CAS: 39098-75-4; 3-Cyclohexylpropanoyl Chloride

该化合物是有机化合物,其结构特征包括附于一个丙烯基氯化物功能组的环环,该化合物一般没有颜色,可粉色黄色液体,由于存在氯丙烷功能组而具有反应性,从而成为有机合成的一个有用中间体.氯丙烯丙烯可发生各种化学反应,包括杂交和核生殖替代,使其在生产药品,农用化学品和其他有机化合物方面具有价值.重要的是要谨慎地处理该物质,因为它具有腐蚀性,可能会对皮肤,眼睛和呼吸系统造成刺激.适当的安全防范措施,包括使用个人防护设备和在通风良好的地区工作,在与该化合物合作时至关重要.

结构式图片

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2719-27-9 5664-21-1 1124-62-5

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上下游产品

CAS号701-97-3 3-环己基丙酸 | CAS号1124-63-6 3-环己基-1-丙醇 | CAS号4442-79-9 2-环己基乙醇 | CAS号41010-09-7 3-cyclohexylpro... | CAS号501-52-0 3-苯丙酸 | CAS号695-12-5 乙烯基环己烷 | CAS号4441-63-8 4-环己烷丁酸 | CAS号28861-24-7 3-cyclohexyl-1-... | CAS号72299-19-5 3-cyclohexyl-N,... | CAS号72299-20-8 N,N-dibutyl-3-c... | CAS号85204-27-9 Cyclohexaneprop... | CAS号91424-53-2 N,N-di(butan-2-... | CAS号94157-86-5 phenyl cyclohex... | CAS号40435-64-1 1-cyclohexyl-4-...

合成工艺路线路线简述

    📜乙烯基环己烷置于氯化亚砜,硫酸,过氧化苯甲酰体系中,化学反应生成3-环己基丙酰氯
    参考文献:Francois,H. Et Al.,Bulletin De La Societe Chimique De France,1970,# 2,P. 617-624
    标题:Francois,H. Et Al.,Bulletin De La Societe Chimique De France,1970,# 2,P. 617-624

    海关参考信息

    专利信息


    专利号:US-11149065-B2
    优先权日:2017-04-07
    标 题:One-bead-two-compound macrocyclic library and methods of preparation and use
    发明人：CAI JIANFENG; SHI YAN
    权利人:UNIV SOUTH FLORIDA
    摘要:A one-bead-two-compound combinatorial synthesis technique provides libraries of macrocyclic peptidomimetic compounds and compositions with use as ligands for the Ephrin type-A receptor 2 (EphA2). The one-bead-two-compound technique and libraries of macrocyclic compounds are useful as research tools in drug discovery and/or to treat or prevent a range of diseases or disorders.

    专利号:US-8088923-B2
    优先权日:2006-07-07
    标题:Cyclic-fused beta-lactones and their synthesis
    发明人：ROMO DANIEL; HENRY-RIYAD HUDA; LEE CHANGSUK; NGUYEN HENRY; PUROHIT VIKRAM C; OH SEONGHO
    权利人:ROMO DANIEL; HENRY-RIYAD HUDA; LEE CHANGSUK; NGUYEN HENRY; PUROHIT VIKRAM C; OH SEONGHO; TEXAS A & M UNIV SYS
    摘要:The present invention provides a concise synthetic method for generating lactam-fused beta-lactones that feature, in some embodiments, a tertiary fused carbinol, quaternary carbons, and a reactive beta-lactone moiety available for further reactions. The present invention further provides compounds synthesized by this method as well as methods of using these compounds as inhibitors of the proteasome and fatty acid synthase.

    专利号:US-3636119-A
    优先权日:1969-10-20
    标题:4-amino-2-(8-cyclohexyloctyl or 7-cyclohexylheptyl)-1-naphthol
    发明人：FIESER LOUIS F; LORENZ ROMAN R; ARCHER SYDNEY
    权利人:FIESER LOUIS F; ROMAN R LORENZ; SYDNEY ARCHER
    摘要:4-AMINO-2-Q-1 NAPHTHOL COMPOUNDS WHICH ARE USEFUL AS INTERMEDIATES IN THE SYNTHESIS OF 2-Q-1,4-NAPHTHOQUINONE COMPOUNDS, WHERE Q IS (7-CYCLOHEXYLHEPTYL OR 8-CYCLOHEXYLOCTYL).

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    合成参考文献


    摘要:Tidwell, T. T., Science of Synthesis, (2006) 23, 601.
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