CAS: 4660-80-4; Ethyl Oxirane-2-Carboxylate

该化合物是一种有机化合物,其特征是其四氧化物功能组,有助于其在化学合成过程中的回活动性和多功能性.它是一种无色的黄色液体,具有甜甜的果味,可溶于乙醇和乙醚等有机溶剂,但在水中溶解性有限.该化合物主要用于合成各种药品,农用化学品,并因其能够进行环状反应而成为有机化学的一个构件.乙基甘酸盐因其在调味剂和香料生产中的潜在应用而闻名.重要的是要谨慎地处理这一化合物,因为它可能会刺激皮肤和眼睛,而且在使用过程中应当采取适当的安全防范措施.此外,该化合物被归类为一种危险物质,其处理须遵守监管准则,以确保实验室和工业环境中的安全.

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111058-33-4 57044-25-4 60456-23-7

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号140-88-5 丙烯酸乙酯 | CAS号73245-18-8 dimethyl 8'-7',... | CAS号73245-23-5 dimethyl 1'-met... | CAS号75-03-6 碘乙烷 | CAS号3999-55-1 反式-1,2-环丙烷二甲酸二乙酯 | CAS号623-72-3 3-羟基丙酸乙酯

合成工艺路线路线简述

    📜丙烯酸乙酯置于manganese(II) Sulfate,双氧水,Sodium Oxalate,草酸,1,4,7-三甲基-1,4,7-三氮杂环壬烷体系中,用 乙腈 作为反应溶剂,化学反应 2.0H,反应生成 2,3-环氧丙酸乙酯
    参考文献:在草酸盐缓冲液存在下,Mn-三甲基三氮杂环戊烷络合物催化末端或缺电子烯烃与H2O 2环氧化
    标题:在草酸盐缓冲液存在下,Mn-三甲基三氮杂环戊烷络合物催化末端或缺电子烯烃与H2O 2环氧化
    摘要:催化量的草酸盐/草酸缓冲液可大大增强mn-Tmtacn配合物与H2O 2进行环氧化反应的催化性能.特别是末端烯烃容易被环氧化.对于产量例如乙酸烯丙基酯或1-己烯分别高达99%和烯烃和过氧化基础65%.该反应是立体特异性的.没有溶剂分解的产物.
    DOI:10.1016/s0040-4039(98)00396-7

    海关参考信息

    专利信息


    专利号:US-9150840-B2
    优先权日:2011-08-26
    标题 :Isolated bacterial strain of Achromobacter sp. MTCC 5605 and a highly enantioselective epoxide hydrolase isolated therefrom
    发明人:KAMAL AHMED; KHANNA ROHINI; KUMAR CHITYAL GANESH; SHAIK ANVER BASHA; KUMAR MATAM SHIVA
    权利人:KAMAL AHMED; KHANNA ROHINI; KUMAR CHITYAL GANESH; SHAIK ANVER BASHA; KUMAR MATAM SHIVA; COUNCIL SCIENT IND RES
    摘要:The present invention relates to a novel epoxide hydrolase enzyme which aims to achieve a high degree of resolution towards a broader range of substrates with high enantioselectivity and yields with minimal product inhibition. The invention further relates to a new bacterial strain Achromobacter sp. MTCC 5605 isolated from a petroleum-contaminated sludge sample, capable of producing the said enzyme. It is notable that the enzyme can be used as whole bacterial cell preparation, which allows continuous hydrolysis of substrates at even higher concentration and have an advantage of being recycled. The invention further relates to a process for the hydrolysis of different aryl epoxides which are potential synthons of intermediates for the synthesis of chiral amino alcohols and bioactive compounds like β-blockers.

    专利号:US-8921580-B2
    优先权日:2012-05-09
    标 题 :Methods and systems for the formation of cyclic carbonates
    发明人:HATTON TREVOR ALAN; JAMISON TIMOTHY F; KOZAK JENNIFER AIDEN; SIMEON FRITZ; WU JIE
    权利人:MASSACHUSETTS INST TECHNOLOGY
    摘要:Described herein are inventive methods for synthesis of cyclic carbonates from CO 2 and epoxide. In some embodiments, the methods are carried out in the presence of a catalyst comprising an electrophilic halogen. In some embodiments, the methods are carried out in a flow reactor.

    专利号:US-2023126376-A1
    优先权日:2020-03-27
    标 题 :Synthesis of methyl 2-fluoroacrylate

    专利号:US-4638018-A
    优先权日:1983-04-11
    标 题 :Acrylic telomers with grafts which can be cross linked by light, their synthesis and their applications in coating metals
    发明人:BAUDUIN GERARD; BOUTEVIN BERNARD; DEISS WILLY-JEAN; PIETRASANTA YVES
    权利人:CEGEDUR
    摘要:PCT No. PCT/FR84/00092 Sec. 371 Date Dec. 10, 1984 Sec. 102(e) Date Dec. 10, 1984 PCT Filed Apr. 6, 1984 PCT Pub. No. WO84/04097 PCT Pub. Date Oct. 25, 1984.The invention relates to acrylic telomers with grafts which can be cross linked by light, methods of synthesizing them and their applications. The telomers comprise a telogen of the mercaptan family, in particular dodecanethiol, and links of a taxogen of the acrylic family, some of which are grafted. The telomers are synthesized semi-continuously by radical initiation in the presence of initiators such as azobisisobutyronitrile, at a temperature below 75 DEG C., making it possible to obtain a number of links adapted to the desired applications. Grafting is carried out by means of glycidyl and aziridinyl groups.

    专利号:EP-4126807-A1
    优先权日:2020-03-27
    标 题 :Synthesis of methyl 2-fluoroacrylate

    专利号:WO-2021191876-A1
    优先权日:2020-03-27
    标题:Synthesis of methyl 2-fluoroacrylate

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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


    摘要:Haufe, G., Science of Synthesis, (2005) 34, 367.
    摘要:Goeddel, D.; Shi, Y., Science of Synthesis, (2008) 37, 281.
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