CAS: 628-12-6; 2-Methoxyethyl Carbonochloridate

该化合物是有机化合物,其特征是其氯仿功能组,附于甲基氧乙基乙酸混合物,典型的是无色的黄色液体,有独特的气味,这种化合物以活性闻名,特别是芳香剂,在有机合成中有用,特别是在培养酯和氨化物方面;在二氯甲烷和乙醚等有机溶剂中溶解,但由于其水溶性特点,溶解能力有限;氯仿组的存在使其容易水解,释放盐酸和乙醇,在与水发生反应时,安全防范对于处理这种化合物至关重要,因为它可能具有腐蚀性,并且刺激皮肤,眼睛和呼吸系统;建议在远离水分的冷,干燥地方适当储存,以保持其稳定性并防止降解.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

phosgene 2-methoxy-ethanol bis(trichloromethyl) carbonate 2-methoxyethyl carbamate bis-(2-methoxy-ethoxycarbonyl)-peroxide 7-(2-methoxy-ethoxycarbonylamino)-3-phenyl-coumarin N-Benzyl-N-benzyloxy-carbamidsaeure-(2-methoxy-ethylester)

合成工艺路线路线简述

    📜光气,乙二醇甲醚 以 甲苯 作为反应溶剂,以50%的收率获得产物2-甲氧基氯甲酸乙酯
    参考文献:基于聚乙二醇的烟碱乙酰胆碱受体同系配体.
    标题:基于聚乙二醇的烟碱乙酰胆碱受体同系配体.
    摘要:一系列同源聚乙二醇(peg)单甲醚与烟碱乙酰胆碱受体的三个配体系列缀合.制备了乙酰氨基胆碱,环状类似物 1-乙酰基-4,4-二甲基哌嗪鎓和吡啶基醚 A-84543 的缀合物.发现每个系列都对大鼠大脑皮层中的烟碱受体保持显着的亲和力,并具有多达六个 Peg 单元的系链.此类化合物是亲水性配体,可用作荧光/亲和探针和 Nachr 多价配体的模型.
    DOI:10.1016/j.Bmc.2008.10.045

    海关参考信息

    专利信息


    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:US-6632922-B1
    优先权日:1998-03-19
    标题 :Methods and compositions for controlled polypeptide synthesis
    发明人:DEMING TIMOTHY J; CURTIN SCOTT A
    权利人:UNIV CALIFORNIA
    摘要:Methods and compositions for the generation of polypeptides having varied material properties are disclosed herein. Methods include means for making self assembling amphiphilic block copolypeptides and related protocols adding oligo(ethyleneglycol) functionalized aninoacid-N-carboxyanhydrides (NCAs) to polyaminoacid chains. Additional methods include means of adding an end group to the carboxy terminus of a polyaminoacid chain by reacting an alloc-protected amino acid amide with a transition metal-donor ligand complex, thereby forming an amido-amidate metallacycle for use in further polymerization reactions. Novel compositions for use in peptide synthesis and design including five and six membered amido-containing metallacycles and block copolypeptides are also disclosed.

    专利号:EP-3070087-B1
    优先权日:2011-08-05
    标题 :Intermediates for the synthesis of cyclic p1 linkers as factor xia inhibitors

    专利号:EP-3070087-A1
    优先权日:2011-08-05
    标 题 :Intermediates for the synthesis of cyclic p1 linkers as factor xia inhibitors

    专利号:US-3998816-A
    优先权日:1973-04-16
    标题 :7-[5-N-(n-Butoxyethoxy carbonyl and 2-chloroethoxy carbonyl)-amino] cephalosporins C
    发明人:SEKI SHIGEO; ISHIMARU TOSHIYASU
    权利人:MEIJI SEIKA KAISHA
    摘要:New and useful cephem compounds derived from cephalosporin C are provided by this invention, which are valuable as intermediate for the synthesis of another bacteriocidally active cephem derivatives and which are readily extractable from its aqueous solution by means of an organic solvent and enable the cephalosporin C content in the aqueous fermentation broth filtrate to be recovered at an improved yield. Cephalosporin C present in the fermentation broth may be converted into the cephem compounds of this invention by reacting with a substituted chloroformate compound within said filtrate, and the cephem compounds so formed may then be extracted therefrom with an organic solvent. The cephem compounds of this invention further may be converted into a 7-acylamidocephalosporanic acid or 7-aminocephalosporanic acid through some successive reactions.

    专利号:US-7615634-B2
    优先权日:2003-02-10
    标题:4-aminopyrimidine-5-one derivatives
    发明人:BARTKOVITZ DAVID JOSEPH; CHU XIN-JIE; DING QINGJIE; JIANG NAN; LOVEY ALLEN JOHN; MOLITERNI JOHN ANTHONY; MULLIN JR JOHN GUILFOYLE; VU BINH THANH; WOVKULICH PETER MICHAEL
    权利人:HOFFMANN LA ROCHE
    摘要:Novel intermediate compounds are disclosed. These compounds are useful in the synthesis of 4-aminopyrimidine-5-one derivatives that inhibit cyclin-dependent kinases, in particular cyclin-dependent kinase 4 (Cdk4). The 4-aminopyrimidine-5-one derivatives and their pharmaceutically acceptable salts have antiproliferative activity and are useful in the treatment or control of cancer, in particular solid tumors.

    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

    合成参考文献


    摘要:Compound: Poly(oxy-1,2-ethanediyl), α-(chlorocarbonyl)-ω-methoxy-
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知