FUNGICIDAL COMPOSITIONS
    83.
    发明专利

    公开(公告)号:CA2806011A1

    公开(公告)日:2012-02-09

    申请号:CA2806011

    申请日:2011-08-02

    Applicant: BASF SE

    Abstract: The present invention relates to compositions of fungicidally active compounds com- prising at least one active compound I selected from 3-difluoromethyl-1-methyl-1H- pyrazole-4-carboxylic acid (3',4',5'-trifluoro-biphenyl-2-yl)-amide (fluxapyroxade), bixafen, fluopyram, isopyrazam, sedaxane, penflufen andpenthiopyrad and at least one further active component II as defined below. The invention furthermore relates to a method for controlling harmful fungi, wherein the fungi, their habitat or the plant propagation material, the soil, the plants or the materials to be protected against fungal attack are treated with an effective amount of at least one active compound I in combination with at least one active component II or with an effective amount of a composition according to the invention, to a method for protection of plant propagation material, comprising contacting the plant propagation material with an effective amount of at least one active compound I in combination with at least one active component II or with an effective amount of a composition according to the invention, to a method for protecting plants after germination from the attack of foliar phytopathogenic fungi, which comprises treating the plant propagation material from which the plants are to grow with an effective amount of at least one active compound I in combination with at least one active component II or with an effective amount of a composition according to the invention, to the use of the composition according to the invention for controlling harmful fungi, and to plant propagation material comprising the composition.

    87.
    发明专利
    未知

    公开(公告)号:BRPI0711546A2

    公开(公告)日:2011-11-08

    申请号:BRPI0711546

    申请日:2007-04-11

    Applicant: BASF SE

    Abstract: The invention relates to 3-(pyridin-2-yl)-[1,2,4]-triazines of formula (I) and their use in the control of parasitic fungi and to herbicides that contain said compounds as an effective ingredient thereof. In formula (I), R1, R2 independently represent OH, halogen, NO2, NH2, C1-C8 alkyl, C1-C8 alkoxy, C1-C8 halogenalkyl, C1-C8 halogenalkoxy, C1-C8 alkylamino or di(C1-C8 alkyl)amino, or they form, together with the C atoms to which they are bound, a saturated five-, six- or seven-membered carbocycle or heterocycle, which, in addition to the carbon ring members, has one or two heteroatoms selected from oxygen or sulfur as the ring members, the carbocycle and the heterocycle being unsubstituted or having 1, 2, 3 or 4 C1-C4 alkyl groups as the substituents; R3 represents hydrogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, or halogen; R4 represents hydrogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy or halogen; R5 represents C1-C8 alkyl, C1-C8 halogenalkyl, C1-C8 alkoxy, C1-C8 halogenalkoxy, C3-C8 cycloalkyl, C3-C8 cycloalkyloxy, five- or six-membered heteroaryl, phenyl, phenoxy, benzyl, benzyloxy, five- or six-membered heteroarylmethyl or five- or six-membered heteroaryloxy, said cyclic groups being unsubstituted or having 1, 2, 3, 4 or 5 groups Ra.

    METHOD FOR PRODUCING DIFLUOROMETHYL-SUBSTITUTED PYRAZOLE COMPOUNDS

    公开(公告)号:ZA201000204B

    公开(公告)日:2011-10-26

    申请号:ZA201000204

    申请日:2010-01-12

    Applicant: BASF SE

    Abstract: The present invention relates to a process for preparing 3-difluoromethyl-Substituted pyrazole compounds of the formula (I) in which R1 is H, halogen, nitro, C1-C8-alkyl, C1-C8-haloalkyl, C3-C8-cycloalkyl, phenyl, naphthyl, hetaryl, cyano, —C(═O)—OR1a, —C(═O)—NR1bR1c, —C(═O)—SR1d or —C(═S)—SR1e; R2 is H, C1-C4-alkyl, benzyl or phenyl; R3 is H, halogen, C1-C8-alkoxy, C1-C8-haloalkoxy, C3-C8-cycloalkoxy, C2-C8-alkenyloxy, C1-C8-alkylthio, C1-C8-haloalkylthio, C3-C8-cyclo-alkylthio or C2-C8-alkenylthio; compounds of the formula (II.a) or (II.b), in which R1 and R3 each have one of the definitions given above; R4 is halogen, —OR4a, —SR4a, —O—SO2—R4a or an —NR4bR4c group; R5 and R6 are each C1-C8-alkyl, C1-C8-haloalkyl, C3-C8-cycloalkyl, benzyl or phenyl, or, together with the nitrogen atom to which they are bonded, are a 3- to 8-membered heterocycle; Lewis acid adducts of compounds of the formula (II.b); the use of compounds of the formula (II.a) or (II.b) and of the Lewis acid adducts for preparing compounds of the formula (I) or (VI); and to a process for converting such compounds to the corresponding 3-difluoro-pyrazol-4-ylcarboxylic acids.

    89.
    发明专利
    未知

    公开(公告)号:BRPI0710774A2

    公开(公告)日:2011-06-21

    申请号:BRPI0710774

    申请日:2007-05-02

    Applicant: BASF SE

    Abstract: The invention relates to the use of arylcarbonic acid biphenylamides of formula (I) wherein X is halogen or methyl; n is zero, 1 or 2; Y is cyano, nitro, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-halo-alkoxy, C1-C4-alkylthio, C1-C4-haloalkylthio, C1-C4-alkoxy-iminomethyl or allyloxy-iminomethyl; m is zero to 5; Ar is an aryl radical of the formula IIa, IIb or IIc wherein R1 is hydrogen, halogen, C1-C4-alkyl or C1-C4-haloalkyl, R2 is C1-C4-alkyl, R3 is hydrogen, halogen or methyl, R4 is hydrogen, halogen or C1-C4-alkyl, R5 is C1-C4-alkyl or C1-C4-haloalkyl, Z is CH or N and R6 is halogen, C1-C4-alkyl or C1-C4-haloalkyl, for seed treatment for protecting plants after germination from the attack of foliar phytopathogenic fungi and corresponding methods of seed treatment for protecting plants after germination from the attack of foliar phytopathogenic fungi. The invention also relates to seed treatment formulations comprising the arylcarboxylic acid biphenylamides of formula (I), and to seeds treated therewith.

    3-(PIRIDIN-2-IL)-[1,2,4]-TRIAZINAS COMO FUNGICIDAS.

    公开(公告)号:ES2358615T3

    公开(公告)日:2011-05-12

    申请号:ES07727983

    申请日:2007-04-11

    Applicant: BASF SE

    Abstract: Compuestos de 3-(piridin-2-il)-[1,2,4]-triazina de la fórmula general I en la que: R 1 , R 2 representan independientemente uno de otro OH, halógeno, NO2, NH2, alquilo de C1-C8, alcoxi de C1-C8, haloalquilo de C1-C8, haloalcoxi de C1-C8, alquilamino de C1-C8 o di(alquil de C1-C8)amina, o conjuntamente con los átomos de C, al que están enlazados, pueden formar un carbociclo o heterociclo saturado de 5, 6 ó 7 miembros el cual tiene, además de los miembros de carbono del anillo uno o dos heteroátomos seleccionados entre oxígeno y azufre como miembros de anillo, en cuyo caso el carbociclo y el heterociclo están sin sustituir o tienen 1, 2, 3 ó 4 grupos alquilo de C1-C4 como sustituyentes; R 3 representa hidrógeno, alquilo de C1-C4, alcoxi de C1-C4, haloalquilo de C1-C4, haloalcoxi de C1-C4, cicloalquilo de C3-C6, cicloalquilmetilo de C3-C6 o halógeno; R 4 representa hidrógeno, alquilo de C1-C4, alcoxi de C1-C4, haloalquilo de C1-C4, haloalcoxi de C1-C4 o halógeno; R 5 representa alquilo de C1-C8, haloalquilo de C1-C8, alcoxi de C1-C8, haloalcoxi de C1-C8, cicloalquilo de C3-C8, cicloalquil(de C3-C8)oxi, heteroarilo de de 5 ó 6 miembros, fenilo, fenoxi, bencilo, benciloxi, heteroarilmetilo de 5 ó 6 miembros o heteroariloxi de 5 ó 6 miembros, en cuyo caso Los residuos cíclicos nombrados previamente están sin sustituir o pueden tener 1, 2, 3, 4 ó 5 residuos R a , en cuyo caso R a se selecciona entre OH, SH, halógeno, NO2, NH2, CN, COOH, alquilo de C1-C8, alcoxi de C1-C8, haloalquilo de C1-C8, haloalcoxi de C1-C8, alquilamino de C1-C8, di(alquil de C1-C8)amina, alquil(de C1-C8)tio, haloalquil(de C1­ C8)tio, alquil(de C1-C8)sulfinilo, haloalquil(de C1-C8)sulfinilo, alquil(de C1-C8)sulfonilo, haloalquil(de C1-C8)sulfonilo, cicloalquilo de C3-C8, fenilo, fenoxi y residuos de la fórmula C(=Z)R aa , donde Z representa O, S, N(alquilo de C1-C8), N(alcoxi de C1-C8), N(alqueniloxi de C3-C8) o N(alquiniloxi de C3-C8) y R aa significa hidrógeno, alquilo de C1-C8, alcoxi de C1-C8 NH2, alquilamino de C1-C8 o di(alquil de C1-C8)amino, o dos residuos R a enlazados con átomos de C adyacentes también pueden formar conjuntamente con los átomos de C, con los que están enlazados, un carbociclo saturado de 5, 6 ó 7 miembros, un anillo de benceno o un heterociclo de 5, 6 ó 7 miembros, el cual tiene como miembros de anillo, además de los carbonos miembros de anillo, uno o dos heteroátomos seleccionados entre oxígeno y azufre, en cuyo caso el carbociclo y el heterociclo están sin sustituir o tienen 1, 2, 3 ó 4 grupos alquilo de C1-C4 como sustituyentes; y las sales útiles en la agricultura de los compuestos de la fórmula I, a excepción de: 2,6-Bis-(5,6-dimetil-1,2,4-triazin-3-il)piridina; 2,6-Bis-(5,6-dietil-1,2,4-triazin-3-il)piridina; 2,6-Bis-(5,6-dipropil-1,2,4-triazin-3-il)piridina; 2,6-Bis-(5,6-diisopropil-1,2,4-triazin-3-il)piridina; 35 2,6-Bis-(5,6-dibutil-1,2,4-triazin-3-il)piridina; 2,6-Bis-(5,6-diisobutil-1,2,4-triazin-3-il)piridina; 2,6-Bis-(5,6-dipentil-1,2,4-triazin-3-il)piridina; 2,6-Bis-(5,6-dihexil-1,2,4-triazin-3-il)piridina; 2,6-Bis-(5,6-diheptil-1,2,4-triazin-3-il)piridina; 3-[6-(2,2'-bipiridil)]-5,6-dimetil-1,2,4-triazina; 3-[6-(2,2'-bipiridil)]-5,6-dietil-1,2,4-triazina; 3-[6-(2,2'-bipiridil)]-5,6-dipropil-1,2,4-triazina; 3-[6-(2,2'-bipiridil)]-5,6-dibutil-1,2,4-triazina; 5,6-Dietil-3-[6-(2-piridil)-4-metoxipiridin-2-il]-1,2,4-triazina; 3-(6-Metilpiridin-2-il)-5,6-dimetil-1,2,4-triazina; 3-(6-Metilpiridin-2-il)-5,6-dietil-1,2,4-triazina; 2,6-Bis-(5,6-dimetoxi-1,2,4-triazin-3-il)piridina; y 2,6-Bis-(5,6-dietoxi-1,2,4-triazin-3-il)piridina.

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