\u63a7\u5236\u7ec6\u83cc\u548c\u6c61\u57a2\u751f\u7269\u7684\u65b9\u6cd5\uff0c\u6240\u8ff0\u65b9\u6cd5\u5305\u62ec\u5411\u6240\u8ff0\u7ec6\u83cc\u6216\u6c61\u57a2\u751f\u7269\u6216\u5411\u5176\u6ecb\u751f\u5730\u65bd\u7528\u6709\u6548\u6297\u83cc\u6216\u9632\u6c61\u91cf\u7684\u5982\u4e0b\u901a\u5f0f\u5316\u5408\u7269 \uff0a\uff0a\uff0a \uff08\u2160\uff09 \u5f0f\u4e2d\uff4e\u662f\uff10\u3001\uff11\u6216\uff12\uff1b\uff32\u2191\uff3b\uff11\uff3d\u662f\u6c22\u3001\uff23\u2193\uff3b\uff11\uff0d\uff14\uff3d\u70f7\u57fa\u6216\u82c4\u57fa\uff1b\u4e14\uff32\u4ee3\u8868\uff08\uff41\uff09\u82ef\u57fa\uff1b\u88ab\uff11\uff5e\uff13\u4e2a\u72ec\u7acb\u9009\u81ea\u4e0b\u5217\u7684\u53d6\u4ee3\u57fa\u56e2\u53d6\u4ee3\u7684\u82ef\u57fa\uff1b\u7f9f\u57fa\uff0c\u5364\u539f\u5b50\uff0c\uff23\u2193\uff3b\uff11\uff0d\uff11\uff12\uff3d\u70f7\u57fa\u3001\uff23\u2193\uff3b\uff15\uff0d\uff16\uff3d\u73af\u70f7\u57fa\u3001\u4e09\u5364\u7532\u57fa\uff0c\u82ef\u57fa\uff0c\uff23\u2193\uff3b\uff11\uff0d\uff15\uff3d\u70f7\u6c27\u57fa\uff0c\uff23\u2193\uff3b\uff11\uff0d\uff15\uff3d\u70f7\u786b\u57fa\uff0c\u56db\u6c22\u5421\u5583\u6c27\u57fa\uff0c\u82ef\u6c27\u57fa\uff0c\uff23\u2193\uff3b\uff11\uff0d\uff14\uff3d\u70f7\u7fb0\u57fa\uff0c\u82ef\u7532\u9170\uff0c\uff23\u2193\uff3b\uff11\uff0d\uff14\uff3d\u70f7\u57fa\u4e9a\u78fa\u9170\uff0c\uff23\u2193\uff3b\uff11\uff0d\uff14\uff3d\u70f7\u57fa\u78fa\u9170\uff0c\u7fa7\u57fa\u6216\u5176\u78b1\u91d1\u5c5e\u76d0\uff0c\uff23\u2193\uff3b\uff11\uff0d 4 alkoxycarbonyl, C: 1 - 4 alkyl amino carbonyl amino carbonyl amino toluene, benzene, carbonyl, carbonyl morpholino, amino, nitro, cyano, two dioxolane based or C: 1 - 4 alkoxy imino methyl naphthyl;; pyridine; thiophene, as well n is not 2 or 1; furan group; ~ 3 independently selected from the group consisting of substituent groups following substituted thiophene or furan group; C: 1: 4: 1: C alkyl, alkoxy 4, C: 1 - 4 alkylthio, a halogen atom, a cyano group formyl, acetyl, benzoyl, nitro, C: 1 - 4 alkoxycarbonyl, phenyl, phenyl amino carbonyl and C: 1 - 4 alkoxy iminomethyl; or R on behalf of the general formula group, (b) * * * type X is oxygen or sulfur: Y is nitrogen, CH or C (C Case 1 - 4 alkoxy): and R is hydrogen or C down 1 - 4 alkyl.
【技术实现步骤摘要】
本专利技术涉及一种用3-芳基-5,6-二氢-1,4,2-噁噻嗪及其氧化物控制细菌和污垢生物的方法,一种保护非木非生物材料的方法,和工业抗菌防污组合物,暴露于潮湿环境或水环境的物体表面容易附生微生物,偶尔也附生其它更高级的生命形式,如软体动物和甲壳动物。当这些生物定居或附着到所述表面上时,暴露物体的价值便随之下降。该物体的外表面,但可能也包括其内表面,可能会恶化,表面状况改变(例如,从光滑、清洁和流线型变成粗糙、污垢和湍流型),物体重量因生物及其遗留物的沉积而增加,该物体周围也可能变得阻塞或拖累。有关物体和系统的功能下降,水环境的质量恶化。类似的问题侵袭着工业上使用的组合物如涂料、润滑剂等。所有这些现象统称污垢。本方法的噁噻嗪及其氧化物在US-4,569,690中是作为除草剂、植物杀真菌剂、植物干燥剂和脱叶剂公开的。本专利技术提供一种控制细菌和污垢生物的方法,所述方法包括向所述细菌或污垢生物或向其所在部位施用一有效抗菌或防污量的如下通式化合物, 式中n是0、1或2;R1是氢、C1-4烷基或苄基;且R代表(a)苯基;被1~3个独立选自下列的取代基团取代的苯基羟基 ...
【技术保护点】
【技术特征摘要】
【专利技术属性】
技术研发人员:J·F·E·范吉斯特尔,
申请(专利权)人:詹森药业有限公司,
类型:发明
国别省市:
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