CAS: 1011-92-3; 2-Cyano-3-Phenylacrylic Acid

该化合物是一种多用途有机化合物,其特点是与苯代基替代丙基骨相连的丙基基酸和箱状酸功能组,这种结构使其成为有机合成中有价值的中间体,特别是用于建造异环循环和同质系统,其用电拖式的西诺组增强了迈克尔添加和循环反应的再活性,而箱状酸混合物允许进一步衍生.该化合物通常用于制药和农用化学研究,因为它能够作为生物活性分子的前体,在标准条件下保持稳定,而且与各种反应条件相容,进一步有助于其在合成化学中的用途.

结构式图片

相似化合物

2700-22-3 148238-25-9 584-45-2

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上下游产品

CAS号100-52-7 苯甲醛 | CAS号372-09-8 氰基乙酸 | CAS号105-56-6 氰乙酸乙酯 | CAS号4360-49-0 α-Hydroxymethyl... | CAS号139413-81-3 2-(bromomethyl)... | CAS号120-92-3 环戊酮 | CAS号96-15-1 2-甲基丁胺 | CAS号593-51-1 一甲胺盐酸盐 | CAS号142-04-1 苯胺盐酸盐 | CAS号3695-84-9 2-氰基-3-苯基丙烯酸甲酯 | CAS号141-82-2 丙二酸 | CAS号7664-41-7 氨 | CAS号100-52-7 苯甲醛 | CAS号4360-47-8 3-苯基丙烯腈 | CAS号124-38-9 二氧化碳 | CAS号635-51-8 苯基丁二酸 | CAS号5331-42-0 2-氰基-3-苯基丙酸 | CAS号102-93-2 3-苯基丙酰胺 | CAS号372-09-8 氰基乙酸

合成工艺路线路线简述

  • 合成目标产物 Alpha-Cyanocinnamic Acid 主要起始原料 Benzyl Alcohol
  • (文献来源)合成步骤主要原料 Benzyl Alcohol
📜苯甲醇置于哌啶,Sodium Hypochlorite,2,2,6,6-四甲基哌啶氧化物,碳酸氢钠,Potassium Bromide体系中,用 二氯甲烷,水 用作溶剂,100.0 °C,600.01 Kpa 条件下,反应 1.21H,反应生成α-氰基肉桂酸
参考文献:化学组装系统:活性药物成分的分散,连续,多步合成的分层控制
标题:化学组装系统:活性药物成分的分散,连续,多步合成的分层控制
摘要:尽管连续化学过程吸引了学术界和工业界的兴趣,但实际上所有活性药物成分(api)仍是通过使用多个不同的批处理过程来生产的.迄今为止,还没有用于可定制的小分子的不同的多步连续生产的方法.开发了一种化学装配系统,该系统中的流动反应模块以可互换的方式链接在一起,从而可以访问广泛的化学空间.在三个不同级别上进行控制-原料,试剂或反应模块的顺序选择-可以合成代表三个不同结构类别(γ-氨基酸,γ-内酰胺,β-氨基酸)的五个api,包括大片药物lyrica和gabapentin,总收率非常好(49-75%).
Doi:10.1002/anie.201409765

海关参考信息

  • 2905121000-正丙醇
    2905290000-其他不饱和一元醇
    2905399099-其他二元醇
    2905499000-其他多元醇
    2905590090-其他无环醇的卤化、磺化等衍生物
  • 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
  • 详情请参考:📖 海关编码查询和海关进出口税则

专利信息


专利号:US-4567265-A
优先权日:1984-01-16
标题:Cyclopropanoid cyanoesters and method of making same
发明人:BABLER JAMES H
权利人:UNIV LOYOLA CHICAGO
摘要:Cyclopropanoid cyanoesters of the formula: where R' is -CH3 or -CH2CH3, and A is (a) -H, or (b) A, B represents an aliphatic group joined to a carbon atom on the cyclopropanoid ring, thereby forming a spiro group, A, B being selected from structures having the formula: (i) -(CH2)n-, wherein n=3, 4, or 5, and (ii) -(CH2)2-Y-(CH2)2-, wherein Y is NCH3, O, or S); and, when A is -H, B is selected from the group consisting of: +TR (CH3)2CHCH2. are disclosed. These compositions are useful in the synthesis of pyrethroids. A process for synthesis of cyclopropanoid cyanoesters by reacting 2-nitropropane with cyanoesters of the general formula: is also disclosed and claimed.

专利号:US-6531470-B1
优先权日:1998-01-23
标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
权利人:UPJOHN CO
摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

专利号:CN-113149865-B
优先权日:2021-04-07
标题 :Preparation method and application of organic basic catalyst for catalytic synthesis of alpha-cyano ethyl cinnamate

专利号:US-6562844-B2
优先权日:1998-01-23
标 题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
权利人:UPJOHN CO
摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

专利号:US-7002020-B1
优先权日:1998-01-23
标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V
权利人:UPJOHN CO
摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

专利号:US-2023103693-A1
优先权日:2019-12-20
标 题 :Synthesis of compounds to promote hair growth

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📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

合成参考文献


摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 210.
摘要:National Academy of Sciences, National Research Council, Chemical-Biological Coordination Center, Review., 5(7), 1953
参考文献:10.1002/hipo.22958
摘要:Herrera-López G, Galván EJ. Modulation of hippocampal excitability via the hydroxycarboxylic acid receptor 1. Hippocampus. 2018 Aug;28(8):557–67. doi: 10.1002/hipo.22958.
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