on amide compounds and morpholine or piperidine derivatives
    140.
    发明专利
    Fungicide mixtures based on amide compounds and morpholine or piperidine derivatives 未知

    公开(公告)号：AU754335B2

    公开(公告)日：2002-11-14

    申请号：AU2054099

    申请日：1998-12-15

    Applicant: BASF AG

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

    IPC: A01N1/00 ,  A01N37/46 ,  A01N43/40 ,  A01N47/12 ,  A01N43/84 ,  A01N37/18

    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)

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