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2-(4-(p-tolyl)butyl)propane-1,3-diol | 1089672-22-9

中文名称
——
中文别名
——
英文名称
2-(4-(p-tolyl)butyl)propane-1,3-diol
英文别名
——
2-(4-(p-tolyl)butyl)propane-1,3-diol化学式
CAS
1089672-22-9
化学式
C14H22O2
mdl
——
分子量
222.327
InChiKey
ZUXNNERWBMTFDD-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:
    383.8±37.0 °C(Predicted)
  • 密度:
    1.027±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.31
  • 重原子数:
    16.0
  • 可旋转键数:
    7.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    40.46
  • 氢给体数:
    2.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Discovery of a highly orally bioavailable c-5-[6-(4-Methanesulfonyloxyphenyl)hexyl]-2-methyl-1,3-dioxane-r-2-carboxylic acid as a potent hypoglycemic and hypolipidemic agent
    摘要:
    A series of novel 1,3-dioxane-2-carboxylic acid derivatives containing alkyl chain tether and substituted phenyl group as a lipophilic tail have been prepared as agonists of PPAR alpha and gamma. c-5-[6-(4-Methanesulfonyloxyphenyl) hexyl]-2-methyl-1,3-dioxane-r-2-carboxylic acid 13c exhibited potent hypoglycemic and lipid lowering activity with high oral bioavailability in animal models. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.08.112
  • 作为产物:
    描述:
    Diethyl 2-[4-(4-methylphenyl)butyl]propanedioate 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 生成 2-(4-(p-tolyl)butyl)propane-1,3-diol
    参考文献:
    名称:
    Discovery of a highly orally bioavailable c-5-[6-(4-Methanesulfonyloxyphenyl)hexyl]-2-methyl-1,3-dioxane-r-2-carboxylic acid as a potent hypoglycemic and hypolipidemic agent
    摘要:
    A series of novel 1,3-dioxane-2-carboxylic acid derivatives containing alkyl chain tether and substituted phenyl group as a lipophilic tail have been prepared as agonists of PPAR alpha and gamma. c-5-[6-(4-Methanesulfonyloxyphenyl) hexyl]-2-methyl-1,3-dioxane-r-2-carboxylic acid 13c exhibited potent hypoglycemic and lipid lowering activity with high oral bioavailability in animal models. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.08.112
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