CAS: 2243-42-7; 2-Phenoxybenzoic Acid

该化合物是一种芳香的碳酸,其特点是芬氧和苯并硫酸功能组,该化合物一般是白色到白外晶状固体,以其在乙醇和乙醇等有机溶剂中的中溶性而闻名,同时在水中不易溶.该化合物的分子结构具有附于苯并氮酸协会正方位的苯氧类(C6H5O-),这助长了其独特的化学特性. 2-苯并氧苯并呋喃酸经常用于各种应用,包括作为有机合成的中间体以及制药和农用化学的生产.此外,它可能展示生物活动,使其对医药化学感兴趣.该化合物在标准条件下的稳定性及其与形成盐基的反作用是显著的特征,可以影响其在化学反应和配制中的行为.

结构式图片

欧盟法规

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1,4-dioxane xanth-9-one tert-butylatepotassium tert-butylate bis(phenyl) carbonate 2-phenoxy-benzoic acid-(2-nitro-anilide) xanth-9-one 2-phenoxy-N-phenylbenzamide methyl 2-phenoxybenzoate

合成工艺路线路线简述

    📜水杨酸苯酯置于potassium Carbonate,Sodium Hydroxide体系中,用 乙醇,水,N,N-二甲基甲酰胺 用作溶剂,化学反应 34.0H,反应生成苯氧苯甲酸
    参考文献:可见光光氧化还原催化从芳基醚到羧酸基团的有效芳基迁移,形成酯.
    标题:可见光光氧化还原催化从芳基醚到羧酸基团的有效芳基迁移,形成酯.
    摘要:通过在环境温度下通过可见光光氧化还原催化的逆向smiles重排,我们开发了从芳基醚到羧酸基团的高效芳基迁移.在转化过程中避免使用过渡金属以及化学计量的氧化剂和碱.受到这种转化的高效率和c-O键断裂的基本重要性的启发,我们开发了一种新颖的方法来联苯醚的c-O裂解形成两个酚类化合物,如一锅,两锅在温和条件下的一步克级反应.芳基迁移表现出广泛的范围,并且可以用于合成诸如醋醋缩丁醛的药物化合物.初期机理研究表明,催化循环是通过还原性淬灭途径发生的.
    Doi:10.1002/anie.201706597

    海关参考信息

    专利信息


    专利号:US-9643915-B2
    优先权日:2013-03-15
    标题:Methods for the synthesis of sphingomyelins and dihydrosphingomyelins
    发明人:ONICIU DANIELA CARMEN; HECKHOFF STEFAN; OSWALD BENOIT; REBMANN PETER; PEER ANDREAS; GONZALEZ MIGUEL; SAUTER PATRIK
    权利人:CERENIS THERAPEUTICS HOLDING SA
    摘要:The present invention includes methods for the synthesis of sphingomyelins and dihydrosphingomyelins. The present invention also includes methods for the synthesis of sphingosines and dihydrosphingosines. The present invention further includes methods for the synthesis of ceramides and dihydroceramides.

    专利号:US-9708354-B2
    优先权日:2013-03-15
    标 题:Methods for the synthesis of sphingomyelins and dihydrosphingomyelins
    发明人:ONICIU DANIELA CARMEN; HECKHOFF STEFAN; OSWALD BENOIT; REBMANN PETER; PEER ANDREAS; GONZALEZ MIGUEL; SAUTER PATRIK
    权利人:CERENIS THERAPEUTICS HOLDING SA
    摘要:The present invention includes methods for the synthesis of sphingomyelins and dihydrosphingomyelins. The present invention also includes methods for the synthesis of sphingosines and dihydrosphingosines. The present invention further includes methods for the synthesis of ceramides and dihydroceramides.

    专利号:WO-2004011474-A1
    优先权日:2002-07-31
    标题:Universal support media for synthesis of oligomeric compounds
    发明人:GUZAEV ANDREI P; MANOHARAN MUTHIAH; RAVIKUMAR VASULINGA T; KUMAR RAJU K
    权利人:ISIS PHARMACEUTICALS INC; GUZAEV ANDREI P; MANOHARAN MUTHIAH; RAVIKUMAR VASULINGA T; KUMAR RAJU K
    摘要:Compounds for the synthesis of oligomeric compounds, particularly oligonucleotide and oligonucleotide mimetics, are provided. In addition, methods for functionalizing a support medium with a first monomeric subunit and methods for the synthesis of oligomeric compounds utilizing the novel compounds bound to support media are provided.

    专利号:US-6653468-B1
    优先权日:2002-07-31
    标 题 :Universal support media for synthesis of oligomeric compounds
    发明人:GUZAEV ANDREI P; MANOHARAN MUTHIAH
    权利人:ISIS PHARMACEUTICALS INC
    摘要:Compounds for the synthesis of oligomeric compounds, particularly oligonucleotides and oligonucleotide mimetics, are provided. In addition, methods for functionalizing a support medium with a first monomeric subunit and methods for the synthesis of oligomeric compounds utilizing the novel compounds bound to support media are provided.

    专利号:US-10919904-B2
    优先权日:2016-08-17
    标 题 :Northern-southern route to synthesis of bacteriochlorins
    发明人:LIU YIZHOU; LINDSEY JONATHAN S; ALLU SRINIVASA RAO; FUJITA HIKARU
    权利人:UNIV NORTH CAROLINA STATE
    摘要:Described herein are chlorins, bacteriochlorins, methods and intermediates for the synthesis of bacteriochlorins, and methods of using such bacteriochlorins for, among other things, diagnostic and therapeutic purposes such as luminescent compounds in flow cytometry, and as active agents in photodynamic therapy (PDT).

    专利号:US-12391691-B2
    优先权日:2018-11-16
    标题:Synthesis of key intermediate of KRAS G12C inhibitor compound
    发明人:PARSONS ANDREW THOMAS; COCHRAN BRIAN MCNEIL; POWAZINIK IV WILLIAM; CAPORINI MARC ANTHONY
    权利人:AMGEN INC
    摘要:The present invention relates to an improved, efficient, scalable process to prepare intermediate compounds, such as compound 5M, having the structure n nuseful for the synthesis of compounds that target KRAS G12C mutations, such as

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    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

    主要参考文献

    [参考文献]: T Schettgen, Et Al. New Gas Chromatographic-Mass Spectrometric Method For The Determination Of Urinary Pyrethroid Metabolites In Environmental Medicine. J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Oct 5;778(1-2):121-30.

    合成参考文献


    摘要:Weibel, J.-M.; Blanc, A.; Pale, P., Science of Synthesis Knowledge Updates, (2018) 1, 101.
    摘要:Sellars, J. D., Science of Synthesis Knowledge Updates, (2014) 1, 408.
    摘要:Kantak, A.; DeBoef, B., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 3, 589.
    摘要:Suna, E.; Shubin, K., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 3, 720.
    摘要:Zhang, M.; Su, W., Science of Synthesis: Catalytic Transformations via CH Activation, (2015) 1, 113.
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