CAS: 19398-88-0; Cis-4-Decene

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    CAS号1126420-73-2 cis-2-hexenyl t... | CAS号693-04-9 正丁基氯化镁 | CAS号2384-86-3 4-癸炔 | CAS号43216-19-9 tributyl(butyli... | CAS号66-25-1 正己醛 | CAS号109-67-1 1-戊烯 | CAS号19398-89-1 反式-4-癸烯 | CAS号72612-74-9 trans-5-bromo-5... | CAS号3728-50-5 butylidene(trip... | CAS号106445-91-4 butylidenetri(f... | CAS号19398-89-1 反式-4-癸烯

    合成工艺路线路线简述

    • 合成目标产物 Cis-4-Decene 主要起始原料 4-Decyne
    • (文献来源)合成步骤主要原料 4-Decyne
    📜4-癸炔置于喹啉,氢气体系中,用 甲苯 用作溶剂,化学反应 2.5H,反应生成顺式-4-癸烷
    参考文献:转移加氢条件下炔烃选择性ru催化半还原为z烯烃
    标题:转移加氢条件下炔烃选择性ru催化半还原为z烯烃
    摘要:通过使用一种容易获得的,空气和水分稳定的二氢-Ru络合物,可以在转移加氢条件下以甲酸为氢源获得各种z烯烃,并具有出色的收率和z / E选择性.
    Doi:10.1002/chem.201001143

    海关参考信息

    专利信息


    专利号:US-5358860-A
    优先权日:1993-04-05
    标题:Stereoselective epoxidation of alkenes by chloroperoxidase
    发明人:HAGER LOWELL P; ALLAIN ERIC J
    权利人:UNIV ILLINOIS
    摘要:A method of converting olefins to chiral epoxides comprises combining an asymmetric aliphatic or aryl alkene substrate with a buffered chloroperoxidase solution to form a stabilized reaction mixture, and gradually adding hydrogen peroxide as a substrate oxidant, such that the chloroperoxidase catalyzes the conversion of the substrate to the corresponding epoxide in enantiomeric excess. The products of the invention are alkyl and aryl non-primary epoxides. The resulting preparations are enantiomerically pure, and may greatly enhance large-scale synthesis of stereoisomer products such as pharmaceuticals and pesticides.

    专利号:JP-5568470-B2
    优先权日:2007-06-13
    标 题:Process for the synthesis of diacids or diesters from natural fatty acids and / or esters

    专利号:JP-2010529180-A
    优先权日:2007-06-13
    标 题:Process for the synthesis of diacids or diesters from natural fatty acids and / or esters

    专利号:ES-2394263-T3
    优先权日:2008-07-10
    标题 :Synthesis procedure of omega-amino-alkanoic acids or their esters from natural fatty acids

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1007/s00248-017-0947-5
    摘要:Strobel G, Ericksen A, Sears J, Xie J, Geary B, Blatt B. Urnula sp., an Endophyte of Dicksonia antarctica, Making a Fragrant Mixture of Biologically Active Volatile Organic Compounds. Microb Ecol. 2017 Aug;74(2):312–21. doi: 10.1007/s00248-017-0947-5.
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