CAS: 3459-99-2; 3-Nitrobenzimidamide

该化合物是一种有机化合物,其特点是存在一种苯环,代之以一个碳本基胺基氨基酯组和一个在元体位置的硝基苯组,其分子结构具有一种碳本基氨基氨基苯基苯基苯的功能组,以其形成氢联结的能力而闻名,有助于其在极地溶剂中的潜在再活性和溶性.硝基苯基苯组,一个强大的电排电替代体,强化了化合物的电药性,使其在各种化学反应中有用.该化合物可能展示生物活动,有可能作为药物或农用化学品合成的前体或中间体.其物理特性,如熔点和溶解性,可根据样品的具体条件和纯度而有所不同.应当查阅安全数据,因为含有硝基化合物的化合物可能很危险,可能需要小心处理.

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56406-50-9 37132-68-6 3459-66-3

上下游产品

3-nitrobenzonitrile sodium thiophenolate (3-nitrophenyl)chlorodiazirine ammonia N-acetyl-3-nitrobenzamide methyl-bis-(3-nitro-phenyl)-[1,3,5]triazine (3)H-imidazole4-benzofuran-2-yl-2-(3-nitro-phenyl)-1(3)H-imidazole N-benzoyl-3-nitrobenzamide

合成工艺路线路线简述

    📜间硝基苯腈 反应生成 3-硝基苯脒
    参考文献:Base-Catalyzed Reaction Of Nitriles With Alcohols. A Convenient Route To Imidates And Amidine Salts
    标题:Base-Catalyzed Reaction Of Nitriles With Alcohols. A Convenient Route To Imidates And Amidine Salts
    摘要:
    DOI:10.1021/jo01061A034

    海关参考信息

    供应商参考报价(招募中)

    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

    参考标题:Cui-Catalyzed Amination Of Arylhalides With Guanidines Or Amidines: A Facile Synthesis Of 1-H-2-Substituted Benzimidazoles
    作者:Xiaohu Deng,Heather Mcallister,Neelakandha S. Mani |发布日期:2009.8.7
    摘要:Cui/l5 (N,N′-Dimethylethylenediamine) Proves To Be An Efficient Catalyst System For The Amination Of Arylhalides With Guanidines. The Same Catalyst System Is Then Successfully Applied To The One-Step Synthesis Of 1-H-2-Amino-Benzimidazoles Through Tandem Aminations Of 1,2-Dihaloarenes In Modest Yields. This Methodology Is Also Applicable For The Preparation Of 1-H Or 1-Substutituted 2-Aryl- Or 2-Alkyl-Benzimidazoles

    合成参考文献


    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 213.
    参考文献:10.1038/ncomms14193|10.1038/ncomms15273
    摘要:Pegoraro S, Duffey M, Otto TD, Wang Y, Rösemann R, Baumgartner R, Fehler SK, Lucantoni L, Avery VM, Moreno-Sabater A, Mazier D, Vial HJ, Strobl S, Sanchez CP, Lanzer M. Erratum: SC83288 is a clinical development candidate for the treatment of severe malaria. Nature Communications. 2017 Apr 06;8(1):15273. doi: 10.1038/ncomms15273.
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