CAS: 539-47-9; 3-(Furan-2-yl)Acrylic Acid

该化合物是一种以松动的不饱和碳酸,配有分子式C7H6O3.这种化合物具有呋喃环和丙烯酸酸混合物之间的共聚系统,使它成为有机合成的多功能中间体.它的α,β-不饱和碳基结构允许参与Michael添加,Diels-Alder反应和其他同源添加过程.这种纤维基组增强了其在热循环化学中的效用,特别是在生物活性分子和功能材料合成方面的效用.这种化合物一般在室温下是固体的,在极有机溶剂中表现出中等溶性.其定义明确的再活动特征使得它对于制药和农用化学研究很有价值.

结构式图片

相似化合物

623-30-3 39511-08-5 15690-24-1

欧盟法规

ECHA物质C&L通报REACH预注册

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合成工艺路线路线简述

    2-呋喃丙烯醛置于palladium(II) Trifluoroacetate,双氧水体系中,用 N,N-二甲基乙酰胺,水 作为反应溶剂,化学反应 0.17H,以53%的收率获得产物2-呋喃丙烯酸
    参考文献:钯 (II) 催化的 α,β-不饱和醛与过氧化氢选择性氧化为 α,β-不饱和羧酸
    标题:钯 (II) 催化的 α,β-不饱和醛与过氧化氢选择性氧化为 α,β-不饱和羧酸
    摘要:进行钯 (II) 催化的 α,β-不饱和醛与过氧化氢的化学选择性氧化,得到 α,β-不饱和羧酸.肉桂醛被有效催化...
    DOI:10.1246/cl.2009.430

    海关参考信息

    专利信息


    专利号:US-4910330-A
    优先权日:1987-09-25
    标题 :Synthesis of sulfonic acids and carboxylic acid ester derivatives thereof
    发明人:MCGEE DENNIS E; HALLEN TED S
    权利人:UNION OIL CO
    摘要:Hydroxy sulfonic acids in general and isethionic acid (2-hydroxy ethyl sulfonic acid) in particular can be prepared at 99+% purity and good yields by the selective oxidation of a precursor hydroxy mercaptan with hydrogen peroxide. The resulting product is pure enough to be used directly in the synthesis of sulfo-acrylic esters which are finding considerable use as stabilizers in producing vinylidene chloride copolymers used for FDA approved packaging films.

    专利号:US-4987250-A
    优先权日:1987-09-25
    标 题:Synthesis of hydroxy sulfonic acids
    发明人:MCGEE DENNIS E; HALLEN TED S
    权利人:UNION OIL CO
    摘要:Hydroxy sulfonic acids in general and isethionic acid (2-hydroxy ethyl sulfonic acid) in particular can be prepared at 99+% purity and good yields by the selective oxidation of a precursor hydroxy mercaptan with hydrogen peroxide. The resulting product is pure enough to be used directly in the synthesis of sulfo-acrylic esters which are finding considerable use as stabilizers in producing vinylidene chloride copolymers used for FDA approved packaging films.

    专利号:US-8951728-B2
    优先权日:2004-11-22
    标 题:Template directed split and mix synthesis of small molecule libraries
    发明人:RASMUSSEN PETER BIRK
    权利人:CHEMGENE HOLDING APS
    摘要:The invention combines the advantages of split and mix synthesis with the advantages of template directed synthesis. The method comprises the steps of: a) adding a linker molecule L to one or more reaction wells; b) adding a molecule fragment to each of said reaction wells; c) adding an oligonucleotide identifier to each of said reaction wells; d) subjecting said wells to conditions sufficient to allow said molecule fragments and said oligonucleotide identifiers to become attached to said linker molecule, or conditions sufficient for said molecule fragments to bind to other molecule fragments and sufficient for said oligonucleotide identifiers to bind to other oligonucleotide identifiers; e) combining the contents of said one or more reaction wells; and f) contacting the resulting bifunctional molecule(s) of step e) with one or more (oligonucleotide) templates each capable of hybridizing to at least one of the oligonucleotide identifiers added in step c).

    专利号:US-7109377-B2
    优先权日:1996-10-16
    标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
    发明人:SCHREIBER STUART L; SHAIR MATTHEW D; TAN DEREK S; FOLEY MICHAEL A; STOCKWELL BRENT R
    权利人:HARVARD COLLEGE
    摘要:The present invention provides complex compounds reminiscent of natural products and libraries thereof, as well as methods for their production. The inventive compounds and libraries of compounds are reminiscent of natural products in that they contain one or more stereocenters, and a high density and diversity of functionality. In general, the inventive libraries are synthesized from diversifiable scaffold structures, which are synthesized from readily available or easily synthesizable template structures. In certain embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from a shikimic acid based epoxyol template. In other embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from the pyridine-based template isonicotinamide. The present invention also provides a novel ortho-nitrobenzyl photolinker and a method for its synthesis. Furthermore, the present invention provides methods and kits for determining one or more biological activities of members of the inventive libraries. Additionally, the present invention provides pharmaceutical compositions containing one or more library members.

    专利号:WO-2012152438-A1
    优先权日:2011-05-11
    标题 :Process for the preparation of nitrate acid ester of organic compounds
    发明人:BONFANTI ANNALISA; STORONI LAURA; RONSIN GAEL
    权利人:NICOX SA; BONFANTI ANNALISA; STORONI LAURA; RONSIN GAEL
    摘要:The present invention relates to a one-step process for the synthesis of nitric acid esters or 15 N isotopically labeled nitrate esters of organic compounds starting from the correspondent alcohols. Formula (I).

    专利号:US-11225655-B2
    优先权日:2010-04-16
    标题:Bi-functional complexes and methods for making and using such complexes
    发明人:GOULIAEV ALEX HAAHR; FRANCH THOMAS; GODSKESEN MICHAEL ANDERS; JENSEN KIM BIRKEBAEK
    权利人:GOULIAEV ALEX HAAHR; FRANCH THOMAS; GODSKESEN MICHAEL ANDERS; JENSEN KIM BIRKEBAEK; NUEVOLUTION AS
    摘要:The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: P Bünning, Et Al. Activation Of Angiotensin Converting Enzyme By Monovalent Anions. Biochemistry. 1983 Jan 4;22(1):110-6.
    [参考文献]: P Bünning, Et Al. Substrate Specificity And Kinetic Characteristics Of Angiotensin Converting Enzyme. Biochemistry. 1983 Jan 4;22(1):103-10.

    合成参考文献


    参考文献:10.1007/s10593-023-03250-7
    摘要:Kalyaev MV, Ryabukhin DS, Ivanov AY, Boyarskaya IA, Borovkova KE, Nikiforova LR, Salmova JV, Taraskin AO, Puzyk AM, Vasilyev AV. Hydroarylation of carbon–carbon double bond of furanic conjugated enones by arenes under superelectrophilic activation: synthesis and evaluation of antimicrobial activity of novel furan derivatives. Chem Heterocycl Comp. 2023 Sep;59(9-10):646–56. doi: 10.1007/s10593-023-03250-7.
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