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    • 5. 发明授权
    • Fungicidal mixtures
    • US06346535B1
    • 2002-02-12
    • US09240412
    • 1999-01-29
    • Henry Van Tuyl CotterGunther ReichertEwald SieverdingPetrus Martinus Franciscus Emanuel Jegerings
    • Henry Van Tuyl CotterGunther ReichertEwald SieverdingPetrus Martinus Franciscus Emanuel Jegerings
    • A01N4354
    • A01N35/04A01N59/20A01N59/02A01N55/00A01N47/44A01N47/38A01N47/14A01N47/04A01N43/90A01N43/84A01N43/82A01N43/76A01N43/653A01N43/60A01N43/56A01N43/54A01N43/40A01N43/42A01N43/36A01N43/32A01N43/30A01N37/50A01N37/46A01N37/38A01N37/34A01N37/06A01N2300/00
    • The invention relates to a novel fungicidal composition comprising synergistically effective amounts of at least one benzophenone of formula I wherein R1 represents a halogen atom, an optionally substituted alkyl, alkanoyloxy or alkoxy group; or a hydroxy group, R2 represents a halogen atom or an optionally substituted alkyl group, R3 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group or a nitro group; m is 0 or an integer of 1 to 3; R4 represents a halogen atom, a cyano, carboxy, hydroxy or nitro group or an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulphinyl, alkylsulphonyl or amino group; R5 represents an optionally substituted alkyl group; R6 represents a halogen atom or a nitro group, an optionally substituted alkyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, cycloalkyl, cycloalkyloxy, aryloxy group; R7 independently represents a halogen atom, an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkoxy group; n is 0 or 1; and at least one fungicidally active ingredient selected from the groups consisting of (A), (B), (C), (D) and (E) wherein: (A) is an ergosterol biosynthesis inhibitor; (B) is a strobilurine derivative, (C) is a melanin biosynthesis inhibitor; (D) is a compound selected from the group consisting of acibenzolar, benomyl, captan, carboxin, chlorothalonil, copper, cyprodinil, dinocap, dithianon, dimethomorph, dodine, ethirimol, famoxadone, fenpiclonil, fluazinam, mancozeb, metalaxyl, pyrifenox, sulfur, vinclozolin and (E) is an azolopyrimidine of formula II  iwherein R8 and R9 each independently represent hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl, aryl, heteroaryl, cycloalkyl, bicycloalkyl or heterocyclyl group, or R8 and R9 together with the interjacent nitrogen atom represent an optionally substituted heterocyclic ring, R10 represents hydrogen or an alkyl or aryl group, R11 represents a hydrogen or halogen atom or an alkyl or alkoxy group, L independently represents a halogen atom or an optionally substituted alkyl or alkoxy group, p is 0 or an integer from 1 to 5; and A represents N or CR2, wherein R12 has the meaning given for R10; together with a fungicidally acceptable carrier and/or surface active agent, and to a method of controlling the growth of phytopathogenic fungi which comprises applying synergistically effective amounts of the composition to the locus.