CAS: 2525-02-2; 4-Propylbenzene-1,2-Diol

该化合物是一种有机化合物,其芳香结构特征为:一种苯环,有两种羟基(-OH)组和一种丙基替代成分,具有两种丙基基基化合物,其存在使二醇成为二醇,它有助于极地溶剂中的溶性及其在各种化学反应中的潜在反应,例如氧化和酯化中的潜在反应.该化合物一般呈现色色色不及黄色外观,而且波动性较低.其分子结构允许氢结合,从而影响其物理特性,如沸点和熔点.4-Propyl-1-2benzenediol可能用于各种应用,包括有机合成中的中间体,用于某些药品的配制,并可能用于抗氧化剂的生产.安全数据表明,与许多苯丙基化合物一样,应对它进行处理时应谨慎,因为潜在的刺激性特性.

结构式图片

欧盟法规

REACH注册ECHA物质C&L通报

上下游产品

dihydrosafrole 4-allylguaiacol 2,2-dichloro-5-propyl-benzo[1,3]dioxole ethanol 4-propyl-1,2-phenyl diacetate dihydrosafrole 4-allyl-5-propylbenzene-1,2-diol 3-allyl-4-propylbenzene-1,2-diol

合成工艺路线路线简述

    📜丁香酚置于aluminium(III) Iodide体系中,用 正己烷 用作溶剂,化学反应 18.0H,以62%的收率获得4-丙基苯-1,2-二醇
    参考文献:吡啶改善了三碘化铝诱导的烷基邻羟基苯基醚的选择性裂解:一种通过丁香酚去甲基化制备羟基茶维醇的实用且有效的方法
    标题:吡啶改善了三碘化铝诱导的烷基邻羟基苯基醚的选择性裂解:一种通过丁香酚去甲基化制备羟基茶维醇的实用且有效的方法
    摘要:丁香酚与三碘化铝的去甲基化由于意外的氢化副反应而变得复杂.氢化通过级联去质子化,氢碘化和氢卤交换过程进行,并且可以通过提前抑制氢碘化来防止.因此开发了一种实用的去甲基化程序,通过使用吡啶作为添加剂以基本定量的收率提供羟基茶维醇.该方法对裂解烷基邻羟基苯基醚具有选择性,并且与多种官能团相容.
    Doi:10.1055/s-0035-1588889

    海关参考信息

    专利信息


    专利号:US-6252092-B1
    优先权日:1999-04-30
    标 题 :Process for synthesis of 5-alkylbenzodioxoles
    发明人:BORZATTA VALERIO; BRANCALEONI DARIO; BATTISTINI CHRISTIAN
    权利人:ENDURA SPA
    摘要:The following description refers to a new process for the synthesis of 5-alkylated benzo[1,3]dioxole, comprising the following steps in sequence: catalytic hydrogenation of 4-acylphenol; acylation; displacement catalysed by Lewis acids; treatment with an inorganic basic compound and hydrogen peroxide; reaction with alkyl dihalides or dialkoxyalkanes. n The process described herein, which yields 5-alkylbenzo[1,3]dioxoles, is economic and can be easily scaled up to industrial size.

    专利号:US-11746364-B2
    优先权日:2018-01-17
    标题 :Enzymatic synthesis of kavalactones and flavokavains
    发明人:PLUSKAL TOMÃ?S; Weng jing-ke
    权利人:WHITEHEAD INST BIOMEDICAL RES
    摘要:Disclosed are methods, compositions, proteins, nucleic acids, cells, vectors, compounds, reagents, and systems for the preparation of kavalactones, flavokavains, and kavalactone and flavokavain biosynthetic intermediates using enzymes expressed in heterologous host cells, such as microorganisms or plants, or using in vitro enzymatic reactions. This invention also provides for the expression of the enzymes by recombinant cell lines and vectors. Furthermore, the enzymes can be components of constructs such as fusion proteins. The kavalactones produced can be utilized to treat anxiety disorder, insomnia, and other psychological and neurological disorders. The flavokavains produced can be utilized to treat various cancers including colon, bladder, and breast cancers.

    专利号:WO-2013001830-A1
    优先权日:2011-06-30
    标题 :Nucleoside antibiotic derivative
    发明人:ICHIKAWA SATOSHI; MATSUDA AKIRA; OKAMOTO KAZUYA; SAKAGAMI MASAHIRO
    权利人:UNIV HOKKAIDO NAT UNIV CORP; SHIONOGI & CO; ICHIKAWA SATOSHI; MATSUDA AKIRA; OKAMOTO KAZUYA; SAKAGAMI MASAHIRO
    摘要:The present invention addresses the problem of providing a new compound having antibacterial activity. Disclosed is a compound expressing antibacterial activity, more preferably an antibacterial nucleoside compound expressing antibacterial activity by inhibiting the activity of MraY, particularly a new derivative of Pacidamycin that is an MraY inhibitor. This new derivative of Pacidamycin or a pharmaceutically acceptable salt therof solve the abovementioned problem. By means of the method of the present invention, total synthesis of natural Pacidamycin D and its derivative is achieved.

    专利号:WO-2012032085-A1
    优先权日:2010-09-10
    标题 :Synthesis of trivalent flexible frameworks with ligands comprising catechol units for functionalizing surfaces

    专利号:CN-111254151-A
    优先权日:2020-04-01
    标 题 :A catechol 1,2-dioxygenase gene and its application in the synthesis of 4-position substituted cis, cis-muconic acid

    专利号:WO-2012032084-A1
    优先权日:2010-09-10
    标 题:Synthesis of tripodal catechol derivatives having an adamantyl basic framework for functionalizing surfaces

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    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


    参考文献:10.1055/s-0035-1588889
    摘要:Tian J, Sang D, Yao M, Chen X, Li L, Zhan H, You L. Pyridine Improves Aluminum Triiodide Induced Selective Cleavage of Alkyl o-Hydroxyphenyl Ethers: A Practical and Efficient Procedure for the Preparation of Hydroxychavicol by Demethylation of Eugenol. Synlett. 2016 Sep 29;28(01):138–42. doi: 10.1055/s-0035-1588889.
    参考文献:10.1055/s-2006-958963
    摘要:Joseph B, Popowycz F, Bernard P, Raboisson P. Synthesis of 8-Substituted Pyrazolo[1,5-a]-1,3,5-triazine Derivatives by Palladium-Catalyzed Cross-Coupling Reactions. Synthesis. 2007 Feb;2007(3):367–74. doi: 10.1055/s-2006-958963.
    参考文献:10.1055/s-2008-1032094
    摘要:Quideau S, Pouységu L, Deffieux D. Oxidative Dearomatization of Phenols: Why, How and What For Synlett. 2008 Feb 12;2008(04):467–95. doi: 10.1055/s-2008-1032094.
    参考文献:10.1055/s-0036-1588755
    摘要:Sang D, Wang J, Zheng Y, He J, Yuan C, An Q, Tian J. Carbodiimides as Acid Scavengers in Aluminum Triiodide Induced Cleavage of Alkyl Aryl Ethers. Synthesis. 2017 Mar 14;49(12):2721–6. doi: 10.1055/s-0036-1588755.
    参考文献:10.1055/a-1783-0751
    摘要:Klahn P, Zscherp R, Jimidar CC. Advances in the Synthesis of Enterobactin, Artificial Analogues, and Enterobactin-Derived Antimicrobial Drug Conjugates and Imaging Tools for Infection Diagnosis. Synthesis. 2022 May 17;54(16):3499–557. doi: 10.1055/a-1783-0751.
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