CAS: 6590-97-2; 2,3-Dichlorophenylisothiocyanate

该化合物是一种多用途芳香化合物,其特点是存在二氯和异硫代亚胺功能组,其反应性异硫氰化物使该化合物成为有机合成中的宝贵中间体,特别是用于制作硫尿素衍生物和三环化合物,二氯代用品增强了其稳定性并影响其电子特性,有利于在交叉相交和核生殖替代反应中选择性反应.该化合物通常用于制药和农用化学研究,因为它在建造生物活性松子方面有用.其定义明确的再活性特征和与各种反应条件的兼容性使得它成为需要精确功能化的合成应用的一种实用选择.

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欧盟法规

ECHA物质C&L通报

上下游产品

CAS号463-71-8 硫光气 | CAS号608-27-5 2,3-二氯苯胺 | CAS号41542-06-7 1-(2,3-二氯苯基)-2-硫脲

合成工艺路线路线简述

  • 合成目标产物 2,3-Dichlorophenyl Isothiocyanate 主要起始原料 Thiophosgene And 2,3-Dichloroaniline
  • (文献来源)合成步骤主要原料 Thiophosgene 和 2,3-Dichloroaniline
📜氯甲酸乙酯置于三乙胺体系中,化学反应生成 2,3-二氯苯基硫代异氰酸酯
参考文献:Compounds With Copper-Or Zinc-Activated Toxicity Against Microbial Infection
标题:Compounds With Copper-Or Zinc-Activated Toxicity Against Microbial Infection
摘要:具有新型吡唑硫酰胺基nnsn结构基元的杂环化合物,对微生物感染具有高效的锌或铜活化毒性,在微摩尔或纳摩尔最小抑制浓度(mic)下,以及制备和使用这些化合物的方法.

海关参考信息

专利信息


专利号:US-6136984-A
优先权日:1996-04-22
标 题 :Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes
发明人:DOERWALD FLORENCIO ZARAGOZA
权利人:NOVO NORDISK AS
摘要:A solid phase method for the synthesis of a plurality of differently substituted thiophenes with a wide variety of side-chain substituents as compounds of potential therapeutic interest is disclosed. The thiophenes are prepared by acylation of a substrate-bound primary or secondary amine with cyanoacetic acid and reaction of the resulting cyanoacetamide with an isothiocyanate in the presence of a base. Alkylation with an appropriate alkyl halide, followed by Thorpe-Ziegier-cyclization yields differently substituted, support-bound 3-aminothiophenes. These may be screened on the substrate or cleaved from the substrate and then screened in solution. Alternatively, the resin-bound 3-amino thiophenes or the synthetic intermediates can be subjected to further synthetic transformations (N-acylation, reduction) on the support, which permits the preparation of further therapeutically interesting compounds. The efficient synthesis of a wide variety of thiophenes using automated synthesis technology of the present method makes these compounds attractive candidates for the generation and rapid screening of diverse thiophene-based libraries. The method disclosed here provides an easy and fast access to highly diverse heterocyclic compounds of therapeutic interest, amenable to automatization.

专利号:WO-9700244-A1
优先权日:1995-06-19
标题 :Process for parallel synthesis of a non-peptide library
发明人:FRITZ JAMES E; KALDOR STEPHEN W
权利人:LILLY CO ELI; FRITZ JAMES E; KALDOR STEPHEN W
摘要:A process for the sequential preparation of a library of compounds having pharmaceutical usage. The process involves the sequential mixing of solution phase reagents, followed by scavenging of excess unreacted reagents with solid phase scavenging agents. The process is highly iterative and applicable for producing various ureas, thiureas, amides, carbonates and tertiary amines.

专利号:WO-9740034-A1
优先权日:1996-04-22
标题:Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes

专利号:EP-1021435-A1
优先权日:1996-04-22
标题:Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes

专利号:EP-1776367-A1
优先权日:2004-07-27
标题 :Synthesis of 6,7-dihydro-5h-imidazoý1,2-a¨imidazole-3-sulfonic acid amides

专利号:WO-2006014828-A1
优先权日:2004-07-27
标题 :Synthesis of 6,7-dihydro-5h-imidazo[1,2-a]imidazole-3-sulfonic acid amides

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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


参考文献:10.1038/srep42144
摘要:Oh YJ, Kim D, Oh S, Jang EJ, Won HY, Jeong H, Jeong MG, Choo HP, Hwang ES. Novel benzoxazole derivatives DCPAB and HPAB attenuate Th1 cell-mediated inflammation through T-bet suppression. Scientific Reports. 2017 Feb 07;7(1):42144. doi: 10.1038/srep42144.
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