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ethyl 5-(4-acetylphenoxy)pentanoate | 1343498-44-1

中文名称
——
中文别名
——
英文名称
ethyl 5-(4-acetylphenoxy)pentanoate
英文别名
——
ethyl 5-(4-acetylphenoxy)pentanoate化学式
CAS
1343498-44-1
化学式
C15H20O4
mdl
——
分子量
264.321
InChiKey
GJODJPQGLZLYAV-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.0
  • 重原子数:
    19.0
  • 可旋转键数:
    8.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    52.6
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    ethyl 5-(4-acetylphenoxy)pentanoate 在 potassium hydroxide 、 盐酸 作用下, 以 乙醇 为溶剂, 生成 5-(4-ethanoylphenoxy)pentanoic acid
    参考文献:
    名称:
    Discovery of gemfibrozil analogues that activate PPARα and enhance the expression of gene CPT1A involved in fatty acids catabolism
    摘要:
    A new series of gemfibrozil analogues conjugated with alpha-asarone, trans-stilbene, chalcone, and their bioisosteric modifications were synthesized and evaluated to develop PPAR alpha agonists. In this attempt, we have removed the methyls on the phenyl ring of gemfibrozil and introduced the above scaffolds in para position synthesizing two series of derivatives, keeping the dimethylpentanoic skeleton of gemfibrozil unaltered or demethylated. Four compounds exhibited good activation of the PPAR alpha receptor and were also screened for their activity on PPAR alpha-regulated gene CPT1A. (C) 2011 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2011.08.022
  • 作为产物:
    描述:
    5-溴戊酸乙酯对羟基苯乙酮sodium 作用下, 以 乙醇 为溶剂, 反应 0.5h, 生成 ethyl 5-(4-acetylphenoxy)pentanoate
    参考文献:
    名称:
    Discovery of gemfibrozil analogues that activate PPARα and enhance the expression of gene CPT1A involved in fatty acids catabolism
    摘要:
    A new series of gemfibrozil analogues conjugated with alpha-asarone, trans-stilbene, chalcone, and their bioisosteric modifications were synthesized and evaluated to develop PPAR alpha agonists. In this attempt, we have removed the methyls on the phenyl ring of gemfibrozil and introduced the above scaffolds in para position synthesizing two series of derivatives, keeping the dimethylpentanoic skeleton of gemfibrozil unaltered or demethylated. Four compounds exhibited good activation of the PPAR alpha receptor and were also screened for their activity on PPAR alpha-regulated gene CPT1A. (C) 2011 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2011.08.022
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