CAS: 21211-22-3; 3-Chlorobenzo[b]Thiophene-2-Carboxylic Acid

该化合物是一种有机化合物,其独特结构包括一个氯化苯并苯乙酰环和一个碳酸功能组;苯并苯并[b]thiophene 3位置的氯原子的存在增强了其反应力并影响其物理特性,如溶性点和沸点;该化合物一般在有机溶剂中表现出中等溶性,水溶性有限;由于硫苯环的疏水性,该化合物具有独特的结构特征. 碳箱酸组有助于其酸性,使其能够参与各种化学反应,包括酯化和恐吓.此外,3-Crlorobenzo[b]thiophene-2-carboxylicine酸可能展示生物活动,使其对药物研究感兴趣.其结构特征还表明材料科学和有机合成可能应用.正如许多化学物质一样,处理应谨慎,并遵循其潜在再活动和毒性的安全议定书.

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ECHA物质C&L通报

上下游产品

3-chlorobenzo[b]thiophen-2-carbonyl chloride 3-chlorobenzo[b]thiophene-2-carboxylic acid methyl ester Cinnamic acid 3-Phenylpropionic acid Benzo[b]thiophene 3-chlorobenzo[b]thiophen-2-carbonyl chloride N-(4-chlorophenyl)-2-[((3-chlorobenzo[b]thien-2-yl)carbonyl)amino]-5-methylbenzamide 3-chloro-N-[2-[[(4-fluorophenyl)amino]carbonyl]-4-methylphenyl]benzo[b]thiophene-2-carboxamide

合成工艺路线路线简述

    📜3-苯基丙酸置于吡啶,氯化亚砜体系中,用35%的收率获得3-氯苯并(B)噻吩-2-羧酸
    参考文献:Agents And Methods For Treating Ischemic And Other Diseases
    标题:Agents And Methods For Treating Ischemic And Other Diseases
    摘要:该发明涉及调节trpm7蛋白活性的化合物,以及将其用于治疗或预防缺血,癌症,疼痛或青光眼的用途.

    海关参考信息

    专利信息


    专利号:US-6531470-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; 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: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: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:US-8242142-B2
    优先权日:2008-08-19
    标题:Cyclohexylamines, phenylamines and uses thereof
    发明人:LIN SHUO; YANG ZHEN
    权利人:LIN SHUO; YANG ZHEN; UNIV CALIFORNIA; UNIV PEKING SHENZHEN GRAD SCHO
    摘要:Compounds having the formula I, their methods of synthesis, and pharmaceutically acceptable salts of certain of them are provided in which the variables have the definitions described herein. n n n n n n n n n n Compositions including the compounds having the formula I-A in which the variables have the definitions described herein, and methods of using the compositions for the treatment of certain diseases mediated by the up-regulation of Smo are also disclosed.

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1021/jm301448p
    摘要:Friberg A, Vigil D, Zhao B, Daniels RN, Burke JP, Garcia-Barrantes PM, Camper D, Chauder BA, Lee T, Olejniczak ET, Fesik SW. Discovery of potent myeloid cell leukemia 1 (Mcl-1) inhibitors using fragment-based methods and structure-based design. J Med Chem. 2013 Jan 10;56(1):15–30.
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