CAS: 69038-81-9; 3-(2-Ethoxyphenyl)Acrylic Acid

该化合物是一种有机化合物,其特点是其丙基酸结构,其特点是丙烯链第二和第三碳原子之间有双重联系,该化合物含有一个附属于一个苯基环的乙氧组,有助于其独特的化学特性.该化合物一般是一种无色的黄色液体或固体,取决于其纯度和形态.乙氧组的存在会增加其在有机溶剂中的溶性,而氨基酸功能组则具有酸性.该化合物可能展示生物活动,使其在制药和农用化学研究中引起兴趣.该化合物的再活动受到同质双联的影响,允许与核糖化合物发生可能的聚合或反应.与许多有机化合物一样,在处理时应采取安全防范措施,因为如果浸入或浸入,可能会对健康造成危害.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号141-82-2 丙二酸 | CAS号613-69-4 2-乙氧基苯甲醛 | CAS号64-19-7 冰醋酸 | CAS号110-86-1 吡啶 | CAS号599151-35-6 FQI1

合成工艺路线路线简述

  • 合成目标产物 2-Ethoxycinnamic Acid 主要起始原料 Malonic Acid And 2-Ethoxybenzaldehyde
  • (文献来源)合成步骤主要原料 Malonic Acid 和 2-Ethoxybenzaldehyde
📜丙二酸,2-乙氧基苯甲醛置于哌啶体系中,用 吡啶 作为反应溶剂,化学反应 6.0H,反应生成 2-乙氧基肉桂酸
参考文献:通过靶向释放cgrp释放的双靶向rutaecarpine-No供体杂种作为新型抗高血压药
标题:通过靶向释放cgrp释放的双靶向rutaecarpine-No供体杂种作为新型抗高血压药
摘要:Cgrp被认为是最有效的血管扩张药,在高血压的发生和发展中起着重要的作用.trpv1和trpa1在促进cgrp的合成和释放,从而调节心血管张力方面至关重要.rutaecarpine通过刺激cgrp合成和通过激活trpv1释放而表现出有效的血管舒张和高血压作用.并且已经显示no在体内与h 2 S反应形成hno,从而激活hno-Trpa1-Cgrp途径.受联合疗法的启发,设计,合成和评估了11种芸香果树素-呋喃聚糖杂种.结果表明,大多数杂种发挥相当或改善的血管扩张活性.其中13A是离体细胞(ec)最有效的50 = 13.1 Nm)和体内.机理研究表明,杂种的血管舒张作用和抗高血压作用可能涉及通过trpv1和trpa1的双重激活促进cgrp释放.这项工作表明,双靶杂种可能是发现和开发新型抗高血压药物的有效且有前途的方法.
DOI:10.1016/j.Ejmech.2019.02.037

海关参考信息

专利信息


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: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.

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

参考标题:Design And Synthesis Of Novel 2-Phenylaminopyrimidine (Pap) Derivatives And Their Antiproliferative Effects In Human Chronic Myeloid Leukemia Cells
作者:Sheng Chang,Shi-Liang Yin,Jian Wang,Yong-Kui Jing,Jin-Hua Dong
摘要:A Series Of Novel 2-Phenylaminopyrimidine (Pap) Derivatives Structurally Related To Sti-571 Were Designed And Synthesized. The Abilities Of These Compounds To Inhibit Proliferation Were Tested In Human Chronic Myeloid Leukemia K562 Cells. (E)-3-(2-Bromophenyl)-N-[4-Methyl-3-(4-Pyridin-3-Yl-Pyrimidin-2-Ylamino)Phenyl]Acrylamide(12D) Was The Most Effective Cell Growth Inhibitor And Was 3-Fold More Potent Than Sti-571.

合成参考文献


参考文献:10.1107/s0108768104009048
摘要:Fernandes MA, Levendis DC, Schoening FRL. A new polymorph of ortho-ethoxy-trans-cinnamic acid: single-to-single-crystal phase transformation and mechanism. Acta Crystallogr B Struct Sci. 2004 May 17;60(3):300–14. doi: 10.1107/s0108768104009048.
参考文献:10.1107/s0108768104007955
摘要:Fernandes MA, Levendis DC. Photodimerization of the α′-polymorph of ortho-ethoxy-trans-cinnamic acid in the solid state. I. Monitoring the reaction at 293 K. Acta Crystallogr B Struct Sci. 2004 May 17;60(3):315–24. doi: 10.1107/s0108768104007955.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知