CAS: 1191-96-4; Ethylcyclopropane

该化合物是一种循环有机化合物,其特点是环丙烷环,附着一个乙基组,其分子式为C5H10,表示其为饱和碳氢化合物,结构由三颗碳原子组成,形成环丙烷环,并另外分离两碳乙基组.乙基环丙烷是一种无色的易燃液体,在室温下呈现出一种独特的气味.该化合物在水中溶解,但在有机溶剂中溶解,碳氢化合物是典型的.该化合物对有机化学很感兴趣,可用作合成更复杂分子的建筑块.该化合物独特的环状结构有助于其再活动,特别是在涉及环菌状的反应中.乙基环丙丙烷可进行各种化学转化,包括氢化和卤化,使其在合成有机化学中成为多用途化合物.在处理该物质时,应当采取安全防范措施,因为其易燃性和与吸入或皮肤接触有潜在健康危害.

结构式图片

MSDS等安全信息

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    CAS号2100-19-8 4-Hexenal | CAS号137-32-6 2-甲基丁醇 | CAS号2566-44-1 2-环丙基乙醇 | CAS号100910-92-7 1-ethoxypentan-3-ol | CAS号20599-27-3 1-BROMO-2-PENTENE | CAS号106-98-9 正丁烯 | CAS号765-43-5 环丙甲基酮 | CAS号627-20-3 顺-2-戊烯 | CAS号64-17-5 乙醇 | CAS号627-20-3 顺-2-戊烯 | CAS号646-04-8 反-2-戊烯 | CAS号109-67-1 1-戊烯 | CAS号78-78-4 异戊烷 | CAS号563-46-2 2-甲基-1-丁烯 | CAS号109-66-0 正戊烷 | CAS号1809-10-5 3-溴戊烷 | CAS号109-68-2 2-戊烯 | CAS号584-02-1 3-戊醇 | CAS号626-87-9 1,4-二溴戊烷

    合成工艺路线路线简述

    • 合成目标产物 Ethylcyclopropane 主要起始原料 2-Cyclopropylethanol
    • (文献来源)合成步骤主要原料 2-Cyclopropylethanol
    📜2-甲基丁醇 反应生成乙基环丙烷
    参考文献:Reactions Of Alkylcyclopropanes With Bromine And With Hydrogen Bromide
    标题:Reactions Of Alkylcyclopropanes With Bromine And With Hydrogen Bromide
    摘要:
    Doi:10.1021/ja00421A024

    海关参考信息

    专利信息


    专利号:US-11161827-B2
    优先权日:2019-04-05
    标 题 :Catalytic systems for stereoselective synthesis of chiral amines by enantiodivergent radical C—H amination
    发明人:Zhang xiao-xiang; Lang kai
    权利人:TRUSTEES BOSTON COLLEGE; THE TRUSTEES OF BOSTON COLLEGE
    摘要:In one aspect, the disclosure relates to a mode of asymmetric induction in radical processes based on sequential combination of enantiodifferentiative H-atom abstraction and stereoretentive radical substitution. Also disclosed is an asymmetric system for stereoselective synthesis of strained 5-membered cyclic sulfamides via radical 1,5-C—H amination of sulfamoyl azides. The disclosed metalloradical system can control the degree and sense of asymmetric induction in the catalytic radical C—H amination in a systematic manner. The disclosed system is applicable to a broad scope of substrates with different types of C(sp 3 )—H bonds and exhibits reactivity and selectivity, providing access to both enantiomers of useful 5-membered cyclic sulfamides in a highly enantioenriched form. Also disclosed are catalysts useful in these processes. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.

    专利号:WO-2024105700-A1
    优先权日:2022-11-18
    标 题:A method for the synthesis of anthranilic amide compounds and intermediates thereof
    发明人:MALVIYA NITIN; MAL SANJIB; KLAUSENER ALEXANDER G M
    权利人:PI INDUSTRIES LTD
    摘要:The present invention discloses a method for the synthesis of a compound of formula (V) or a salt thereof, wherein, R, R1, R2, R3, R4a and R4b are as defined in the detailed description. The method further comprises the synthesis of an anthranilic diamide compound of formula (Z).

    专利号:US-2023339844-A1
    优先权日:2020-09-17
    标题:A process for the synthesis of anthranilic acid/amide compounds and intermediates thereof
    发明人:MAHAPATRA TRIDIB; PATRA PRANAB KUMAR; KLAUSENER ALEXANDER G M; MAL SANJIB; SHARMA RAJU
    权利人:PI INDUSTRIES LTD; PI INDUSTRIES LTD
    摘要:The present invention disclosed a process for the synthesis of compound of formula (Z) or a salt thereof, n n n n n n n n n n wherein, R, R 1 , R 2 , R 3 and R 10 are as defined in the detailed description. The process further comprises the synthesis of an anthranilic diamide compound of formula (I).

    专利号:US-2023339906-A1
    优先权日:2020-09-26
    标 题 :A process for the synthesis of anthranilic acid/amide compounds and intermediates thereof
    发明人:SYTHANA SURESH KUMAR; NAGLE PRAMOD; KUMAR VIJAY KUMAR; KANAWADE SHRIKANT BHAUSAHEB; CHANDRE TUKARAM NIVRUTTI; THUBE VINAYAK KISAN; PATIL PRADEEP PRAKASH; SHUKLA SHALINI; SHENDE KANTILAL BALU; PATRA PRANAB KUMAR; KLAUSENER ALEXANDER G M
    权利人:PI INDUSTRIES LTD; PI INDUSTRIES LTD
    摘要:The present invention discloses a process for the synthesis of compound of formula (VII) or a salt thereof,wherein, R, R1, R2, R3, R4a and R4b are as defined in the detailed description. The process further comprises the synthesis of an anthranilic diamide compound of formula (I).

    专利号:US-2003162992-A1
    优先权日:2001-12-14
    标 题 :Preparation of intermediates useful in the synthesis of antiviral nucleosides
    发明人:WATANABE KYOICHI A; DU JINFA
    摘要:The present invention is an efficient process for the manufacture of α-acyloxyacetaldehyde, a key intermediate in the synthesis of 1,3-oxathiolane and 1,3-dioxolane nucleosides.

    专利号:US-11999757-B2
    优先权日:2017-11-01
    标 题:Synthesis of boronate ester derivatives and uses thereof
    发明人:BOYER SERGE HENRI; HECKER SCOTT J; VERZIJL GERARDUS K M; HERMSEN PETRUS J
    权利人:MELINTA SUBSIDIARY CORP
    摘要:Disclosed herein are methods for the preparation of boronate derivatives in the synthesis of antimicrobial compounds and uses thereof. Disclosed herein includes method of making a compound of Formula (B) by reducing the ketone group of the keto-ester compound of Formula (A), and the reduction can be performed using a Ruthenium based catalyst system or using an alcohol dehydrogenase bioreduction system.

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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:Shu, X.-Z.; Pang, X., Science of Synthesis: Special Topics, (2022) 1, 428.
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