CAS: 1200-14-2; 4-Butylbenzaldehyde

该化合物是一种芳烃性甲醚,其分子式为C11H14O,其特点是在苯甲二烯环的副位置上有一个丁基替代物,该化合物通常用作有机合成的中间体,特别是在生产药品,农用化学品和芳香时使用,其结构具有芳香性甲醚的典型反应性,有利于在凝聚和氧化反应中应用.丁基组增强亲性,使其在非极溶剂中需要溶解的配方中有用. 4-丁基苯甲二烯因其在标准储存条件下的一贯纯度和稳定性而受到重视,确保合成工艺的可靠性能. 适当的处理应遵循关于甲醚的标准安全议定书.

结构式图片

物理性质

MSDS等安全信息

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

1-butyl-4-(chloromethyl)benzene bis(2-chloromethyl)ether 1-butylbenzene oxalyl dichloride p-Butylzimtsaeure 1-butyl-4-(chloromethyl)benzene 2,5-bis(4-butylphenyl)thiazolo[5,4-d]thiazole

合成工艺路线路线简述

    📜丁苯置于palladium On Activated Charcoal 三氯化铝,氢气体系中,用 三氯乙烯 用作溶剂,化学反应 1.0H,反应生成4-N-丁基苯甲醛
    参考文献:直链4-烷基苯甲醛的合成
    标题:直链4-烷基苯甲醛的合成
    摘要:描述了通过不同方法制备不含位置和支链异构体的直链4-烷基苯甲醛的方法.报道了醛的一步制备,其涉及在pd / C催化剂存在下将friedel Craft'S配合物直接氢化.
    Doi:10.1002/hlca.19820650810

    海关参考信息

    专利信息


    专利号:US-6531625-B2
    优先权日:2000-09-08
    标题 :Cinnamic esters
    发明人：KUHN WALTER; BRAUN GERHARD; KLEIN STEPHAN
    权利人:HAARMANN & REIMBER GMBH
    摘要:In a novel process for the synthesis of cinnamic esters or substituted cinnamic esters, carboxylic esters are reacted, by condensation, with benzaldehyde or substituted benzaldehydes, respectively, in the presence of a solid with basic properties.

    专利号:WO-0053313-A2
    优先权日:1999-03-09
    标 题:Lanthanide catalysts for synthesis of compounds and combinatorial libraries

    专利号:US-8558012-B2
    优先权日:2009-03-02
    标 题:2-fluoro-1,3-benzodithiol 1,1,3,3-tetraoxide derivative, production method thereof, and production method of monofluoromethyl group-containing compound using the same
    发明人：SHIBATA NORIO
    权利人:SHIBATA NORIO; NAGOYA INST TECHNOLOGY; TOSOH P TECH INC
    摘要:A 2-fluoro-1,3-benzodithiol 1,1,3,3-tetraoxide derivative as a monofluoromethyl group introduction agent that is effective as an intermediate in pharmaceutical and agrochemical synthesis, a production method thereof, and a production method of a monofluoromethyl group-containing compound using this 2-fluoro-1,3-benzodithiol 1,1,3,3-tetraoxide derivative are provided. The 2-fluoro-1,3-benzodithiol 1,1,3,3-tetraoxide derivative represented by the following general formula (1) (wherein R 1 , R 2 , R 3 , and R 4 each independently represent a hydrogen atom, a straight-chain or branched alkyl group having 1 to 4 carbon atoms, a straight-chain or branched alkyloxy group having 1 to 4 carbon atoms, a halogen atom, a nitro group, or a cyano group), the production method thereof, and various monofluoromethyl group-containing compounds are manufactured using this 2-fluoro-1,3-benzodithiol 1,1,3,3-tetraoxide derivative as a monofluoromethylating agent.

    专利号:EP-0706089-A3
    优先权日:1994-10-05
    标 题 :Process for the synthesis of a quinonediazide ester and positive working photoresist containing it

    专利号:CN-106866543-A
    优先权日:2017-04-16
    标题:A kind of method that catalyzes the synthesis of benzimidazole compound under microwave irradiation in aqueous phase

    专利号:CN-103319344-B
    优先权日:2013-06-06
    标 题:Synthesis of 1,1-Diacetate Catalyzed by Sulfonated Cage Mesoporous Carbon

    其他信息查阅

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    实用工具

    ⚠️全国化工行业净网倡议书
    📋制造商识别码
    📖 海关编码查询
    📝MSDS生成器

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Synthesis Of Novel 5,6-Dehydrokawain Analogs As Osteogenic Inducers And Their Action Mechanisms
    作者:Momochika Kumagai,Keisuke Nishikawa,Takashi Mishima,Izumi Yoshida,Masahiro Ide,Keiko Koizumi,Munetomo Nakamura,Yoshiki Morimoto |发布日期:2017.6
    摘要:Protein (Bmp) And Activation Of P38 Mapk Signaling Pathways. Compounds 14 And 21 Also Inhibited Rankl-Induced Osteoclast Differentiation Of Raw264 Cells. These Results Indicated That Novel 5,6-Dehydrokawain Analogs Not Only Increase Osteogenic Activity But Also Inhibit Osteoclast Differentiation, And Could Be Potential Lead Compounds For The Development Of Anti-Osteoporosis Agents.

    合成参考文献


    摘要:Lemière, G.; Clayden, J., Science of Synthesis Knowledge Updates, (2011) 4, 151.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知