CAS: 220996-80-5; 4-Bromo-2-(Trifluoromethoxy)Benzaldehyde

该化合物是苯环上一种多用途芳烃藻类,以溴和三氟甲基苯氧替代物为特征,该化合物在有机合成中特别宝贵,作为制备药品,农用化学品和特殊材料的关键中间体;使用电离式三氟氧基组的存在可增强再活性,便利选择性转化,而溴代苯则通过交叉反应为进一步功能化提供一个处理器.其高纯度和稳定性使其适合要求合成应用.研究人员支持该化合物,因为它能够引入含三氟苯氧基质,由于其代谢稳定性和脂性增强特性,在药物发现中日益重要.

结构式图片

欧盟法规

C&L通报

上下游产品

CAS号947583-96-2 4-溴-2-(三氟甲氧基)苯甲胺

合成工艺路线路线简述

    📜4-溴-2-(三氟甲氧基)碘苯置于正丁基锂,水体系中,用 四氢呋喃,正己烷,Hexanes 用作溶剂,化学反应 6.0H,以78.6%的收率获得4-溴-2-(三氟甲氧基)苯甲醛
    参考文献:Wo2007/98352
    标题:Wo2007/98352

    海关参考信息

    专利信息


    专利号:WO-2010096722-A1
    优先权日:2009-02-20
    标 题 :3-oxo-2, 3-dihydro- [1,2, 4] triazolo [4, 3-a]pyridines as soluble epoxide hydrolase (seh) inhibitors
    发明人:FENG JUN; KEUNG WALTER; NOTZ WOLFGANG REINHARD LUDWIG
    权利人:TAKEDA PHARMACEUTICAL; FENG JUN; KEUNG WALTER; NOTZ WOLFGANG REINHARD LUDWIG
    摘要:Claimed are intermediates in the synthesis of N-Arylmethyl-3-Oxo-2,3-dihydro- [1,2,4]triazolo[4,3-a]pyridine-6-carboxamides as well as a process (A) to arrive at 3-Oxo-2, 3-dihydro-[1,2,4]triazolo[4,3-a]pyridine-6-carboxylic acid. The triazolo[4,3-a]pyridine-6-carboxamides of formula (I) are used as soluble epoxide hydrolase inhibitors (sEH) having therapeutic effect in pathologic conditions such as hypertension, stroke, inflammatory processes, diabetes and a variety of cardiovascular diseases.

    专利号:US-6090805-A
    优先权日:1997-06-18
    标 题 :Tocolytic oxytocin receptor antagonists
    发明人:WILLIAMS PETER D; SPARKS MICHELLE A; BELL IAN; PERLOW DEBRA S; STAUFFER KENNETH; FREIDINGER ROGER M
    权利人:MERCK & CO INC
    摘要:This invention relates to certain novel benzoxazinone compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor in mammals, especially humans. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery.

    专利号:US-5968938-A
    优先权日:1997-06-18
    标 题 :Piperazine oxytocin receptor antagonists
    发明人:WILLIAMS PETER D; SPARKS MICHELLE A; BELL IAN; GUARE JR JAMES P; FREIDINGER ROGER M
    权利人:MERCK & CO INC
    摘要:This invention relates to certain novel piperazine compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor in mammals, especially humans. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知