CAS: 15485-65-1; 2-(4-Hydroxyphenyl)-1-(2,4,6-Trihydroxyphenyl)Ethanone

该化合物是一种专门的芬诺克酮化合物,在有机合成和制药研究中应用.其结构包括氢氧基和丙烯苯酮功能组,使它成为合成花草类,多酚和其他生物活性分子的宝贵中间体.该化合物由于其苯丙基氢氧基组而表现出显著的反活动性能,为有选择地调整定向衍生提供了条件.其高纯度和稳定性在标准条件下确保了研究环境的可靠性能.此外,其定义明确的分子特性有利于研究抗氧化剂活动和结构活动关系.该化合物对于开发新型治疗剂的药用化学作用特别大.

结构式图片

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17720-60-4 3669-41-8 487-49-0

合成工艺路线路线简述

    染料木素置于sodium Hydroxide体系中,用65%的收率获得2,4,6-三羟基苯基-4'-羟基苄基甲酮
    参考文献:Synthesis,Crystal Structure And Antimicrobial Activity Of Deoxybenzoin Derivatives From Genistein
    标题:Synthesis,Crystal Structure And Antimicrobial Activity Of Deoxybenzoin Derivatives From Genistein
    摘要:A Series Of Deoxybenzoin Derivatives From Genistein Were Synthesized And Their Structures Were Elucidated By H-1 NMR,Mass Spectral Data And Micro Analyses. The Structures Of 2,7 And 10 Were Determined By Single-Crystal X-Ray Analysis. These Obtained Compounds Were Evaluated For Their Assayed Antibacterial (Bacillus Subtilis,Escherichia Coli,Pseudomonas Fluorescence And Staphylococcus Aureus) And Antifungal (Aspergillus Niger,Candida Albicans And Trichophyton Rubrum) Activities By Mtt (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyl Tetrazolium. Bromide) Method. Most Compounds Have Displayed Comparable Antibacterial Activity Against Bacterial. On The Basis Of The Biological Results,Structure-Activity Relationships Are Discussed. (C) 2007 Elsevier Masson Sas. All Rights Reserved.
    Doi:10.1016/j.Ejmech.2007.05.013

    海关参考信息

    专利信息


    专利号:US-2009062555-A1
    优先权日:2007-08-28
    标 题 :Synthesis of Isoflavone
    发明人:HARMS ARTHUR E
    权利人:HARMS ARTHUR E
    摘要:The invention provides a process of manufacturing an isoflavone of the general formula 7 n n n n n n n n n n wherein R 1 , R 2 , R 3 , and R 4 each independently are H, OH, or an alkoxy, provided at least one of R 1 , R 2 , R 3 , and R 4 being OH, and one being alkoxy, or at least 2 groups being OH, comprising providing ketone (3) n n n n n n n n n n wherein R 1 , R 2 , R 3 , and R 4 are as stated above, combining (3) with trialkylortho formate, and a Lewis or Bronsted acid to produce the isoflavone, precipitating the isoflavone.
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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
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