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(Z)-methyl 3-phenyl-3-phenylthiopropenoate | 34875-03-1

中文名称
——
中文别名
——
英文名称
(Z)-methyl 3-phenyl-3-phenylthiopropenoate
英文别名
(Z)-methyl 3-phenyl-3-(phenylthio)acrylate;methyl (Z)-3-phenylthiocinnamate;trans-β-Phenylthio-zimtsaeuremethylester;methyl (Z)-3-phenyl-3-phenylsulfanylprop-2-enoate
(Z)-methyl 3-phenyl-3-phenylthiopropenoate化学式
CAS
34875-03-1
化学式
C16H14O2S
mdl
——
分子量
270.352
InChiKey
YGTAIVSANUZYGZ-QINSGFPZSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    19
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Copper-Catalyzed Synthesis of Vinyl Sulfides
    作者:Craig G. Bates、Pranorm Saejueng、Michael Q. Doherty、D. Venkataraman
    DOI:10.1021/ol0477935
    日期:2004.12.1
    [reaction: see text] We report a method for the synthesis of vinyl sulfides using the soluble copper(I) catalyst [Cu(phen)(PPh3)2]NO3. The desired vinyl sulfides are obtained in good to excellent yields, with retention of stereochemistry. This protocol tolerates a wide variety of functional groups or substrates, is palladium-free, and does not require the use of expensive or air-sensitive additives
    [反应:见正文]我们报告了一种使用可溶性铜(I)催化剂[Cu(phen)(PPh3)2] NO3合成乙烯基硫化物的方法。以良好至优异的产率获得所需的乙烯基硫化物,并保留了立体化学。该方案可耐受多种官能团或底物,不含钯,并且不需要使用昂贵或对空气敏感的添加剂。
  • Hamed, Ezzat A., Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical, 1997, vol. 36, # 1, p. 102 - 104
    作者:Hamed, Ezzat A.
    DOI:——
    日期:——
  • Substitution and elimination reactions in chloro olefins. 3. Reactions of methyl .beta.-chlorocinnamates with thiophenoxide ion
    作者:Abdel-Hamid A. Youssef、Saber M. Sharaf、Samir K. El-Sadany、Ezzat A. Hamad
    DOI:10.1021/jo00332a010
    日期:1981.9
  • The first synthesis of β-phenylchalcogeno-α,β-unsaturated esters via hydrochalcogenation of acetylenes using microwave and solvent-free conditions
    作者:Gelson Perin、Raquel G. Jacob、Francisco de Azambuja、Giancarlo V. Botteselle、Geonir M. Siqueira、Rogério A. Freitag、Eder J. Lenardão
    DOI:10.1016/j.tetlet.2005.01.060
    日期:2005.3
    A simple, clean, and efficient solvent-free protocol was developed for hydrochalcogenation of methyl propiolate derivatives with phenylchalcogenolate anion generated in situ from the respective diphenyl dichalcogenide (S, Se, Te) using alumina supported sodium borohydride. This efficient and improved method is general and furnishes the (Z)-beta-phenylchalcogeno-alpha,beta-unsaturated esters in yields and with selectivity comparable to those using organic solvent and inert atmosphere. The use of MW irradiation facilitates the procedure and accelerates the reaction. (C) 2005 Elsevier Ltd. All rights reserved.
  • BHONGLE, N. N.;GOGTE, V. N.;VANKAR, Y. D., INDIAN J. CHEM., 1982, 21, N 8, 724-728
    作者:BHONGLE, N. N.、GOGTE, V. N.、VANKAR, Y. D.
    DOI:——
    日期:——
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