CAS: 6304-89-8; 3-Acetoxybenzoic Acid

该化合物是疼痛和炎症的媒介.此外,阿司匹林因抗血脂效应而闻名,有助于心血管疾病的预防.然而,它可导致气肠道肠道和丙酮类等有机溶剂的溶解剂在水中溶解,并且应在某种化学性水平上使用.

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上下游产品

(3R,4S,5R)-3,4,5-triacetoxycyclohex-1-ene-1-carboxylic acid acetic anhydride 3-Carboxyphenol acetyl chloride 3-Methoxybenzoic acid 3-acetoxy-benzoic acid-anhydride 3-(chlor°Carbonyl)phenyl acetate Cyclohexanecarboxylic acid

合成工艺路线路线简述

    📜乙酸间甲苯酯置于cobalt(II) Acetate,Manganese(II) Acetate 偶氮二异丁腈,氧气,1,3,5-三羟基-1,3,5-三嗪-2,4,6(1H,3H,5H)-三酮体系中,用 溶剂黄146 作为反应溶剂,100.0 °C,101.32 Kpa 条件下,反应 14.0H,以75%的收率获得产物间乙酰苯甲酸
    参考文献:在n,N',N'-三羟基异氰尿酸作为关键催化剂的存在下,用分子氧氧化取代的甲苯.
    标题:在n,N',N'-三羟基异氰尿酸作为关键催化剂的存在下,用分子氧氧化取代的甲苯.
    摘要:发现n,N',N''-三羟基异烟酰胺酸(thica)是用二氧氧化烷基苯的非常有效的催化剂.因此,在thica(5 Mol%)和co(oac)存在的情况下,在o(2)(1 Atm)下,各种带有吸电子取代基的间位和对位取代甲苯,例如氰基甲苯,氯甲苯和甲苯酸)(2)(0.5 Mol%)在100摄氏度下几乎以定量收率平滑地氧化为相应的苯甲酸.比较了thica和n-羟基邻苯二甲酰亚胺对甲苯的需氧氧化.在温和的条件下,对甲苯被thica有效地高产率(超过95%)氧化为对苯二甲酸.
    DOI:10.1021/jo034313Z

    海关参考信息

    专利信息


    专利号:US-8481501-B2
    优先权日:2004-05-28
    标 题 :Synthesis of metabolically stable analgesics, pain medications and other agents
    发明人:CASHMAN JOHN R; MACDOUGALL JAMES M
    权利人:CASHMAN JOHN R; MACDOUGALL JAMES M; HUMAN BIOMOLECULAR RES INST
    摘要:Disclosed are analgesic-related compositions and methods of using the compositions for modulation of analgesic receptor activity. The compositions and methods are useful for reducing pain, as well as for therapeutic intervention of addictions or other diseases or disorders amenable to treatment or prophylaxis by modulation of analgesic receptor signaling.

    专利号:AU-2005249508-A1
    优先权日:2004-05-28
    标题 :Synthesis of metabolically stable analgesics, pain medications and other agents

    专利号:WO-2005117589-A1
    优先权日:2004-05-28
    标题:Synthesis of metabolically stable analgesics, pain medications and other agents

    专利号:JP-2008501036-A
    优先权日:2004-05-28
    标题 :Metabolic stable analgesics, pain pharmacotherapy and synthesis of other substances

    专利号:JP-2012254984-A
    优先权日:2004-05-28
    标题 :Metabolic stable analgesics, pain pharmacotherapy and synthesis of other substances

    专利号:EP-1758452-A4
    优先权日:2004-05-28
    标题:SYNTHESIS OF METABOLIC STABLE ANALGETICS, DISEASES OF MEDICAMENTS AND OTHER ACTIVE SUBSTANCES

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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

    主要参考文献

    参考标题:Pcn Pincer Palladium(II) Complex Catalyzed Enantioselective Hydrophosphination Of Enones: Synthesis Of Pyridine-Functionalized Chiral Phosphine Oxides As NcSp3O Pincer Preligands
    作者:Xin-Qi Hao,Juan-Juan Huang,Tao Wang,Jing Lv,Jun-Fang Gong,Mao-Ping Song |发布日期:2014.10.17
    摘要:A Series Of Chiral Pcn Pincer Pd(II) Complexes Vi-Xiii With Aryl-Based Aminophosphine-Imidazoline Or Phosphinite-Imidazoline Ligands Were Synthesized And Characterized. They Were Examined As Enantioselective Catalysts For The Hydrophosphination Of Enones. Among Them, Complex Ix, Which Features A Ph2Po Donor As Well As An Imidazoline Donor With (4S)-Phenyl And N-Tol-P Groups, Was Found To Be The Optimal

    合成参考文献


    摘要:Zhang, M.; Su, W., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 3, 107.
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