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    • 72. 发明公开
    • VERWENDUNG VON 5-ALKYL-6-PHENYLALKYL-7-AMINO-AZOLOPYRIMIDINEN, NEUE AZOLOPYRIMIDINE, VERFAHREN ZU IHRER HERSTELLUNG UND SIE ENTHALTENDE MITTEL
    • VERWENDUNG VON 5-烷基-6-苯基烷基-7-氨基偶氮嘧啶,神经氮唑嘧啶,VERFAHREN ZU IHRER HERSTELLUNG UND SIE ENTHALTENDE MITTEL
    • EP1876899A2
    • 2008-01-16
    • EP06754813.1
    • 2006-04-24
    • BASF Aktiengesellschaft
    • DIETZ, JochenGRAMMENOS, WassiliosGROTE, ThomasHÜNGER, UdoLOHMANN, Jan KlaasMÜLLER, BerndRHEINHEIMER, JoachimSCHÄFER, PeterSCHIEWECK, FrankSCHWÖGLER, Anja
    • A01N43/90C07D487/04
    • A01N43/90C07D487/04
    • The invention relates to the use of 5-alkyl-6-phenylalkyl-7-amino-azolopyrimidines of formula (I) for controlling phytopathogenic fungi. The variables in formula I have the following designations: Y represents alkylene, alkenylene or alkinylene, optionally substituted by alkyl groups; R1 represents halogen, cyano, nitro, hydroxy, mercapto, alkyl, halogenalkyl, alkenyl, cycloalkyl, cycloalkenyl, alkoxy, halogenalkoxy, alkenyloxy, alkinyloxy, alkylthio, NRARB, alkylcarbonyl, phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group O, N or S; RA, RB represent hydrogen, alkyl and alkylcarbonyl; n represents 0, 1, 2, 3 or 4; R2 represents alkyl, alkenyl, cycloalkyl, alkoxyalkyl and alkylthioalkyl; R3 represents hydrogen, halogen, cyano, NRARB, hydroxy, mercapto, alkyl, halogenalkyl, cycloalkyl, alkoxy, alkylthio, cycloalkoxy, cycloalkylthio, carboxyl, formyl, alkylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, phenyl, phenoxy, phenylthio, benzyloxy, benzylthio, or alkyl-S(O)m-; m represents 0, 1 or 2; A represents N and C-Ra; and Ra represents hydrogen and alkyl. The carbon atoms in Y, R1, R2, R3 and Ra can be substituted according to the description. The invention also relates to novel 5-alkyl-6-phenylalkyl-7-amino-azolopyrimidines, to methods for producing said compounds, and to agents containing the same.
    • 本发明涉及式(I)的5-烷基-6-苯基烷基-7-氨基 - 唑基嘧啶用于防治植物病原性真菌的用途。 式I中的变量具有以下名称:Y代表任选被烷基取代的亚烷基,亚烯基或亚炔基; R1代表卤素,氰基,硝基,羟基,巯基,烷基,卤代烷基,烯基,环烷基,环烯基,烷氧基,卤代烷氧基,烯氧基,炔氧基,烷硫基,NRARB,烷基羰基,苯基,萘基或五元或六元饱和 含有1至4个选自O,N或S的杂原子的部分不饱和或芳族杂环; RA,RB表示氢,烷基和烷基羰基; n代表0,1,2,3或4; R2代表烷基,烯基,环烷基,烷氧基烷基和烷硫基烷基; R3表示氢,卤素,氰基,NRARB,羟基,巯基,烷基,卤代烷基,环烷基,烷氧基,烷硫基,环烷氧基,环烷硫基,羧基,甲酰基,烷基羰基,烷氧羰基,烯氧羰基,烷氧羰基,苯基,苯氧基,苯硫基, 或烷基-S(O)m-; m表示0,1或2; A代表N和C-Ra; Ra代表氢和烷基。 Y,R1,R2,R3和Ra中的碳原子可以按照说明书进行取代。 本发明还涉及新的5-烷基-6-苯基烷基-7-氨基 - 唑并嘧啶,制备所述化合物的方法,以及含有它们的试剂。
    • 75. 发明公开
    • FUNGIZIDE MISCHUNGEN
    • EP1830650A1
    • 2007-09-12
    • EP05850323.6
    • 2005-12-21
    • BASF Aktiengesellschaft
    • HÜNGER, UdoSTIERL, ReinhardGEWEHR, MarkusNIEDENBRÜCK, Matthias
    • A01N43/80
    • A01N43/80A01N2300/00
    • The invention relates to fungicidal mixtures, containing the following as active components: 1) an isoxazole derivative of formula (I), and 2) at least one active ingredient II selected from the group of azoles, strobilurines, carboxylic acid amides, heterocyclic compounds, carbamates, guanidines, antibiotics, nitrophenyl derivatives, sulphur-containing heterocyclyl compounds, organometal compounds, organophospherous compounds, inorganic active ingredients, cyflufeneamide, cymoxanile, dimethirimol, ethirimol, furalaxyl, metrafenones and spiroxamines in a synergistically active amount thereof.The invention also relates to methods for combatting harmful fungi with mixtures of compound I and active ingredients II and to the use of compound I with active ingredients II in the production of said mixtures and agents containing said mixtures.
    • 本发明涉及杀真菌混合物,其包含以下作为活性组分:1)式(I)的异恶唑衍生物,和2)至少一种选自唑类,嗜球果伞碱,羧酸酰胺,杂环化合物, 氨基甲酸酯,氨基甲酸酯,胍,抗生素,硝基苯衍生物,含硫杂环基化合物,有机金属化合物,有机化合物,无机活性成分,环氟乙烷胺,环氧树脂,二甲基嘧啶,乙嘧酚,呋霜灵, 使用化合物I和活性成分II的混合物来对抗有害真菌的方法,以及使用具有活性成分II的化合物I来制备所述混合物和含有所述混合物的试剂。