CAS: 19757-97-2; Methyl 2-Hydroxy-2-Methoxyacetate

该化合物是一种有机化合物,其特点是其酯类功能组;其特征为一种甲基氧基(-OCH3)和一种与碳原子中枢相连的氢氧基(-OH)组,其作用性能和溶解性能有一定的特性;该化合物一般是无色的,可粉色黄色,具有舒适的味道,适合用于各种用途,包括溶剂或其他有机化合物的合成;其分子结构允许氢结合,从而增强其在极地溶剂中的溶性. 甲基2-羟氧-2-甲基氧基乙酸酯在制药和农用化学品生产中的潜在用途也众所周知,因为它的功能组群可以参与进一步的化学反应.安全数据表明,与许多有机溶剂一样,应谨慎地处理,因为吸入或摄入后可能构成健康风险.适当的储存和处理程序对于确保实验室和工业环境中的安全至关重要.

结构式图片

相似化合物

563-96-2 73569-40-1 18370-95-1

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

furfural methanol Glyoxilic acid GlyoxalMethyl dimethoxyacetate methyl 2-(tert-butoxycarbonylamino)-2-hydroxyacetate (2R,4aS,7R,8aR)-3-Benzyl-4,4,7-trimethyl-°Ctahydro-benzo[e][1,3]oxazine-2-carboxylic acid methyl ester -°Ctahydro-3-(phenylmethyl)-4,4,7-trimethyl-2H-1,3-benzooxazine-2-carboxylatemethyl 2S(2α,4aα,7α,8aβ)-°Ctahydro-3-(phenylmethyl)-4,4,7-trimethyl-2H-1,3-benzooxazine-2-carboxylate

合成工艺路线路线简述

    甲酸甲酯置于sodium Hydroxide,Wang Resin-Pentylstyrene[5-Ph(4Me)]N-Me-Imidazole(1+)*cl(1-)体系中,用 四氢呋喃 用作溶剂,化学反应 1.5H,以41%的收率获得2-羟基-2-甲氧基乙酸甲酯
    参考文献:Imidazole Based Solid-Supported Catalysts For The Benzoin Condensation
    标题:Imidazole Based Solid-Supported Catalysts For The Benzoin Condensation
    摘要:New Polymer-Supported Imidazolium Salts Have Been Synthesised,And Their Utility As Pre-Catalysts In The Benzoin Reaction Has Been Demonstrated. (C) 2005 Elsevier Ltd. All Rights Reserved.
    Doi:10.1016/j.Tetlet.2005.08.141

    海关参考信息

    专利信息


    专利号:US-9969685-B2
    优先权日:2016-09-28
    标 题 :Enantioselective synthesis of pyrroloindole compounds
    发明人:SCHMIDT MICHAEL ANTHONY
    权利人:BRISTOL MYERS SQUIBB CO
    摘要:Compounds according to formula (I) or (II), wherein R 1 , R 2 , and R 3 are as defined in the specification, are versatile intermediates for the synthesis of DNA minor groove binder-alkylators having a cyclopropapyrroloindole (CPI) or seco-CPI alkylating subunit.

    专利号:US-4424389-A
    优先权日:1981-04-30
    标 题:Synthesis of 6-hydroxychroman-2-methanol derivatives
    发明人:SAKITO YOJI
    权利人:SUMITOMO CHEMICAL CO
    摘要:A process for producing chroman, a compound of the formula, ##STR1## or an optically active compound thereof wherein R 2 , R 3 and R 4 are each a hydrogen atom or a C 1 -C 4 alkyl group, which comprises reacting a compound of the formula, ##STR2## or an optically active compound thereof wherein A is an aryl group and R 5 is a C 1 -C 4 alkyl group, with a compound of the formula, ##STR3## wherein R 1 is a C 1 -C 3 alkyl group, X is a halogen atom and R 2 , R 3 and R 4 are as defined above, to obtain a compound of the formula, ##STR4## or an optically active compound thereof wherein A, R 1 , R 2 , R 3 and R 4 are as defined above, reacting the resulting compound with methylmagnesium halide and then hydrolyzing to obtain the corresponding 4-aryl substituted 2-hydroxy-2-methylbutanal, or an optically active compound thereof, reducing the resulting compound to obtain a diol, or an optically active compound thereof, and then oxidizing the resulting compound to obtain a compound of the formula, ##STR5## or an optically active compound thereof wherein R 2 , R 3 and R 4 are as defined above, followed by reduction. n Chromans, the objective compounds of this invention, are an intermediate for the synthesis of tocopherols, particularly α-tocopherol.

    专利号:US-8324417-B2
    优先权日:2009-08-19
    标题:Process for the preparation of (S)-2-amino-5-cyclopropyl-4,4-difluoropentanoic acid and alkyl esters and acid salts thereof
    发明人:HART BARRY; DENER JEFF; GREEN MICHAEL; STANDEN MICHAEL; KOCIAN OLDRICH
    权利人:HART BARRY; DENER JEFF; GREEN MICHAEL; STANDEN MICHAEL; KOCIAN OLDRICH; VIROBAY INC
    摘要:The present invention relates to a process for the preparation of alkyl esters of (S)-2-amino-5-cyclopropyl-4,4-difluoropentanoic acid, which are intermediates useful in the synthesis of (S)—N-(1-cyanocyclopropyl)-5-cyclopropyl-4,4-difluoro-2-((S)-2,2,2-trifluoro-1-(4-fluorophenyl)ethylamino)pentanamide and related compounds, which are compounds that are cysteine protease inhibitors.

    专利号:US-9718807-B2
    优先权日:2012-06-05
    标 题 :Synthesis of antiviral compound
    发明人:SCOTT ROBERT WILLIAM; VITALE JUSTIN PHILIP; MATTHEWS KENNETH STANLEY; TERESK MARTIN GERALD; FORMELLA ALEXANDRA; EVANS JARED WAYNE
    权利人:GILEAD PHARMASSET LLC
    摘要:The present disclosure provides processes for the preparation of a compound of formula I: n nwhich is useful as an antiviral agent. The disclosure also provides compounds that are synthetic intermediates to compounds of formula I.

    专利号:US-7205300-B2
    优先权日:1997-12-31
    标 题:Aryl fused azapolycyclic compounds
    发明人:COE JOTHAM WADSWORTH; BROOKS PAIGE ROANNE PALMER
    权利人:PFIZER
    摘要:This invention is directed to compounds of the formula (I): n nand their pharmaceutically acceptable salts, wherein R 1 , R 2 , and R 3 are as defined herein; intermediates for the synthesis of such compounds, pharmaceutical compositions containing such compounds; and methods of using such compounds in the treatment of neurological and psychological disorders.

    专利号:WO-2018064094-A1
    优先权日:2016-09-28
    标题:Enantioselective synthesis of pyrroloindole compounds
    杭州凯邦生物科技有限公司
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    主要参考文献

    参考标题:Total Synthesis Of The Serine-Threonine Phosphatase Inhibitor Microcystin-La
    作者:John M. Humphrey,James B. Aggen,A. Richard Chamberlin |发布日期:1996.1.1
    摘要:Element Of The Cell. There Is A Diverse Group Of Toxic Natural Products That Inhibit Certain Phosphatases, Thereby Disrupting Normal Biochemical Pathways. These Toxins Can Be Useful For Dissecting The Individual Biochemical Pathways Associated With Each Of These Enzymes. This Article Describes The First Total Synthesis Of One Such Toxin, The Cyclic Heptapeptide Microcystin-La. The Synthesis Features A Convergent

    合成参考文献


    摘要:Poechlauer, P.; Zimmermann, A., Science of Synthesis: Catalytic Reduction in Organic Synthesis, (2017) 1, 331.
    参考文献:10.1038/s41698-020-0121-2
    摘要:Datta P, Dey M, Ataie Z, Unutmaz D, Ozbolat IT. 3D bioprinting for reconstituting the cancer microenvironment. npj Precision Oncology. 2020 Jul 27;4(1):18. doi: 10.1038/s41698-020-0121-2.
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