CAS: 33538-83-9; 3-(2-Methoxyphenyl)Propanal

该化合物是具有甲状腺功能组和甲氧代代苯环特征的有机化合物;该化合物具有一种丙烷基脊,由三碳链组成,在甲酰基组(CHO)中终止;2甲基苯基组的存在具有芳香特性,影响化合物的再活性和溶性.一般而言,此类化合物具有中度极性,其原因是有氢恐惧芳香环和水氧代苯基合金组的结合.这一结构可导致有趣的化学行为,包括在典型的甲醚的核细胞添加反应中的潜在再活动.此外,甲氧基组可以参与各种相互作用,如氢结合和二极相互作用,影响该化合物的物理特性,如不同溶剂中的沸点和溶性等.总体而言,3-(2-乙氧基苯基)异丙胺体对有机合成感兴趣,并可能用于制药或作为化学品制造的中间体.

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CAS号5720-06-9 2-甲氧基苯基硼酸 | CAS号107-18-6 烯丙醇 | CAS号79-37-8 草酰氯 | CAS号10493-37-5 邻甲氧基苯丙醇 | CAS号529-28-2 邻碘苯甲醚 | CAS号201230-82-2 carbon monoxide | CAS号612-15-7 2-甲氧基苯乙烯 | CAS号6099-03-2 2-甲氧基肉桂酸 | CAS号1504-61-6 o-Methoxycinnam... | CAS号1504-74-1 邻甲氧基肉桂醛 | CAS号1504-74-1 邻甲氧基肉桂醛 | CAS号60125-24-8 3-(2-甲氧基苯基)-2-丙烯醛

合成工艺路线路线简述

  • 合成目标产物 3-(2-Methoxy-Phenyl)-Propionaldehyde 主要起始原料 2'-Methoxycinnamaldehyde
  • (文献来源)合成步骤主要原料 2'-Methoxycinnamaldehyde
📜2-甲氧基肉桂酸置于lithium Aluminium Tetrahydride,Pyridinium Chlorochromate体系中,用 四氢呋喃,二氯甲烷 用作溶剂,化学反应生成3-(2-甲氧基-苯基)-丙醛
参考文献:Synthesis Of 2-Tetralone Derivatives By Bi(Otf)3-Catalyzed Intramolecular Hydroarylation/isomerization Of Propargyl Alcohols
标题:Synthesis Of 2-Tetralone Derivatives By Bi(Otf)3-Catalyzed Intramolecular Hydroarylation/isomerization Of Propargyl Alcohols
摘要:Compared To 1-Tetralones,2-Tetralones Are Expensive,Less Stable,And Difficult To Synthesize. A Concise Bi-Catalyzed Method Was Developed For The Synthesis Of 2-Tetralones From 5-Phenylpent-1-Yn-3-Ol Derivatives. Diverse 2-Tetralones Were Obtained In Moderate To Good Yields Under Mild Conditions. (C) 2015 Elsevier Ltd. All Rights Reserved.
Doi:10.1016/j.Tetlet.2014.12.129

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专利信息


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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合成参考文献


摘要:Hamel, J.-D.; Paquin, J.-F., Science of Synthesis Knowledge Updates, (2016) 1, 414.
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