CAS: 5000-65-7; 2-Bromo-1-(3-Methoxyphenyl)Ethanone

该化合物是一种属于乙型苯酚类的有机化合物,具有一种溴原子和与芳香环相连的甲氧基化合物,影响其化学反应和物理特性.该化合物一般在室温中呈现为固体,其特点是在乙醇和二氯甲烷等有机溶剂中具有中等溶解性,同时由于其缺水性,在水中较不易溶解.溴原子的存在增强了其电子嗜好性,使其在各种化学反应中有用,包括核感毒替代和联动反应.甲氧氧基化合物组也可以参与电温效应,在化学变异过程中可以稳定某些中间体. 2-Bromo-3 欧元-氧乙酮苯酮经常用于有机合成,特别是在开发药品和农用化学剂时,由于其具有多种特性的再活动性,并且有能力作为化合物的建筑构件,因此,在进行更复杂的分子的处理时,应作为安全防范措施.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号586-37-8 3-甲氧基苯乙酮 | CAS号1072880-82-0 4-(3-甲氧基苯基)噁唑 | CAS号205655-28-3 2-(3-methoxyphe... | CAS号194787-90-1 2-氨基-4-(3-甲氧基苯基... | CAS号83558-37-6 4-(3-甲氧基苯基)-噻唑-2-胺 | CAS号86358-29-4 3-甲氧基苯甲酰基甲酸乙酯 | CAS号586-37-8 3-甲氧基苯乙酮 | CAS号1017395-60-6 2-(3-甲氧基苯基)吗啉 | CAS号32017-77-9 2-(间甲氧基苯基)环氧乙烷 | CAS号2491-37-4 2-溴-3'-羟基苯乙酮 | CAS号18927-05-4 3-甲氧基苯乙酸甲酯

合成工艺路线路线简述

    📜3-甲氧基苯乙酮置于n-溴代丁二酰亚胺(Nbs),对甲苯磺酸体系中,用 乙腈 作为反应溶剂,化学反应 3.0H,以69%的收率获得产物2-溴-3'-甲氧基苯乙酮
    参考文献:通过c(sp3)-O键裂解进行钯催化的α-酰氧基酮的脱羧炔化反应
    标题:通过c(sp3)-O键裂解进行钯催化的α-酰氧基酮的脱羧炔化反应
    摘要:公开了由c(sp 3)-O键断裂引发的钯催化的α-酰氧基酮的脱羧烷基化反应.具有中性反应条件的脱羧策略可以使酮烯醇酸酯发生前所未有的催化炔基化反应.该反应被应用于多种底物,以高收率得到期望的产物.我们成功地通过[pd(cod)(ch 2 Tms)2]与xphos和α-酰氧基酮在室温下的反应合成了一种新的钯-烯酸酯中间体的x射线晶体学,表明c(sp 3)很容易−o键断开.
    DOI:10.1002/chem.201900582

    海关参考信息

    专利信息


    专利号:WO-2021038581-A1
    优先权日:2019-08-30
    标题 :A one step synthesis of 2-substituted benzo[b]thiophenes
    发明人:SEKAR GOVINDASAMY; POONGUZHALI ELAMVAZHUTHI
    权利人:INDIAN INST TECH MADRAS
    摘要:The invention pertains to a one step synthesis of 2-substituted benzo[ b ]thiophene of general formula wherein the synthesis of 2-substituted benzo[ b ]thiophenes is by reacting the starting materials substituted or unsubstituted 2-halogenobenzaldehyde and substituted or unsubstituted acetyl/phenacyl bromide with a catalyst, a sulphur source and phase transfer catalyst in an aqueous medium with atmospheric air and at temperature in the range of 25°C-30°C.

    专利号:US-8178672-B2
    优先权日:2004-10-19
    标 题:Synthesis of imidazooxazole and imidazothiazole inhibitors of p38 MAP kinase
    发明人:ASHWELL MARK A; TANDON MANISH; LAPIERRE JEAN-MARC
    权利人:ASHWELL MARK A; TANDON MANISH; LAPIERRE JEAN-MARC; ARQULE INC
    摘要:An efficient route for the synthesis is of formula (I) of imidazooxazole and imidazothiazole inhibitors of the p38 MAP kinase pathway, useful as therapeutics for disease conditions including inflammation and auto-immune responses is described.

    专利号:US-3714195-A
    优先权日:1970-06-17
    标 题:Ethylenedioxy derivatives of substituted naphthalenone compounds
    发明人:MARINUS L
    权利人:AMERICAN CYANAMID CO
    摘要:This invention relates to substituted naphthalen compounds and their use in the synthesis of D-homosteroids. The latter compounds are useful as estrogenic agents in the treatment of laboratory and domestic animals.

    专利号:US-3806546-A
    优先权日:1969-06-18
    标题 :Steroid-like compounds and method of synthesis
    发明人:LOS M
    权利人:AMERICAN CYANAMID CO
    摘要:THIS INVENTION RELATES TO NOVEL STEROID-LIKE COMPOUNDS, A METHOD FOR THE SYNTHESIS THEREOF AS INTERMEDIATES FOR PREPARING OTHER STEROIDS AND FOR USE OF SUCH COMPOUNDS AS ESTROGENIC, ANDROGENIC OR ANTIOVULATORY AGENTS IN THE TREATMENT OF DOMESTIC AND LABORATORY ANIMALS.

    专利号:US-3736345-A
    优先权日:1971-05-18
    标题 :Steroid-like compounds and method of synthesis
    发明人:LOS M
    权利人:AMERICAN CYANAMID CO
    摘要:THIS INVENTION RELATES TO NOVEL STEROID-LIKE COMPOUNFS, A METHOD FOR THE SYNTHESIS THEREOF AS INTERMEDIATES FOR PREPARING OTHER STEROIDS AND FOR THE USE OF SUCH COMPOUNDS AS ESTROGENIC, ANDROGENIC OR ANTIOVULATORY AGENTS IN THE TREATMENT OF DOMESTIC AND LABORATORY ANIMALS.

    专利号:US-2009111985-A1
    优先权日:2004-10-19
    标 题 :Synthesis of imidazooxazole and imidazothiazole inhibitors of p38 map kinase

    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

    [参考文献]: H Zhang, Et Al. Cyp-Independent Inhibition Of Platelet Aggregation In Rabbits By A Mixed Disulfide Conjugate Of Clopidogrel. Thromb Haemost. 2014 Dec;112(6):1304-11.
    [参考文献]: K E Kristensen, Et Al. Clopidogrel Bioactivation And Risk Of Bleeding In Patients Cotreated With Angiotensin-Converting Enzyme Inhibitors After Myocardial Infarction: A Proof-Of-Concept Study. Clin Pharmacol Ther. 2014 Dec;96(6):713-22.
    [参考文献]: Makoto Takahashi, Et Al. Quantitative Determination Of Clopidogrel Active Metabolite In Human Plasma By Lc-Ms/ms. J Pharm Biomed Anal. 2008 Dec 1;48(4):1219-24.
    [参考文献]: Marta Karaniewicz-Ada, Et Al. The Influence Of Genetic Polymorphism Of Cyp2C19 Isoenzyme On The Pharmacokinetics Of Clopidogrel And Its Metabolites In Patients With Cardiovascular Diseases. J Clin Pharmacol. 2014 Aug;54(8):874-80.
    [参考文献]: Miho Kazui, Et Al. Hepatic Microsomal Thiol Methyltransferase Is Involved In Stereoselective Methylation Of Pharmacologically Active Metabolite Of Prasugrel. Drug Metab Dispos. 2014 Jul;42(7):1138-45.

    合成参考文献


    摘要:Ayad, T.; Pirat, J.-L.; Virieux, D., Science of Synthesis Knowledge Updates, (2022) 1, 343.
    摘要:Amii, H., Science of Synthesis: Modern Strategies in Organofluorine Chemistry, (2025) 2.
    参考文献:10.1107/s1600536810031673
    摘要:Gul S, Siddiqui HL, Ahmad M, Nisar M, Parvez M. 4-Hy-droxy-3-(3-meth-oxybenzoyl)-2-[(3-meth-oxybenzoyl)methyl]-2H-1,2-benzothia-zine 1,1-dioxide. Acta Crystallogr Sect E Struct Rep Online. 2010 Aug 18;66(Pt 9):o2314–5.
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