CAS: 73035-16-2; 3-Acetylbenzenesulfonyl Chloride

该化合物是一种多用途的全氟辛烷磺酸试剂,广泛用于有机合成和制药中间体,其主要优点包括作为电极的高反应性,能够对氨,酒精和其他核素进行高效的磺化.处于元体位置的乙酰集团增强了其稳定性,同时允许进一步实现功能化.该化合物对于编制全氟辛烷磺酸,全氟辛烷磺酸酯和其他具有药用化学和物质科学用途的衍生物特别宝贵.该化合物在普通有机溶剂中表现出良好的溶解性,便于对合成工作流程进行直接处理.该产品的明确界定的结构确保了多步合成的一贯性,使其成为研究和工业应用的可靠选择.

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CAS号111711-76-3 1-(3-acetylphen...

合成工艺路线路线简述

    📜间氨基苯乙酮置于盐酸,Sodium Nitrite,二氧化硫,溶剂黄146,Copper(L) Chloride体系中,用 水 作为反应溶剂,化学反应 1.83H,反应生成 3-乙酰基苯磺酰氯
    参考文献: Lox Enzyme Inhibiting Methods And Compositions[fr] Procédés Et Compositions D'Inhibition De L'Enzyme Lox
    标题: Lox Enzyme Inhibiting Methods And Compositions[fr] Procédés Et Compositions D'Inhibition De L'Enzyme Lox
    摘要:这项发明涉及化合物,药物组合物及其用于治疗纤维化疾病,增殖性疾病,心血管疾病,急性和慢性炎症性疾病,原发性和转移性癌症,肺部疾病,眼部疾病或神经系统和神经精神疾病的用途.发明的一个特定方面涉及赖氨酸氧化酶酶家族的抑制剂及其作为治疗纤维化疾病的药物.

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    专利信息


    专利号:US-8163773-B2
    优先权日:2005-07-11
    标题 :Organic compounds
    发明人:BREITENSTEIN WERNER; ERHARDT CLAUS; MAIBAUM JUERGEN KLAUS; OSTERMANN NILS; ZIMMERMANN JUERG; MASUYA KEIICHI; KONISHI KAZUHIDE; YOKOKAWA FUMIAKI; KANAZAWA TAKANORI; JACOBY EDGAR; MARZINZIK ANDREAS; GROSCHE PHILIPP; KAWAKAMI SHIMPEI
    权利人:BREITENSTEIN WERNER; ERHARDT CLAUS; MAIBAUM JUERGEN KLAUS; OSTERMANN NILS; ZIMMERMANN JUERG; MASUYA KEIICHI; KONISHI KAZUHIDE; YOKOKAWA FUMIAKI; KANAZAWA TAKANORI; JACOBY EDGAR; MARZINZIK ANDREAS; GROSCHE PHILIPP; KAWAKAMI SHIMPEI; NOVARTIS AG
    摘要:The invention relates to 3,5-substituted piperidine compounds, these compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (=disorder) that depends on activity of renin; the use of a compound of that class for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; pharmaceutical formulations comprising a 3,5-substituted piperidine compound, and/or a method of treatment comprising administering a 3,5-substituted piperidine compound, a method for the manufacture of a 3,5-substituted piperidine compound, and novel intermediates and partial steps for its synthesis. The preferred compounds (which can also be present as salts) have the formula I wherein R1, R2, T, R3 and R4 are as defined in the specification.

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1055/s-0029-1216955
    摘要:Akamanchi K, Bellale E, Chaudhari M. A Simple, Fast and Chemoselective Method for the Preparation of Arylthiols. Synthesis. 2009 Aug 21;2009(19):3211–3. doi: 10.1055/s-0029-1216955.
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