CAS: 16188-57-1; 2-Iodo-4-Methylphenol

该化合物是一种含有分子式C7H7IO的碘酚化合物.它作为有机合成的多用途中间体,特别是在生产药品,农用化学品和特殊化学品方面.碘和氢氧化物组的存在增强了其活性,使其对电益替代和交叉反应具有价值.其明确界定的结构和高纯度确保了合成应用的一贯性.该化合物通常以在标准储存条件下具有稳定性的晶状固态供应.研究人员倾向于2-Iodo-4-甲基苯酚,以便其可预测的再活动性和在构建复杂的分子框架方面的效用.建议进行适当的处理,因为其可能对光和湿度具有敏感性.

结构式图片

相似化合物

60032-63-5 2296-23-3 1948-40-9

欧盟法规

C&L通报

上下游产品

p-cresol 4,4'-dimethyl-2,2'-selanediyl-di-phenol sodium 4-methylphenoxide thallium p-cresolate 2-(2-hydroxy-5-methylphenylthio)benzoic acid 6-methylflavone (Z)-2-benzylidene-5-methylbenzofuran-3(2H)-one 2-iodo-4-methylphenyl-p-toluenesulfonate

合成工艺路线路线简述

    📜对甲酚置于sodium Hypochlorite,Sodium Iodide,Sodium Hydroxide,盐酸,Sodium Thiosulfate体系中,用 甲醇,水 用作溶剂,以62%的收率获得2-碘-4-甲基苯酚
    参考文献:铜(II)催化邻碘苯酚与芳基乙炔的多米诺合成2-芳基苯并[ B ]呋喃
    标题:铜(II)催化邻碘苯酚与芳基乙炔的多米诺合成2-芳基苯并[ B ]呋喃
    摘要:宽范围的2-芳基苯并[的b ]呋喃的合成通过分子间多米诺ç (芳基)-C ^ (炔基)键的形成,随后通过分子内ç (炔基)-ö经由铜(II)键形成的环化-催化的偶联ö-碘酚和芳基末端乙炔.该方法既不需要昂贵的钯催化剂,也不需要亲氧性膦配体,它们可以耐受不同的官能团.该方法成功地用于β-淀粉样聚集抑制剂5-氯-3-[4-(3-二乙基氨基丙氧基)苯甲酰基]-2-(4-甲氧基苯基)苯并呋喃的正式合成中.
    Doi:10.1016/j.Tet.2010.01.026

    海关参考信息

    专利信息


    专利号:US-6495693-B2
    优先权日:1996-11-22
    标题:N-(aryl/heteroaryl) amino acid derivatives, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
    发明人:AUDIA JAMES E; FOLMER BEVERLY K; JOHN VARGHESE; LATIMER LEE H; NISSEN JEFFREY S; PORTER WARREN J; THORSETT EUGENE D; WU JING
    权利人:ATHENA NEUROSCIENCES INC; LILLY CO ELI
    摘要:Disclosed are compounds which inhibit beta-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits beta-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

    专利号:US-6486350-B1
    优先权日:1998-09-30
    标 题:Biological reagents and methods for determining the mechanism in the generation of β-amyloid peptide
    发明人:AUDIA JAMES E; HYSLOP PAUL A; NISSEN JEFFREY S; THOMPSON RICHARD C; TUNG JAY S; TANNER LAURA I
    权利人:ELAN PHARM INC; LILLY CO ELI
    摘要:Disclosed are biological reagents which comprise compounds that inhibit beta-amyloid peptide release and/or its synthesis, and, accordingly, have utility in determining the cellular mechanism involved in the generation of beta-amyloid peptide.

    专利号:US-7473786-B1
    优先权日:2003-12-05
    标题:Methods and systems for preparing fused heterocyclic compounds using copper(I) catalysts
    发明人:VENKATARAMAN DHANDAPANI; BATES CRAIG G; SAEJUENG PRANORM
    权利人:UNIV MASSACHUSETTS
    摘要:A copper(I)-catalyzed procedure for the synthesis of benzo[b]heterocycles. This protocol can be used to synthesize a variety of 2-arylbenzo[b]furans and indoles in good to excellent yields. This method can tolerate a variety of functional groups, does not require the use of expensive additives and is palladium-free.

    专利号:US-6096782-A
    优先权日:1996-11-22
    标 题:N-(aryl/heteroaryl) amino acid derivatives pharmaceutical compositions comprising same and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds

    专利号:WO-9822493-A2
    优先权日:1996-11-22
    标 题:N-(ARYL/HETEROARYL) AMINO ACID DERIVATIVES, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, AND METHODS FOR INHIBITING β-AMYLOID PEPTIDE RELEASE AND/OR ITS SYNTHESIS BY USE OF SUCH COMPOUNDS

    专利号:CN-1237978-A
    优先权日:1996-11-22
    标题 :N-(aryl/heteroaryl) amino acid derivatives, pharmaceutical compositions comprising these derivatives and methods for inhibiting the release of beta-amyloid peptide and its synthesis using these compounds

    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

    参考标题:Construction Of 2-Substituted-3-Functionalized Benzofurans Via Intramolecular Heck Coupling: Application To Enantioselective Total Synthesis Of Daphnodorin B
    作者:Hu Yuan,Kai-Jian Bi,Bo Li,Rong-Cai Yue,Ji Ye,Yun-Heng Shen,Lei Shan,Hui-Zi Jin,Qing-Yan Sun,Wei-Dong Zhang |发布日期:2013.9.20
    摘要:A Novel Approach Was Developed For The Synthesis Of 2-Substituted-3-Functionalized Benzofurans, Using An Intramolecular Heck Reaction Which Was Further Applied In The First Enantioselective Total Synthesis Of Daphnodorin B.

    合成参考文献


    摘要:Kwiecień, H., Science of Synthesis Knowledge Updates, (2014) 4, 68.
    摘要:Kwiecień, H., Science of Synthesis Knowledge Updates, (2014) 4, 63.
    摘要:Dong, X.; Liu , H., Science of Synthesis Knowledge Updates, (2019) 3, .
    摘要:Solorio-Alvarado, C. R., Science of Synthesis: Hypervalent Halogens in Organic Synthesis, (2025) .
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