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    • 23. 发明专利
    • Compuestos de enamino(tio)carbonilo bicíclicos
    • ES2420833T3
    • 2013-08-27
    • ES07723361
    • 2007-03-19
    • BAYER CROPSCIENCE AG
    • JESCHKE PETERVELTEN ROBERTSCHENKE THOMASBECK MICHAEL EDMUNDMALSAM OLGARECKMANN UDONAUEN RALFGOERGENS ULRICHPITTA LEONARDOARNOLD CHRISTIANSANWALD ERICH
    • C07D491/04
    • Compuestos de enaminocarbonilo bicíclicos de la fórmula (I)**Fórmula** en la que A representa un resto seleccionado del grupo constituido por 6-cloro-pirid-3-ilo, 6-bromo-pirid-3-ilo, 6-metil-pirid-3-ilo,6-trifluormetil-pirid-3-ilo, 2-metil-pirimidin-5-ilo, 2-cloro-pirimid-5-ilo, 1H-pirazol-4-ilo, que dado el caso está sustituidoen la posición 1 con metilo, etilo, y en la posición 3 con cloro, 1H-pirazol-5-ilo, 3-metil-pirazol-5-ilo, 2-bromo-1,3-tiazol-5-ilo, 2-cloro-1,3-tiazol-5-ilo, isoxazol-5-ilo, que dado el caso está sustituido en la posicón 3 con metilo, etilo,cloro o bromo, 3-metil-1,2,4-oxadiazol-5-ilo, 1-metil-1,2,4-triazol-3-ilo, 1,2,5-tiadiazol-3-ilo, 5-fluoro-6-cloro-pirid-3-ilo,5,6-dicloro-pirid-3-ilo, 5-bromo-6-cloro-pirid-3-ilo, 5-fluoro-6-bromo-pirid-3-ilo, 5-cloro-6-bromo-pirid-3-ilo, 5,6-dibromo-pirid-3-ilo, 5-metil-6-cloro-pirid-3-ilo, 5-metil-6-yodo-pirid-3-ilo y 5-difluorometil-6-cloro-pirid-3-ilo,B representa oxígeno o metileno, E representa CH o C-alquilo, D1-Z-D2 representa una de las agrupaciones químicas siguientes: -CH2-CH2-, -HC>=CH-, -CH2-CH2-CH2-, -CH2-C(>=CH2)-CH2-, -CH2-CO-CH2-, -CH2-CH(OH)-CH2-, -CH2-CF2-CH2-, -CH2-CHF-CH2-, -CH2-CHCl-CH2-, -CH>=CH-CH2-, -CH2-CH2-CH>= -CH2-CH2-CH(OH)-, -CH2-CH(CH3)-CH2-, -CH2-CH2-CH2-CH2-, -CH2-CH>=CH-CH2, -CH2-O-CH2-, -CH2-CH2-O-, -CH2-N(CH3)-CH2-, -CH2-CH2-N(CH3)- o -CH2-S-CH2-, R1 representa hidrógeno, R2 representa hidrógeno, flúor o cloro, y Q representa oxígeno.
    • 26. 发明专利
    • AT554651T
    • 2012-05-15
    • AT05794725
    • 2005-09-21
    • BAYER CROPSCIENCE AG
    • GOERGENS ULRICHJESCHKE PETERLOESEL PETERMALSAM OLGANAUEN RALFTIETJEN KLAUS-GUENTERVELTEN ROBERTPITTA LEONARDOARNOLD CHRISTIANHEMPEL WALTRAUDSANWALD ERICH
    • A01N43/40A01N43/78
    • Use of amino-substituted nitrogen heterocycles (I) for treatment of seeds. Use of amino-substituted nitrogen heterocycles of formula (I) for treatment of seeds. R 1>optionally substituted 5- or 6-membered aromatic heterocycle containing N; X : optionally substituted alkylene or alkylidene; R 2>hydrogen, (cyclo)alkyl, (cyclo)alkenyl or aryl (all optionally substituted) or YR 3>; Y : O, S(O) l, CO or COO; l : 0-2; R 3>hydrogen, (cyclo)alkyl, (cyclo)alkenyl, alkynyl or aryl; A, B and D : optionally substituted C, a heteroatom or a single bond; E : CO or CS; Q : hydrogen, alkyl, alkenyl, alkynyl or aryl (all optionally substituted), nitro, halo or ZR 4>; Z : CO, COO or S(O) m; m : 0-2; R 4>(cyclo)alkyl, (cyclo)alkenyl, alkynyl or aryl (all optionally substituted). An independent claim is also included for a method for controlling animal pests on plants that comprises application of (I) to the soil. [Image] ACTIVITY : Insecticide; Arthropodicide; Arachnicide; Nematocide; Antifouling; Acaricide. A composition containing 3-(N-methyl-N-(2-chloropyridin-5-ylmethyl)amino-2-oxo-1,4-dihydrofuran (Ia), at 4 g/kg, was applied to seeds of cotton, then these planted and 2 weeks later the cotton plants were infested with Aphis gossypii. After 7 days the control of aphids was 100%. (Ia) was also active, from a seed dressing, against A. fabae on beans and Rhopalosiphon padi on barley. MECHANISM OF ACTION : None given.