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    • 4. 发明授权
    • Quinoline compounds as fungicides or bactericides
    • 喹啉化合物作为杀真菌剂或杀菌剂
    • US5622914A
    • 1997-04-22
    • US529963
    • 1995-09-19
    • Yoshio KurahashiKoichi MoriyaHaruko SawadaHaruhiko SakumaRyo WatanabeAsami Ito
    • Yoshio KurahashiKoichi MoriyaHaruko SawadaHaruhiko SakumaRyo WatanabeAsami Ito
    • A01N43/50A01N43/56C07D401/04C07D521/00C07F7/08A01N43/42C07D215/44
    • C07D231/12A01N43/50A01N43/56C07D233/56C07D249/08C07D401/04C07F7/0812
    • Combatting fungi and bacteria with quinoline derivatives of the formula ##STR1## in which X is a nitrogen atom and Y is a CH-group orY is a nitrogen atom and X is a CH-group,R is hydrogen, halogen, acetyl or alkyl which is optionally substituted by one to three radicals independently selected from the group consisting of alkoxy, phenyl, hydroxy, halogen and cyano, orR is alkenyl which is optionally substituted by one to three radicals independently selected from the group consisting of halogen, cyano, alkoxy, phenyl and hydroxy, orR is alkynyl which is optionally substituted by one to three radicals independently selected from the group consisting of halogen, phenyl, trimethylsilyl, hydroxy, cyano, alkoxy, alkylamino, dialkylamino, alkylcarbonyl, tolyl, alkoxycarbonyl and alkylcarbonyloxy, orR is cycloalkyl which is optionally substituted by one to three radicals independently selected from the group consisting of halogen and cyano,A is hydrogen or halogen andB is halogen or halogenoalkyl,or an acid addition salt or metal salt complex thereof, and processes for their preparation. Most of these compounds are new.
    • 用真菌和细菌与其中X是氮原子并且Y是CH-基团或Y是氮原子并且X是CH-基团的式(I)的喹啉衍生物反应,R是氢,卤素, 乙酰基或烷基,其任选地被一至三个独立地选自烷氧基,苯基,羟基,卤素和氰基的基团取代,或R是任选被一至三个独立地选自卤素 氰基,烷氧基,苯基和羟基,或R是任选被一至三个独立地选自卤素,苯基,三甲基甲硅烷基,羟基,氰基,烷氧基,烷基氨基,二烷基氨基,烷基羰基,甲苯基,烷氧基羰基 和烷基羰基氧基,或R是任选被一至三个独立地选自卤素和氰基的基团取代的环烷基,A是氢或卤素,B是卤素或 卤代烷基或其酸加成盐或金属盐络合物,及其制备方法。 这些化合物大部分是新的。