CAS: 18370-10-0; 3-Chloro-N-Methylbenzamide

该化合物是一种替代苯并胺衍生物,其特点是在三处有一个氯基组和氮原子上的甲基替代组.该化合物具有作为更复杂分子的构件的潜力,因此对有机合成和制药研究感兴趣.氯和甲基功能组增强了其活性,使之适合进一步衍生或作为药用化学应用的中间体.其明确界定的结构和纯度确保合成工作流程的一致性能.该化合物通常在标准实验室条件下处理,并因其卤化性质而注意适当的安全议定书.

结构式图片

欧盟法规

C&L通报

上下游产品

m-Chlorobenzoyl chloride methylamine propan-1-ol 3-chlorobenzoate H-tetrazole5-(3-chloro-phenyl)-1-methyl-1H-tetrazole 2-nitro-5-chlorobenzamide 7-methoxy-2-methyl-3,4-diphenylisoquinolin-1(2H)-one 7-chloro-2-methyl-3,4-diphenylisoquinolin-1(2H)-one

合成工艺路线路线简述

  • 合成目标产物 3-Chloro-N-Methylbenzamide ,98% 主要起始原料 3-Chlorobenzoyl Chloride And Methylamine
  • (文献来源)合成步骤主要原料 3-Chlorobenzoyl Chloride 和 Methylamine
📜3-氯苯甲酸置于乙醚,五氯化磷体系中,化学反应生成3-氯-N-甲基苯甲酰胺
参考文献:Montagne,Recueil Des Travaux Chimiques Des Pays-Bas,1900,Vol. 19,P. 55
标题:Montagne,Recueil Des Travaux Chimiques Des Pays-Bas,1900,Vol. 19,P. 55

海关参考信息

专利信息


专利号:US-10017481-B2
优先权日:2012-03-17
标 题 :Conformationally constrained, fully synthetic macrocyclic compounds
发明人:OBRECHT DANIEL; ERMERT PHILIPP; OUMOUCH SAID; PIETTRE ARNAUD; GOSALBES JEAN-FRANÇOIS; THOMMEN MARC
权利人:POLYPHOR AG
摘要:The conformationally restricted, spatially defined macrocyclic ring system of formula (I) is constituted by three distinct molecular parts: Template A, conformation Modulator B and Bridge C. Macrocycles described by this ring system I are readily manufactured by parallel synthesis or combinatorial chemistry in solution or on solid phase. They are designed to interact with a variety of specific biological target classes, examples being agonistic or antagonistic activity on G-protein coupled receptors (GPCRs), inhibitory activity on enzymes or antimicrobial activity. In particular, these macrocycles show inhibitory activity on endothelin converting enzyme of subtype 1 (ECE-1) and/or the cysteine protease cathepsin S (CatS), and/or act as antagonists of the oxytocin (OT) receptor, thyrotropin-releasing hormone (TRH) receptor and/or leukotriene B4 (LTB4) receptor, and/or as agonists of the bombesin 3 (BB3) receptor, and/or show antimicrobial activity against at least one bacterial strain. Thus they are showing great potential as medicaments for a variety of diseases.

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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

合成参考文献


摘要:Glushkov, V. A.; Shklyaev, Yu. V., Science of Synthesis Knowledge Updates, (2018) 3, 261.
摘要:Li, Y.; Fang, X.; Wang, Y., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 53.
摘要:Simmons, N.; Chheda, P.; Schuman, D., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 393.
摘要:Migliorini, F.; Puglioli, S.; Neri, D.; Cazzamalli, S.; Favalli, N., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 111.
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