CAS: 2550-27-8; 3-Methyl-4-Phenylbutan-2-One

该化合物是属于芳香酮类的合成有机化合物,其特征是附属于分丁酮骨干的一个联苯组,具有独特的化学和物理特性,该化合物因其作为有机合成的中间体,特别是在生产药品,香料和特殊化学品方面所发挥的作用而受到重视,其结构特征,包括甲基和苯基替代成分,有助于其反作用和多功能性,在诸如烷基化和凝聚等反应中发挥作用.该化合物的稳定性和明确界定的分子结构使它在需要精确氯酮功能的研究和工业应用方面成为一个可靠的选择.

结构式图片

上下游产品

苄基丙酮 4-Phenyl-2-Butanone 2550-26-7
3-Benzyl-3-Methylpentane-2,4-Dione 30169-43-8
3-羟基-3-甲基-4-苯基丁烷-2-酮 3-Benzyl-3-Hydroxy-Butanon-(2) 54123-76-1
2-苄基丙酸 2-Methyl-3-Phenylpropanoic Acid 1009-67-2
3-甲基-4-苯基丁烷-2-醇 3-Methyl-4-Phenylbutan-2-Ol 56836-93-2
2-Methyl-3-Phenylpropanoyl Chloride 38385-67-0
2-苄基-2-甲基-3-氧代丁酸 2-Benzyl-2-Methyl-3-Oxobutanoic Acid 2382-57-2

合成工艺路线路线简述

    📜3-甲基-4-苯基丁烷-2-醇置于chromium(Vi) Oxide体系中,化学反应生成3-甲基-4-苯基-2-丁酮
    参考文献:Reaction Of Organolithium Reagents With Allylic Alcohols
    标题:Reaction Of Organolithium Reagents With Allylic Alcohols
    摘要:
    Doi:10.1021/jo00799A002

    海关参考信息

    专利信息


    专利号:US-7094909-B2
    优先权日:2001-06-11
    标 题 :HIV protease inhibitors, compositions containing the same, their pharmaceutical uses and materials for their synthesis
    发明人:KUCERA DAVID JOHN; SCOTT ROBERT WILLIAM
    权利人:AGOURON PHARMA
    摘要:The present invention concerns processes for preparing compounds of formula (I-H), or a prodrug, pharmaceutically active metabolite, or pharmaceutically active salt or solvate thereof, n nwhich are useful as inhibitors of the HIV protease enzyme.

    专利号:CN-1174187-A
    优先权日:1996-08-20
    标题:Synthesis process of methylbenzyl acetone trihalide

    专利号:CN-1049884-C
    优先权日:1996-08-20
    标题:Synthesis process of methylbenzyl acetone trihalide

    供应商参考报价(招募中)

    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:Tan, X.; Lv, H.; Zhang, X., Science of Synthesis: Catalytic Reduction in Organic Synthesis, (2017) 1, 52.
    摘要:Parmeggiani, F.; Galman, J. L.; Montgomery, S. L.; Turner, N. J., Science of Synthesis, (2019) , 369.
    摘要:Parmeggiani, F.; Galman, J. L.; Montgomery, S. L.; Turner, N. J., Science of Synthesis, (2019) , 384.
    摘要:Parmeggiani, F.; Galman, J. L.; Montgomery, S. L.; Turner, N. J., Science of Synthesis, (2019) , 395.
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