Fungicide contg. new or known quinoline cpds.

    公开(公告)号:DE19535208A1

    公开(公告)日:1997-03-27

    申请号:DE19535208

    申请日:1995-09-22

    Applicant: BASF AG

    Abstract: Use of N-(hetero)aryl-hydrazino-quinoline cpds. of formula (I), and their oxides and salts is claimed for combatting fungi. R1-R4 = H, OH, NO2, halo, alkyl, alkoxy, haloalkyl, alkylthio, haloalkoxy, haloalkylthio or alkoxyalkyl; R5, R6 = H, halo, alkyl, alkoxy, haloalkoxy, or alkylthio; R7 = H, alkyl CHO, alkylcarbonyl or alkoxycarbonyl; R8 = H, CHO, 1-8C alkyl, 2-8C alkenyl, 2-8C alkynyl, 1-8C alkylcarbonyl, 3-7C cycloalkyl, 3-7C cycloalkenyl (all opt. partly or fully halogenated) or Ar; or R7+R8 = bond; Ar = aryl or heteroaryl, (both opt. substd. by 1-3 NO2, halo, CN, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylamino, dialkylamino, alkylsulphonyl, alkylsulphoxy, alkylsulphonyloxy, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyl, aryl or aryloxy); R9 = aryl or heteroaryl, (both opt. substd. by 1-3 NO2, halo, CN, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylamino, dialkylamino, alkylsulphonyl, alkylsulphoxy, alkylsulphonyloxy, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyl, aryl or aryloxy, where the cyclic gps. are opt. substd. as in Ar, except for haloalkyl). (I) are new, with exclusions.

    New and known substd. alkylthio-pyridine derivs.

    公开(公告)号:DE19531148A1

    公开(公告)日:1997-02-27

    申请号:DE19531148

    申请日:1995-08-24

    Applicant: BASF AG

    Abstract: Control of fungi using substd. alkylthio-pyridine derivs. (I) and their salts and N-oxides is claimed. R -R = H, CN, NO2 or halo; 1-4C alkyl or 1-4C alkoxy (both opt. substd. by halo), 1-4C alkylthio, 1-4C alkoxy-1-4C alkyl, 1-4C alkoxy-CO or Ar; Ar = aryl, aryloxy or heteroaryl (all opt. ring substd. by 1-3 of halo, CN or NO2; 1-4C alkyl or 1-4C alkoxy (both opt. substd. by halo), 1-4C alkylthio, 1-4C alkoxy-1-4C alkyl, 1-4C alkoxy-CO or 1-4C acyl); m = 0-2; Alk = 1,2-ethylene or 1,3-propylene having any H atom opt. replaced by: (a) alkyl, haloalkyl, alkenyl, haloalkenyl or alkynyl (all having up to 8C and opt. substd. by 1-3 of CN, 1-4C alkoxy (opt. substd. by halo), 1-4C alkylthio, 1-4C alkoxycarbonyl, 3-7C cycloalkyl or 5-7C cycloalkenyl); or (b) 3-7C cycloalkyl or 5-7C cycloalkenyl (both opt. substd. by 1 or more halo or opt. substd. by 1-3 of CN, halo, 1-4C alkyl (opt. substd. by halo) or 1-4C alkoxy); X = O, S or NR ; R = H, 1-8C alkyl or 3-7C cycloalkyl; R = (a) aryl, heteroaryl or aryl-1-4C alkyl (all opt. ring substd. by 1-3 of CN, NO2, halo, 1-4C alkyl or 1-4C alkoxy (opt. substd. by halo), 1-4C alkylthio, 1-4C alkoxy-1-4C alkyl, 1-4C alkoxy-CO, 1-4C alkylsulphinyl, 1-4C alkylsulphonyl, 1-4C acyl or Ar); or (b) 3-7C cycloalkyl or 5-7C cycloalkenyl (both opt. substd. by 1 or more halo or opt. substd. by 1-3 of CN, halo, 1-4C alkyl or 1-4C alkoxy (opt. substd. by halo), 1-4C alkoxy-1-4C alkyl, 1-4C alkylthio, 1-4C alkoxy-carbonyl, 3-7C cycloalkyl, 5-7C cycloalkenyl or Ar).

    SYNERGETIC FUNGICIDE MIXTURES AND THEIR USE

    公开(公告)号:HU225630B1

    公开(公告)日:2007-05-02

    申请号:HU9903739

    申请日:1997-04-22

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP97/02015 Sec. 371 Date Oct. 22, 1998 Sec. 102(e) Date Oct. 22, 1998 PCT Filed Apr. 22, 1997 PCT Pub. No. WO97/40673 PCT Pub. Date Nov. 6, 1997Fungicidal mixtures, comprising a) an oxime ether of the formula I where the substituents have the following meanings: X is oxygen or amino (NH); Y is CH or N; Z is oxygen, sulfur, amino (NH) or C1-C4-alkylamino (N-C1-C4-alkyl); R' is C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-alkenyl, C2-C6-haloalkenyl, C3-C6-alkynyl, C3-C6-haloalkynyl, C3-C6-cycloalkylmethyl, or is benzyl which can be partially or fully halogenated and/or can have attached to it one to three of the following radicals: cyano, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio and/or b) a carbamate of the formula II where T is CH or N, n is 0, 1 or 2 and R is halogen, C1-C4-alkyl or C1-C4-haloalkyl, it being possible for the radicals R to be different if n is 2, and c) a morpholine or piperidine derivative III selected from the group of the compounds IIIa, IIIb and IIIc in a synergistically active amount.

    Fungicidal mixtures based on pyridine carboxamide compounds

    公开(公告)号:SI1201127T1

    公开(公告)日:2004-12-31

    申请号:SI9830657

    申请日:1998-12-15

    Applicant: BASF AG

    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.

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