Abstract:
The invention relates to benzyl amidoxime derivatives of formula (I) as fungicides wherein: A represents an aryl or heteraryl radical; Y represents a straight-chained or branched C1-C4 alkylene group, whereby a carbon atom can be substituted by an oxygen, nitrogen or sulphur atom or by a cyclopropyl group; Rn represents one to five similar or different radicals from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 halogen alkyl, C1-C4 halogen alkoxy, C1-C4 alkylthio, C1-C4 alkoxyalkoxy; R represents optionally substituted phenyl C1-C6 alkyl, thienyl C1-C4 alkyl, or pyrazolyl C1-C4 alkyl, Rp represents one to five similar or different radicals from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 halogen alkyl, C1-C4 halogen alkoxy, C1-C4 alkylthio, C1-C4 alkoxyalkoxy, C1-C6 alkyl carbonyl; n represents 0-5; and p represents 0-4, according to the number of free valences.
Abstract:
The present invention relates to compounds of the general formula (I) and to the salts thereof, wherein the substituents and the n index have the following values: Q represents -C(=CHCH3)-COOCH3, -C(=CHOCH3)-COOCH3, -C(=NOCH3)-COOCH3 or -C(=NOCH3)-CONH(CH3); R represents hydrogen, halogen, C1-C4 alkyl, C1-C2 halogenalkyl, C1-C4 alkoxy or C1-C2 halogenalkoxy; R represents halogen, C1-C4 alkyl, C1-C2 halogenalkyl or C1-C4 alkoxy; n is 0, 1 or 2, wherein the R substituents can be different when n = 2; and R represents phenyl, pyridyle or pyrimidyle. This invention also relates to agents containing these compounds as well as to the use of said compounds (I) and agents against noxious fungi and animal parasites.
Abstract translation:通式(I)和它们的盐,其中取代基和指数n具有以下含义的化合物:Q是-C(= CHCH 3)-COOCH 3,-C(= CHOCH 3)-COOCH 3,C(= NOCH 3) - COOCH 3或-C(= NOCH 3)-CONH(CH 3); R 1是氢,卤素,C 1 -C 4烷基,C 1 -C 2卤代烷基,C 1 -C 4烷氧基或C 1 -C 2卤代烷氧基; R 2是卤素,C 1 -C 4烷基,C 1 -C 2卤代烷基,C 1 -C 4烷氧基; n是0,1或2,其中当n = 2时取代基R 2可以不同; R 3苯基,吡啶基或嘧啶基,含有它们的试剂以及化合物(I)和防治有害真菌和动物害虫的试剂的用途。
Abstract:
The invention relates to fungicide mixtures containing, as active components, a) an amide compound of formula (I) A-CO-NR R wherein A, R and R have the meanings given in the description, and b) dimethomorph or flumetover, and/or c) a valine amide of formula (III) wherein R represents C3-C4-alkyl and R represents naphthyl or phenyl, whereby the phenyl radical is substituted by a halogen atom, a C1-C4-alkyl- or a C1-C4-alkoxyl group in 4-position, and/or d) benalaxyl, ofurace, metalaxyl, furalaxyl, or oxydixyl, and/or e) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethyl urea. The active components are provided in a synergistically effective quantity.
Abstract:
The invention relates to fungicide mixtures containing, as active components, a) an amide compound of formula (I) A-CO-NR R and b) a dithiocarbamate (II) selected from the group: manganese-ethylene bis(dithiocarbamate) (zinc complex) (IIa); manganese-ethylene bis(dithiocarbamate) (IIb); zinc ammoniate-ethylene bis(dithiocarbamate) (IIc) and zinc-ethylene bis(dithiocarbamate) (IId), and/or c) a carbamate of formula (III) (CH3)2N-CH2CH2CH2-NH-CO2-CH2CH2CH3 and/or b) a N-acetonyl-benzamide of formula (IV) or one of the salts thereof or adducts, and/or b) an active substance of formula (V), and/or an active substance of formula (VI), and/or e) an active substance of formula (VII), whereby the substituents have the meanings given in the description. The active components are provided in a synergistically effective quantity.
Abstract:
Phenyl acetic acid derivatives of formula (I) in which the substituents and index have the following meanings: X is oxygen or sulphur; R is hydrogen and alkyl; R is hydrogen and alkyl; R is cyano, nitro, trifluoromethyl, halogen, alkyl and alkoxy; m is 0, 1 ou 2, in which the radicals R may be different if m is 2; R is hydrogen, cyano, nitro, hydroxy, amino, halogen, alkyl, halogen alkyl, alkoxy, halogen alkoxy, alkylthio, alkylamino or dialkylamino; R is hydrogen, cyano, nitro, hydroxy, amino, halogen, possibly substituted alkyl, alkoxy, alkylthio, alkylamino, dialkylamino, alkenyl, alkenyloxy, alkenylthio, alkenylamino, N-alkenyl-N-alkylamino, alkinyl, alkinyloxy, alkinylthio, alkinylamino, N-alkinyl-N-alkylamino; optionally substituted cycloalkyl, cycloalkyloxy, cycloalkylthio, cycloalkylamino, N-cycloalkyl-N-alkylamino, cycloalkenyl, cycloalkenyloxy, cycloalkenylthio, cycloalkenylamino, N-cycloalkenyl-N-alkylamino, heterocyclyl, heterocyclyloxy, heterocyclylthio, heterocyclylamino, N-heterocylcyl-N-alkylamino, aryl, aryloxy, arylthio, arylamino, n-aryl-n-alkylamino, hetaryl, hetaryloxy, hetarylthio, hetarylamino, N-hetaryl-N-alkylamino; R is hydrogen, optionally substituted alkyl, cycloalkyl, alkenyl, alkinyl, alkylcarbonyl, alkenylcarbonyl, alkinylcarbonyl or alkylsulfonyl; optionally substituted aryl, arylcarbonyl, arylsulfonyl, hetaryl, hetarylcarbonyl or hetarylsulphonyl; and their salts, process and intermediate products for their production, and their use.
Abstract:
Disclosed is a fungicidal mixture containing (1) 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro- [1,2,4]-triazole-3-thion of formula (I) or the salts or adducts thereof, and another fungicidal compound or the salts or adducts thereof, which is dimoxystrobin, in a synergistically active quantity.
Abstract:
Fungicidal mixture (A) comprises prothioconazole (I) and at least one other fungicide (II) selected from trifloxystrobin, picoxystrobin, pyraclostrobin, dimoxystrobin and a strobilurin derivative (N-methyl-2-methoxyimino-2-(2-(3,4-dimethoxyimino-2-pentylideneaminiooxymethyl)phenyl)acetamide). ACTIVITY : Plant antifungal. MECHANISM OF ACTION : None given.
Abstract:
The invention relates to fungicidal mixtures containing 2-[2-(1-chlorcyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione (prothioco-nazoles) of formula (I) or a salt or adduct thereof and another triazole namely metconazole, in a synergistically effective amount.
Abstract:
Wynalazek dotyczy mieszaniny grzybobójczej zawierajacej (1) 2-[2-(1-chlorocyklopropylo)-3-(2-chlorofenylo)-2-hydroksypropylo]-2,4-dihydro[1,2,4]triazolo-3-tion (protiokonazol), albo jego sól lub addukt, i co najmniej jeden inny zwiazek grzybobójczy wybrany z grupy obejmujacej (2) chlorek mepikwatu lub (3) cyjazofamid lub (4) fenoksanil lub (5) zwiazek o wzorze XIII lub (6) tiofanat metylowy lub (7) karbendazym lub (8) metalaksyl lub (9) fludioksonil lub (10) tiabendazol lub (11) kwintocen lub (12) prochloraz lub (13) antrachinon, w synergicznie skutecznej ilosci. Ponadto wynalazek dotyczy sposobu zwalczania szkodliwych grzybów oraz srodka grzybobójczego.