CAS: 577-56-0; 2-Acetylbenzoic Acid

该化合物是一种有机化合物,其特点是苯环上的乙酰和箱状酸功能组群,这种多用途中间体广泛用于制药和精化合成,特别是在生产七环化合物和活性药物成分(API)时,它具有选择性的再反应作用,有利于在凝聚,循环和衍生反应中应用.该化合物在普通有机溶剂中表现出良好的溶性,便于在多步骤合成工艺中使用.在标准条件下,由于有明确界定的熔点和稳定性,2-乙酰苯甲酸是需要精确分子修改的研究和工业应用的可靠试剂.

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合成工艺路线路线简述

    📜2-乙酰基苯甲醛置于sodium Chlorite,Sodium Dihydrogenphosphate,双氧水体系中,用 水,乙腈 作为反应溶剂,化学反应生成 2-乙酰苯甲酸
    参考文献:H4Siw12O40催化三组分串联反应合成3,3-二取代异吲哚啉酮
    标题:H4Siw12O40催化三组分串联反应合成3,3-二取代异吲哚啉酮
    摘要:开发了ah 4 Siw 12 O 40催化的2-酰基苯甲酸,伯胺和氧化膦的三组分串联反应以形成3,3-二取代异吲哚啉酮.通过使用 H 4 Siw 12 O 40作为催化剂和碳酸二甲酯 (Dmc) 作作为反应溶剂,各种 2-酰基苯甲酸衍生物和伯胺都能很好地产生 C3-膦酰基官能化的 3,3-二取代异吲哚啉酮收率范围为61%-87%.这种转化的优点包括绿色催化剂和溶剂,可用的起始原料,广泛的底物范围,高效率和操作简单,水作为唯一的副产物.该策略实现了高效,绿色的分子片段组装来获取异吲哚啉酮,这将为以绿色方式合成潜在的生物活性分子提供机会.
    DOI:10.1016/j.Cclet.2023.108480

    海关参考信息

    专利信息


    专利号:US-6180830-B1
    优先权日:1995-11-08
    标题 :Method for preparing a bimetallic ruthenium/tin catalyst and a process for the synthesis of aldehydes
    发明人:JACQUOT ROLAND
    权利人:RHODIA CHIMIE SA
    摘要:The present invention relates to a new process for the preparation of a bimetallic ruthenium/tin catalyst. The process for the preparation of a bimetallic ruthenium/tin catalyst according to the invention is characterised by the fact that it consists in carrying out the reduction of a ruthenium complex having an electrovalency of -4 and a coordination number of 6, the ligands being either a halogen atom or an anion or a tin halide. The catalyst is further employed for the preparation of aldehydes by reduction, in the vapor phase, of carboxylic acids, esters and anhydrides.

    专利号:US-2004110228-A1
    优先权日:2002-04-01
    标 题:Combinatorial organic synthesis of unique biologically active compounds
    发明人:MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
    摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

    专利号:US-9006371-B1
    优先权日:2010-09-28
    标题 :Synthesis of oligomeric silsesquioxane monomers for high performance polymers
    发明人:WRIGHT MICHAEL E; PETTEYS BRIAN J; GUENTHNER ANDREW J; TOMCZAK SANDRA J
    权利人:WRIGHT MICHAEL E; PETTEYS BRIAN J; GUENTHNER ANDREW J; TOMCZAK SANDRA J; US NAVY
    摘要:A formulation and methods for making formulation of a series of oligomeric silsesesquioxane (OS) diamine monomers which have been synthesized and purified in a highly time, energy, and atom efficient manner.

    专利号:US-11584772-B2
    优先权日:2017-09-12
    标 题 :N4-modified cytidine nucleotides and their use
    发明人:MESKYS ROLANDAS; JAKUBOVSKA JEVGENIJA; TAURAITE DAIVA
    权利人:UNIV VILNIUS
    摘要:Disclosed are W-position modified cytidine nucleotides of formula (I). Provided herein are methods of chemical synthesis of AP-modified cytidine nucleoside triphosphates and their applications as well as uses of the cytidine analogues for the synthesis of modified nucleic acids. The nucleic acid molecule includes DNA, RNA or a combination of DNA/RNA. One of many applications of modified cytidine nucleotides described herein is enzyme selection, when an enzyme of interest bears an activity of an esterase, amidase, oxidoreductase, lyase, ligase or other enzymatic activity, formula (I) wherein the substituants are as defined in the appended claims.

    专利号:US-11884628-B2
    优先权日:2019-05-16
    标题 :Method for synthesizing lactam derivatives without use of catalyst
    发明人:YANG SONG; LI HU; WU HONGGUO
    权利人:UNIV GUIZHOU
    摘要:Disclosed is a simple synthesis method of lactam derivatives, comprising: with formamide functioning as both an amine source and a hydrogen source (hydrolyzed to produce formic acid), carrying out a cycloamination reaction on a raw material keto acid in the absence of a solvent or a catalyst to simply synthesize a lactam derivative. Compared with previous reports, the present disclosure has the following advantages: the time required for the reaction is greatly shortened, the selectivity is remarkably improved, a conversion rate of a keto acid derivative is greater than 99%, and the yield of the lactam derivative can reach 70% to 94%.

    专利号:WO-2024077009-A1
    优先权日:2022-10-03
    标题 :Functionalized macromolecules and systems, methods of synthesis, and uses thereof
    发明人:XIA HONGWEI; O'BRIEN EVAN; FABER-RICO JACOB; STOLARCZYK CRAIG; SIDDIQUI ASIM; YASUN EMIR; HOSSEINI NASSAB NILOUFAR
    权利人:SEER INC
    摘要:Disclosed herein are macromolecules, compositions thereof, and methods of making the same. In one aspect, the macromolecule are immobilized to a surface. In one aspect, provided herein are compositions, systems and kits comprising the macromolecules.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: Yashpal S Chhonker, Et Al. Simultaneous Quantitation Of Acetylsalicylic Acid And Clopidogrel Along With Their Metabolites In Human Plasma Using Liquid Chromatography Tandem Mass Spectrometry. Biomed Chromatogr. 2016 Mar;30(3):466-73.

    合成参考文献


    摘要:Zhang, M.; Su, W., Science of Synthesis: Catalytic Transformations via CH Activation, (2015) 1, 96.
    摘要:E. T. Harper and M. L. Bender, J. Am. Chem. Soc. 87, 5625 (1965).
    摘要:L. G. Bray, J. F. J. Dippy and S. R. C. Hughes, J. Chem. Soc. 1957, 265.
    参考文献:10.1107/s1600536810021094
    摘要:Fixler DE, Newman JM, Lalancette RA, Thompson HW. 3-Acetyl-benzoic acid. Acta Crystallogr Sect E Struct Rep Online. 2010 Jun 05;66(Pt 7):o1595.
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