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ethyl 3-(2,5-dimethyl-1H-pyrrol-3-yl)cinnamate | 628314-44-3

中文名称
——
中文别名
——
英文名称
ethyl 3-(2,5-dimethyl-1H-pyrrol-3-yl)cinnamate
英文别名
ethyl (Z)-3-(2,5-dimethyl-1H-pyrrol-3-yl)-3-phenylprop-2-enoate
ethyl 3-(2,5-dimethyl-1H-pyrrol-3-yl)cinnamate化学式
CAS
628314-44-3
化学式
C17H19NO2
mdl
——
分子量
269.343
InChiKey
IZZQRVGUJVMBNW-WJDWOHSUSA-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
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    42.1
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2,5-二甲基吡咯苯丙炔酸乙酯potassium tetrachloroplatinatesilver trifluoromethanesulfonate 作用下, 以 溶剂黄146 为溶剂, 反应 24.0h, 生成 ethyl 3-(2,5-dimethyl-1H-pyrrol-3-yl)cinnamate 、 ethyl 3-(2,5-dimethyl-1H-pyrrol-3-yl)cinnamate
    参考文献:
    名称:
    Pt(II)-catalyzed hydroarylation reaction of alkynes with pyrroles and furans
    摘要:
    A Pt(II) catalyst showed a drastic effect on hydroarylation of alkynes with pyrroles and furans compared with Pd(OAc)(2) catalyst. The hydroarylation reactions proceeded smoothly under mild conditions to double-hydroarylation products in good yields. Mono-adducts Were formed only when the second hydroarylation was inhibited by steric hindrance Of Substrates or low reactivity of the mono-adducts. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.03.022
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文献信息

  • Pt(II)-catalyzed hydroarylation reaction of alkynes with pyrroles and furans
    作者:Juzo Oyamada、Tsugio Kitamura
    DOI:10.1016/j.tet.2009.03.022
    日期:2009.5
    A Pt(II) catalyst showed a drastic effect on hydroarylation of alkynes with pyrroles and furans compared with Pd(OAc)(2) catalyst. The hydroarylation reactions proceeded smoothly under mild conditions to double-hydroarylation products in good yields. Mono-adducts Were formed only when the second hydroarylation was inhibited by steric hindrance Of Substrates or low reactivity of the mono-adducts. (C) 2009 Elsevier Ltd. All rights reserved.
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