CAS: 16642-92-5; (E)-4-(Trifluoromethyl)Cinnamic Acid

该化合物是能够参与各种化学反应,包括电光替代和迈克尔添加. 丙基酸结构的双层结合有助于其再活动,使其有可能成为聚合的候选物或有机合成的中间体.此外,该化合物可能具有有趣的生物特性,可以用于制药或农业化学应用.其稳定性,溶解性以及与生物系统的互动受到三氟甲基组独特的电子效应的影响,使其在合成化学和医药化学中都受到关注.

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CAS号410086-28-1 7-(trifluoromet... | CAS号53473-36-2 3-(4-三氟甲基苯基)丙酸 | CAS号101488-60-2 3-(4-(三氟甲基)苯基)丙烷-1-胺 | CAS号120681-07-4 3-[4-(trifluoro... | CAS号82989-27-3 3-(4-三氟甲基苯基)丙酸乙酯

合成工艺路线路线简述

    📜3-(4-Trifluoromethylphenyl)-2-Propen-1-Ol置于potassium Phosphate,二氧化碳,Crh6Mo6O24(3-)*3H3N*3H(1+)体系中,用 二甲基亚砜 用作溶剂,80.0 °C,100.0 Kpa 条件下,反应 24.0H,以78%的收率获得4-三氟甲基肉桂酸
    参考文献:使用多金属氧酸盐负载的铬(III)催化剂和co2将醇高效氧化为羧酸
    标题:使用多金属氧酸盐负载的铬(III)催化剂和co2将醇高效氧化为羧酸
    摘要:将醇直接催化氧化为羧酸非常有吸引力,但是尚未建立经济的催化体系.在这里,我们显示纯的无机配体负载的铬化合物(nh 4)3 [crmo 6 O 18(oh)6 ](简化为crmo 6)可用于在存在以下条件下有效地促进此类反应co 2.在几乎所有情况下,各种醇(芳香族和脂肪族)的氧化都可以在温和的条件下完成,相应的羧酸可以高收率实现.铬催化剂1可以重复使用几次,而不会造成活动损失.机理研究和控制反应表明,酸化是通过醛的关键氧化立即进行的.
    Doi:10.1039/d0Gc00388C

    海关参考信息

    专利信息


    专利号:US-6562844-B2
    优先权日:1998-01-23
    标 题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
    发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
    权利人:UPJOHN CO
    摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

    专利号:CN-106220495-A
    优先权日:2016-08-01
    标题 :Method for direct synthesis of unsaturated alkene-containing alpha-acyloxyketone derivatives by α-functionalization reaction of ketones

    专利号:US-7002020-B1
    优先权日:1998-01-23
    标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
    发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V
    权利人:UPJOHN CO
    摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

    专利号:CN-114230519-B
    优先权日:2021-12-06
    标题:A class of pleuromutilin cinnamate compounds with anti-drug-resistant bacteria activity and synthesis method and application thereof

    专利号:JP-H06500076-A
    优先权日:1990-07-18
    标题 :Piperidine compounds, their synthesis and methods of use

    专利号:CN-114605418-B
    优先权日:2022-03-15
    标题 :A class of ibrutinib acrylamide derivatives with anti-tumor activity and its synthesis method and application

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    合成参考文献


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    摘要:Vashchenko, B. V.; Grygorenko, O. O., Science of Synthesis Knowledge Updates, (2021) 3, 399.
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    摘要:Parmeggiani, F.; Galman, J. L.; Montgomery, S. L.; Turner, N. J., Science of Synthesis, (2019) , 408.
    摘要:Fujihara, T., Science of Synthesis: Special Topics, (2022) 1, 374.
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