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1-[2-Hydroxy-4-[3-(4-methoxyphenoxy)propoxy]phenyl]ethanone | 63360-03-2

中文名称
——
中文别名
——
英文名称
1-[2-Hydroxy-4-[3-(4-methoxyphenoxy)propoxy]phenyl]ethanone
英文别名
1-[2-hydroxy-4-[3-(4-methoxyphenoxy)propoxy]phenyl]ethanone
1-[2-Hydroxy-4-[3-(4-methoxyphenoxy)propoxy]phenyl]ethanone化学式
CAS
63360-03-2
化学式
C18H20O5
mdl
——
分子量
316.354
InChiKey
JSVULXSFTDECCB-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:
    493.2±35.0 °C(Predicted)
  • 密度:
    1.176±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    23
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

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

  • 作为产物:
    参考文献:
    名称:
    Aryloxyalkyloxy- and aralkyloxy-4-hydroxy-3-nitrocoumarins which inhibit histamine release in the rat and also antagonize the effects of a slow reacting substance of anaphylaxis
    摘要:
    The syntheses and structure--activity relationships of a number of 4-hydroxy-3-nitrocoumarins, which are both antagonists of a slow reacting substance of anaphylaxis and potent inhibitors of antigen-induced histamine release in the rat, are described. Most active among these are 7-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy(-2-hydroxypropoxy] derivatives having hydrogen or lower alkyl substituents at the C-8 position of the coumarin ring, 168, 171, 173, and 174.
    DOI:
    10.1021/jm00188a007
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文献信息

  • Aryloxyalkyloxy- and aralkyloxy-4-hydroxy-3-nitrocoumarins which inhibit histamine release in the rat and also antagonize the effects of a slow reacting substance of anaphylaxis
    作者:Derek R. Buckle、D. James Outred、Janet W. Ross、Harry Smith、Raymond J. Smith、Barbara A. Spicer、Brian C. Gasson
    DOI:10.1021/jm00188a007
    日期:1979.2
    The syntheses and structure--activity relationships of a number of 4-hydroxy-3-nitrocoumarins, which are both antagonists of a slow reacting substance of anaphylaxis and potent inhibitors of antigen-induced histamine release in the rat, are described. Most active among these are 7-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy(-2-hydroxypropoxy] derivatives having hydrogen or lower alkyl substituents at the C-8 position of the coumarin ring, 168, 171, 173, and 174.
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