CAS: 115198-80-6; Tert-Butyl (Oxiran-2-Ylmethyl)Carbamate

该化合物是化学化合物,其结构特征包括一个异丁基化合物组,一个氨基甲酸功能组和一种亚氧(氧气)混合物.该化合物一般无色可粉黄黄色液体或固态,取决于其纯度和具体条件.该化合物因其具有反作用性而闻名,因为它存在环氧环,可以经受环状反应,从而在各种有机合成应用中发挥作用.该异丁基化合物组有助于其阻塞性,影响其有机溶剂的再活动性和溶解性.此外,该化合物的功能可参与氢的结合,影响其物理特性以及与其他分子的相互作用.该化合物可被用于合成药品,农业化学品或有机反应的中间体,突出其在化学研究和工业应用中的重要性.应参考安全数据,以便处理和储存,如所有化学物质一样.

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161513-47-9 149057-20-5 14321-26-7

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N-tert-butoxycarbonylprop-2-en-1-amine tert-butyl dicarbonatedi-tert-butyl dicarbonate tert-butyl N-(2,3-dihydroxypropyl)carbamate tert-butyl-3-chloro-2-hydroxypropylcarbamate5,14-dibenzyl-1,18-bis(tert-butoxycarbonyl)-3,16-dihydroxy-1,5,14,18-tetraaza°Ctadecane rac-1-(N-tert-Butoxycarbonylamino)-2-hydroxy-3-phenoxypropane -2,3-dihydroxypropane(S)-1-(tert-butoxycarbonyl)amino-2,3-dihydroxypropane -2,3-dihydroxypropane(R)-1-(tert-butoxycarbonyl)amino-2,3-dihydroxypropane

合成工艺路线路线简述

    📜N-(2,3-二羟基丙基)氨基甲酸叔丁酯置于吡啶,甲基磺酰氯体系中,化学反应生成N-(2-环氧乙烷基甲基)氨基甲酸酯
    参考文献:Macrocyclic Compound
    标题:Macrocyclic Compound

    海关参考信息

    专利信息


    专利号:US-8877171-B2
    优先权日:2010-02-03
    标 题 :Polyanionic multivalent macromolecules for intracellular targeting of proliferation and protein synthesis
    发明人:LICHA KAI; SCHIRNER MICHAEL; WELKER PIA; HAAG RAINER; WEINHART MARIE; PAULUS FLORIAN
    权利人:LICHA KAI; SCHIRNER MICHAEL; WELKER PIA; HAAG RAINER; WEINHART MARIE; PAULUS FLORIAN; MIVENION GMBH
    摘要:The present invention relates generally to methods and compositions for targeting of intracellular molecules involved in proliferation and protein synthesis of activated cells using polyanionic multivalent macromolecules. In particular aspect, multiple sulfate groups linked to polyol are specifically targeted to the cytoplasm and nucleus of proliferating and activated cells. The invention further comprises novel polyanionic macromolecular compounds and formulations.

    专利号:WO-2013046211-A1
    优先权日:2011-09-27
    标 题 :Processes for the preparation of 5-chloro-n-({(5s)-2-oxo-3-[4-(3-oxo-4-morpholinyl) phenyl]-1,3-oxazolidin-5-yl}methyl)-2-thiophene-carboxamide and intermediates thereof
    发明人:MOHAN RAO DODDA; KRISHNA REDDY PINGILI; VENKAT REDDY BUTHUKURI
    权利人:SYMED LABS LTD; MOHAN RAO DODDA; KRISHNA REDDY PINGILI; VENKAT REDDY BUTHUKURI
    摘要:TThe present invention provides processes for the preparation of 5-chloro-N-({(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-1,3-oxazolidin-5-yl}methyl)-2-thiophene-carboxamide (I) and intermediates thereof. Also provides novel intermediates and their use in the synthesis of oxazolidine derivatives.

    专利号:US-8431714-B2
    优先权日:2007-04-16
    标题:Synthesis of drug conjugates via reaction with epoxide-containing linkers
    发明人:MCKENNA CHARLES E; KASHEMIROV BORIS A; BALA JOY LYNN F
    权利人:MCKENNA CHARLES E; KASHEMIROV BORIS A; BALA JOY LYNN F; UNIV SOUTHERN CALIFORNIA
    摘要:The present invention relates to drug derivatives and linkers. The invention specifically relates to compounds and methods of phosphonates and linkers, that are useful as carriers for imaging agents and useful in the treatment of various bone diseases.

    专利号:US-2008312440-A1
    优先权日:2007-04-16
    标 题:Synthesis of drug conjugates via reaction with epoxide-containing linkers

    专利号:US-2005215801-A1
    优先权日:2002-06-28
    标 题 :Process for preparation of optically active 1-substituted amino-2,3-epoxypropanes, intermediates for synthesis thereof and process for preparation of the intermediates
    发明人:KITAJIMA KUMI; NAGASHIMA NOBUO
    权利人:KITAJIMA KUMI; NAGASHIMA NOBUO
    摘要:The present invention provides an industrial process for effectively and advantageously preparing optically active 1-substituted amino-2,3-epoxypropanes useful as intermediates for preparing agricultural chemicals and medical products from optically active 1-substituted amino-2,3-propanediols used as raw materials. The present invention also provides useful intermediates. Specifically, an optically active 1-substituted amino-2,3-propanediol (1) is reacted with an orthoacid ester (2) or thionyl chloride (3) to produce a cyclic optically active compound (4), and then a compound (5) containing a halogen atom is prepared by reaction with a ring-opening reaction agent having an ability to introduce a halogen atom X. Finally, an optical active 1-substituted amino-2,3-epoxypropane is prepared by ring-closure reaction in the presence of a base.

    专利号:US-2013203998-A1
    优先权日:2007-04-16
    标题:Synthesis of Drug Conjugates Via Reaction With Epoxide-Containing Linkers

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    📌 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:Spitzner, D., Science of Synthesis Knowledge Updates, (2016) 1, 330.
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