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ethyl 3-cyclopentyl-5-phenylpentanoate | 1132649-93-4

中文名称
——
中文别名
——
英文名称
ethyl 3-cyclopentyl-5-phenylpentanoate
英文别名
Ethyl 3-cyclopentyl-5-phenylpentanoate
ethyl 3-cyclopentyl-5-phenylpentanoate化学式
CAS
1132649-93-4
化学式
C18H26O2
mdl
——
分子量
274.403
InChiKey
OGOZBDAKFNDXNY-UHFFFAOYSA-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

物化性质

  • 沸点:
    374.4±21.0 °C(predicted)
  • 密度:
    1.012±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    20
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    碘代环戊烷ethyl 5-phenyl-2-pentenoate 在 indium(III) chloride 、 indiumcopper(l) iodide 作用下, 以 为溶剂, 反应 24.0h, 以84%的产率得到ethyl 3-cyclopentyl-5-phenylpentanoate
    参考文献:
    名称:
    Indium/copper-mediated conjugate addition of unactivated alkyl iodides to α,β-unsaturated carbonyl compounds in water
    摘要:
    An efficient method for the conjugate addition of unactivated alkyl iodides to alpha,beta-Unsaturated carbonyl compounds using indium/copper in water is described. The reactions proceed more efficiently in water than in organic solvents. In, CuI, and InCl3 are all essential for efficient reaction. Formation of a symmetrical vic-diarylalkane is observed when an aryl-substituted alkene is used as substrate. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.12.079
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文献信息

  • Indium/copper-mediated conjugate addition of unactivated alkyl iodides to α,β-unsaturated carbonyl compounds in water
    作者:Zhi-Liang Shen、Hao-Lun Cheong、Teck-Peng Loh
    DOI:10.1016/j.tetlet.2008.12.079
    日期:2009.3
    An efficient method for the conjugate addition of unactivated alkyl iodides to alpha,beta-Unsaturated carbonyl compounds using indium/copper in water is described. The reactions proceed more efficiently in water than in organic solvents. In, CuI, and InCl3 are all essential for efficient reaction. Formation of a symmetrical vic-diarylalkane is observed when an aryl-substituted alkene is used as substrate. (C) 2009 Elsevier Ltd. All rights reserved.
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