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    • 105. 发明公开
    • 2-SUBSTITUIERTE PYRIMIDINE
    • 2-取代苯基嘧啶
    • EP1613605A1
    • 2006-01-11
    • EP04724259.9
    • 2004-03-30
    • BASF Aktiengesellschaft
    • TORMO I BLASCO, JordiBLETTNER, CarstenMÜLLER, BerndGEWEHR, MarkusGRAMMENOS, WassiliosGROTE, ThomasGYPSER, AndreasRHEINHEIMER, JoachimSCHÄFER, PeterSCHIEWECK, FrankSCHWÖGLER, AnjaWAGNER, OliverSCHERER, MariaSTRATHMANN, SiegfriedSCHÖFL, UlrichSTIERL, Reinhard
    • C07D239/28C07D239/34C07D239/42C07D239/46C07D239/52A01N43/54
    • A01N43/54C07D239/28C07D239/30
    • The invention relates to 2-substituted pyrimidines of formula (I), in which the value n and the substituents L, Ra, Rb, Rc, Rz, Ru, Rv, A?, A and A are defined as cited in the description and: R1 represents C3-C10 alkyl, C3-C10 alkenyl, C3-C10 alkynyl, C3-C12 cycloalkyl, C3-C10 cycloalkenyl, or a five to ten-membered, saturated, partially unsaturated or aromatic heterocycle, bonded by carbon and containing one to four heteroatoms from the group O, N or S; R2 represents halogen, cyano, C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, C1-C4 alkoxy, C3-C4 alkenyloxy or C3-C4 alkynyloxy, whereby the alkyl, alkenyl and alkynyl groups of R2 can be substituted by halogen, cyano, nitro, C1-C2 alkoxy or C1-C4 alkoxycarbonyl; and R3 represents cyano, CO2Ra, C(=O)NRzRb, C(=O)-N-ORb, C(=S)-NRaRb, C(=NORa)NRzRb, C(=NRa)NRzRb, C(=O)NRa-NRzRb, C(=N-NRzRc)NRaRb, C(=O)Ra, C(=NORb)Ra, C(=N-NRzRb)Ra, CRaRb-ORz, CRaRb-NRzRc, ON(=CRaRb), O-C(=0)Ra, NRaRb', NRa(C(=O)Rb), NRa(C(=O)ORb), NRa(C(=0)-NRzRb), NRa(C(=NRc)Rb), N-Ra(N=CRcRb), NRa-NRzRb, NRz-ORa, NRa(C(=NRc)-NRzRb), NRa(C(=NORc)Rb). The invention also relates to a method for producing said compounds, to agents containing the latter and to their use as pesticides.
    • 本发明涉及式(I)的2-取代的嘧啶,其中值n和取代基L,Ra,Rb,Rc,Rz,Ru,Rv,A',A和A如说明书中所引用的那样定义和 :R1表示碳,并且含有一个碳原子的C3-C10烷基,C3-C10烯基,C3-C10炔基,C3-C12环烷基,C3-C10环烯基或五至十元饱和,部分不饱和或芳族杂环 至O,N或S组中的四个杂原子; R2表示卤素,氰基,C1-C4烷基,C2-C4链烯基,C2-C4炔基,C1-C4烷氧基,C3-C4链烯氧基或C3- 卤素,氰基,硝基,C 1 -C 2烷氧基或C 1 -C 4烷氧基羰基; (= O)-N-ORb,C(= S)-NRaRb,C(= NORa)NRzRb,C(= NRa)NRzRb,C(= O)NRzRb, (= CRaRb)NRa-NRzRb,C(= N-NRzRc)NRaRb,C(= O)R a,C(= NORb)Ra,C(= N-NRzRb)Ra,CRaRb-ORz,CRaRb- ,OC(= O)Ra,NRaRb',NRa(C(= O)Rb),NRa(C(= O)ORb),NRa(C(= O)-NRzRb),NRa(C(= NRc)Rb ),N-Ra(N = CRcRb),NRa-NRzRb,NRz-Ora,NRa(C(= NRc)-NRzRb),NRa(C(= NORc)Rb)。 本发明还涉及生产所述化合物的方法,含有所述化合物的试剂以及它们作为杀虫剂的用途。
    • 106. 发明公开
    • TRIFLUORMETHYL-THIOPHENCARBONSÄUREANILIDE UND IHRE VERWENDUNG ALS FUNGIZIDE
    • 三氟甲基THIOPHENCARBONSÄUREANILIDE及其作为杀菌剂
    • EP1608637A1
    • 2005-12-28
    • EP04722169.2
    • 2004-03-20
    • BASF Aktiengesellschaft
    • GEWEHR, MarkusMÜLLER, BerndGROTE, ThomasGRAMMENOS, WassiliosGYPSER, AndreasTORMO I BLASCO, JordiSCHWÖGLER, AnjaRHEINHEIMER, JoachimBLETTNER, CarstenSCHIEWECK, FrankRACK, MichaelSCHÖFL, UlrichSTRATHMANN, SiegfriedSTIERL, ReinhardRETHER, Jan
    • C07D333/12
    • C07D333/38
    • The invention relates to trifluoromethyl-thiophene carboxylic acid anilides of general formulas I, II, and III, wherein the substituents have the following meaning: R1, R4 independently represent C1-C4 alkyl, C3-C6 cycloalkyl, C2-C4 alkenyl, C2-C4 alkinyl, C1-C4 alkoxy, said groups being optionally substituted by halogen, H, halogen, nitro, CN; R2 represents H, OH, C1-C4 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, said groups being optionally substituted by halogen; R3 represents C1-C12 alkyl, C3-C12 cycloalkyl, C2-C12 alkenyl, C5-C12 cycloalkenyl, C2-C12 alkinyl, C3-C12 cycloalkyl-C1-C4 alkyl, said groups being optionally substituted by R7; phenyl, phenyl-C1-C6 alkyl, phenyl-C2-C6 alkenyl, phenyl-C2-C6 alkinyl, phenyloxy-C1-C6 alkyl, phenyloxy-C2-C6 alkenyl, phenyloxy-C2-C6 alkinyl, the alkyl portion, alkenyl portion, and alkinyl portion being optionally substituted by R7 and the phenyl ring being optionally substituted by R5; -C(R8)=NOR6; X represents O, S, or a direct bond; R5 represents H, C1-C4 alkyl, C3-C6 cycloalkyl, C1-C4 alkoxy, C2-C4 alkenyl, C2-C4 alkinyl, said groups being optionally substituted by halogen, halogen, nitro, CN, phenyl which can be substituted by R1, phenoxy that can be substituted by R1, C1-C6 alkyl-phenyl, the alkyl portion being optionally substituted by halogen and the phenyl ring being optionally substituted by R1; R6 represents C1-C4 alkyl, C3-C6 cycloalkyl, C2-C4 alkenyl, C2-C4 alkinyl, said groups being optionally substituted by halogen, phenyl which can be substituted by R1; R7 represents C1-C4 alkyl, C1-C8 alkoxy, C2-C8 alkenyloxy, C2-C8 alkinyloxy, C1-C4 alkoxy-C1-C8 alkoxy, said groups being optionally substituted by halogen, halogen; R8 represents H, R7, or C1-C12 alkyl, C3-C12 cycloalkyl, C2-C12 alkenyl, C5-C12 cycloalkenyl, C3-C12 cycloalkyl-C1-C4 alkyl, said groups being optionally substituted by halogen; phenyl which can be substituted by R5; n represents 0 to 4; and m represents 0, 1. Also disclosed is the use of the inventive trifluoromethyl-thiophene carboxylic acid anilides as fungicides and agents containing said trifluoromethyl-thiophene carboxylic acid anilides.