CAS: 21423-81-4; 3-Chloro-4-Methylbenzonitrile

该化合物是一种多用途芳香硝酸化合物,其特点是在苯环上存在氯和甲基替代物,其分子结构C8H6ClN适合于有机合成的应用,特别是作为制药,农用化学品和特殊化学品的中间体.电离硝酸盐组和氯甲基替代模式增强了其在交叉反应,核分裂生物替代和循环过程中的再活动性.该化合物具有高度纯度和稳定性,适合精确的合成应用.其明确界定的化学特性促进了受控的功能化,促进了其在复杂分子结构开发中的实用性.

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CAS号67952-93-6 3-氯-4-甲基苄胺 | CAS号143-33-9 氰化钠 | CAS号95-74-9 3-氯对甲苯胺 | CAS号5162-82-3 3-氯-4-甲基苯甲酸 | CAS号21924-83-4 4-溴甲基-3-氯苯腈 | CAS号25539-20-2 2-苯氧基对苯二甲酸 | CAS号24377-95-5 3-氯-4-甲基苯甲酰胺 | CAS号67952-93-6 3-氯-4-甲基苄胺 | CAS号3411-03-8 3-氯-4-甲基苯甲醛 | CAS号106269-39-0 9-oxoxanthene-3... | CAS号863868-32-0 4-甲基-3-(4,4,5,5... | CAS号500024-78-2 (Z)-3-氯-N-羟基-4-甲基苯脒 | CAS号58588-64-0 3-氯-4-甲酰基苯甲腈

合成工艺路线路线简述

    3-Chloro-4-Methyl-N,N-Dichlorobenzylamine置于三乙胺体系中,用 二氯甲烷 用作溶剂,以89%的收率获得3-氯-4-甲基苯甲腈
    参考文献:The N-Chlorination Of Primary Amines Using Fecl3 And M-Cpba
    标题:The N-Chlorination Of Primary Amines Using Fecl3 And M-Cpba
    摘要:采用m-Cpba作为氧化剂,Fecl3作为氯源,在0oc下成功实施了一种从伯胺合成n,N-二氯胺的简单有效方法.此外,N,N-二氯胺能够以非常好产率转化为腈类或n-氯亚胺.
    Doi:10.1246/cl.130883

    海关参考信息

    专利信息


    专利号:US-7951827-B2
    优先权日:2005-05-05
    标 题:Synthesis and antiprotozoal activity of dicationic 3,5-diphenylisoxazoles
    发明人:TIDWELL RICHARD R; BAKUNOVA SVETLANA M; BAKUNOV STANISLAV; PATRICK DONALD A
    权利人:UNIV NORTH CAROLINA
    摘要:Novel dicationic 3,5-diphenylisoxazole compounds are described. Synthetic routes to these novel compounds are provided. Several of the compounds displayed in vitro activity versus Trypanosoma brucei brucei and Plasmodium falciparum comparable to that of furamidine. A majority of the novel compounds also were less toxic to VERO cells than furamidine.

    专利号:US-7569606-B2
    优先权日:2006-01-26
    标 题 :Platinum complexes with mononitrile-containing ligands
    发明人:XIAO ZEJUN; HAUSHEER FREDERICK H; PETLURU PAVANKUMAR
    权利人:BIONUMERIK PHARMACEUTICALS INC
    摘要:Disclosed herein are novel platinum-based complexes possessing one nitrile substituent group (mononitrile) covalently-bonded to the platinum, one or more nitrogen donor ligands capable of forming hydrogen bonds with the bases in DNA or RNA and leaving groups (i.e., L 1 and L 2 )which can be hydrolyzed iii vivo to active species, which can then form coordinate adducts with DNA or RNA at the Guanine or Adenine bases thereof. Also disclosed herein are the reaction schemes for the synthesis of said platinum complexes, as well as methods of treatment of various types of cancer by the administration of a pharmaceutically-effective dose of said novel platinum complexes.

    专利号:US-9550757-B2
    优先权日:2010-03-05
    标题:Nuclear transport modulators and uses thereof
    发明人:SHACHAM SHARON; KAUFFMAN MICHAEL; SANDANAYAKA VINCENT P; SHECHTER SHARON
    权利人:KARYOPHARM THERAPEUTICS INC
    摘要:The invention generally relates to the field of nuclear transport modulators, e.g., CRM1 inhibitors, and more particularly to new substituted-heterocyclic azole compounds, the synthesis and use of these compounds and their pharmaceutical compositions, e.g., in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity such as in treating cancer and other neoplastic disorders, inflammatory diseases, disorders of abnormal tissue growth and fibrosis including cardiomyopathy, pulmonary fibrosis, hepatic fibrosis, glomerulonephritis, and other renal disorders, and for the treatment of viral infections (both acute and chronic).

    专利号:CN-111170991-B
    优先权日:2014-07-11
    标题 :Antiproliferative compounds and methods of synthesis thereof

    专利号:EA-014940-B1
    优先权日:2005-08-25
    标题 :Condensed Derivatives of Imidazole to Inhibit Aldosterone Synthesis and Aromatics

    专利号:CN-111170991-A
    优先权日:2014-07-11
    标 题:Antiproliferative compounds and methods of synthesis thereof
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    合成参考文献


    参考文献:10.1107/s1600536811034751
    摘要:Cole JM, Aherne CM, Howard JA, Banister AJ, Waddell PG. The 4-(3-chloro-4-methyl-phen-yl)-1,2,3,5-dithia-diazol-3-yl radical. Acta Crystallogr Sect E Struct Rep Online. 2011 Sep 01;67(Pt 9):o2514.
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