CAS: 4341-24-6; 5-Methylcyclohexane-1,3-Dione

该化合物是有机化合物,其特点是循环结构以及位于环环1和3位置的两个碳基(克酮)组.该化合物的特点是附于环氧环氧环乙烷第五碳的甲基组,该组有助于其独特的化学特性.该化合物一般无色可粉黄黄色液体或固体,视温度和纯度而定.碳基组的存在使其有可能成为各种化学反应,包括核循环添加和凝聚反应的候选体.此外,5-M乙基六氯环己烷-1,3-二酮可表现出自体主义,由于氢原子和双联体的转移,该化合物可能以不同的结构形式存在.该化合物对有机合成感兴趣,并可能对药品或农用化学品的发展具有应用性.与许多有机化合物一样,处理应谨慎,考虑到潜在的健康和环境影响.

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126-81-8 1193-55-1 57641-95-9

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上下游产品

orcinol diethyl ether 3-methyl-5-oxo-hexanoic acid ethyl ester sodium ethanolate t-enylidene-bis-cyclohexane-1,3-dione5,5'-dimethyl-2,2'-but-2t-enylidene-bis-cyclohexane-1,3-dione 3-methyl glutaric acid m-methylcyclohexanol 2-acetyl-5-methyl-1,3-cyclohexanedione

合成工艺路线路线简述

    📜甲基6-甲基-2,4-环己二酮羧酸酯置于水,Potassium Hydroxide体系中,化学反应生成 5-甲基环己烷-1,3-二酮
    参考文献:Partially Saturated Indeno[1,2-B]Indole Derivatives Via Deoxygenation Of Heterocyclic α-Hydroxy-N,O-Hemiaminals
    标题:Partially Saturated Indeno[1,2-B]Indole Derivatives Via Deoxygenation Of Heterocyclic α-Hydroxy-N,O-Hemiaminals
    摘要:一系列3-氨基环己烯-2-酮与单水合的吡喃-1,2,3-三酮(呋喃啉)反应,反应生成4B,9B-二羟基吲哚[1,2-B]吲哚,其后经脱氧反应转化为吲哚[1,2-B]吲哚.
    DOI:10.1055/s-0028-1087983

    海关参考信息

    专利信息


    专利号:US-6166031-A
    优先权日:1987-10-19
    标 题:Substituted tetralins, chromans and related compounds in the treatment of asthma
    发明人:EGGLER JAMES F; MARFAT ANTHONY; MELVIN JR LAWRENCE S
    权利人:PFIZER
    摘要:Substituted tetralins, chromans and related compounds which, by inhibiting 5-lipoxygenase enzyme and/or blocking leukotriene receptors, are useful in the prevention or treatment of asthma, arthritis, psoriasis, ulcers, myocardial infarction and related disease states in mammals; pharmaceutical compositions comprising said compounds; a method of treatment with said compounds; and intermediates useful in the synthesis of said compounds.

    专利号:US-6262272-B1
    优先权日:1997-11-13
    标题 :Method of synthesis of pyrrole amides
    发明人:RAGAN JOHN ANTHONY; MAKOWSKI TERESA WOODALL; AM ENDE DAVID JON; CLIFFORD PAMELA JANE; YOUNG GREGORY RANDALL; CONRAD ALYSON KAY; EISENBEIS SHANE ALLEN; QUALLICH GEORGE JOSEPH; ALLEN DOUGLAS JOHN MELDRUM
    权利人:PFIZER
    摘要:A method for preparing pyrrole-carboxyamides which selectively bind to GABAa receptors; which comprises reacting 1,3-cycloakane-diones with bromoethylacetate followed by reaction of the resulting product with an acid halide followed by reaction with an aromatic amine and finally with an amonium source at an elevated temperature.

    专利号:WO-9925684-A1
    优先权日:1997-11-13
    标题 :Method of synthesis of pyrrole amides

    专利号:EP-1030838-A1
    优先权日:1997-11-13
    标 题 :Method of synthesis of pyrrole amides

    专利号:HU-P0100235-A2
    优先权日:1997-11-13
    标题:Process for the synthesis of indole and coumarin carboxamide derivatives

    专利号:TW-509675-B
    优先权日:1997-11-13
    标 题 :Method of synthesis of pyrrole amides

    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

    主要参考文献

    [参考文献]: Xin Linghu, Et Al. Total Synthesis Of (+)-Fawcettimine. Angew Chem Int Ed Engl. 2007;46(40):7671-3.

    合成参考文献


    参考文献:10.1107/s1600536811005678
    摘要:North H, Wutoh K, Odoom MK, Karla P, Scott KR, Butcher RJ. 3-(4-Chloro-anilino)-2,5-dimethyl-cyclo-hex-2-en-1-one. Acta Crystallogr Sect E Struct Rep Online. 2011 May 01;67(Pt 5):o1283–4.
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