CAS: 24974-73-0; (3-Chlorophenyl)Methanesulfonyl Chloride

该化合物是有机化合物,其特征是存在一个附属于氯苯基的全氟辛烷磺酸功能组,该化合物一般视其纯度和储存条件而呈现无色的黄色液体或固态,因其反应性而闻名,特别是由于该物质组可参与核循环替代反应,使其在有机合成中有用,特别是用于将磺酰胺组引入各种子体. 苯基环上存在氯会增强其电子哲学特性,便利进一步化学转化. 3-Chlorobezynzulfonyl氯化物通常会受到谨慎处理,因为它可能是腐蚀性的,可能会对皮肤,眼睛和呼吸系统造成刺激.适当的安全措施,包括使用个人防护设备,并在经过良好通风的地区或烟雾罩下工作,在与该化合物合作时至关重要.

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CAS号620-20-2 3-氯氯苄 | CAS号133067-71-7 S-(3-chloro)ben... | CAS号89782-88-7 1-(3-氯苯基)甲烷磺酰胺

合成工艺路线路线简述

    📜间氯氯苄置于盐酸体系中,用 乙醇,水,乙腈 用作溶剂,化学反应 1.0H,反应生成(3-氯苯基)甲基磺酰氯
    参考文献:通过n-氯代琥珀酰亚胺氯磺化反应从s-烷基异硫脲盐中方便,环保地合成磺酰氯
    标题:通过n-氯代琥珀酰亚胺氯磺化反应从s-烷基异硫脲盐中方便,环保地合成磺酰氯
    摘要:摘要 已经开发了一种方便,实用和环境友好的合成磺酰氯的方法.由s-烷基异硫脲盐以中等至优异的收率合成结构多样的磺酰氯,其可以容易地由易于获得的烷基卤化物或甲磺酸酯和廉价的硫脲通过n-氯代琥珀酰亚胺氯磺化制备.在大规模合成中,可以将来自"废水"的副产物琥珀酰亚胺与次氯酸钠(漂白剂)方便地转化为起始试剂n-氯琥珀酰亚胺,以使该方法具有可持续性. 已经开发了一种方便,实用和环境友好的合成磺酰氯的方法.由s-烷基异硫脲盐以中等至优异的收率合成结构多样的磺酰氯,其可以容易地由易于获得的烷基卤化物或甲磺酸酯和廉价的硫脲通过n-氯代琥珀酰亚胺氯磺化制备.在大规模合成中,可以将来自"废水"的副产物琥珀酰亚胺与次氯酸钠(漂白剂)方便地转化为起始试剂n-氯琥珀酰亚胺,以使该方法具有可持续性.
    Doi:10.1055/s-0033-1338743

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    专利信息


    专利号:EP-1836163-B1
    优先权日:2004-12-23
    标题 :Pyrrolidine derivatives for the treatment of a disease depending on the activity of renin
    发明人:BREITENSTEIN WERNER; COTTENS SYLVAIN; EHRHARDT CLAUS; JACOBY EDGAR; LORTHIOIS EDWIGE LILIANE JEANNE; MAIBAUM JUERGEN KLAUS; OSTERMANN NILS; SELLNER HOLGER; SIMIC OLIVER
    权利人:NOVARTIS AG
    摘要:Novel 3-mono-, 3,4-di- and 3,4,4,-tri-substituted pyrrolidine 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 inappropriate 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 inappropriate activity of renin; the use of a compound of that class in the treatment of a disease that depends on inappropriate activity of renin; pharmaceutical formulations comprising a said substituted pyrrolidine compound, and/or a method of treatment comprising administering a said substituted pyrrolidine compound, a method for the manufacture of said substituted pyrrolidine compounds, and novel intermediates and partial steps for their synthesis are described. The substituted pyrrolidine compounds are especially of the formula I wherein the substituents are as described in the specification.

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    合成参考文献


    参考文献:10.1055/s-0033-1338743
    摘要:Xu J, Yang Z. Convenient and Environment-Friendly Synthesis of Sulfonyl Chlorides from S-Alkylisothiourea Salts via N-Chlorosuccinimide Chlorosulfonation. Synthesis. 2013 May 15;45(12):1675–82. doi: 10.1055/s-0033-1338743.
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