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2-Allyloxy-heptadecan-1-ol | 81861-44-1

中文名称
——
中文别名
——
英文名称
2-Allyloxy-heptadecan-1-ol
英文别名
——
2-Allyloxy-heptadecan-1-ol化学式
CAS
81861-44-1
化学式
C20H40O2
mdl
——
分子量
312.536
InChiKey
QRUAHGRKSPWQBI-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):
    6.03
  • 重原子数:
    22.0
  • 可旋转键数:
    18.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    29.46
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    2-Allyloxy-heptadecan-1-olpotassium carbonate 作用下, 以 乙醚 为溶剂, 生成 2-(iodomethyl)-5-pentadecyl-1,4-dioxane
    参考文献:
    名称:
    Darmstoff analogs. 2. Ring and side chain effects on smooth muscle contraction
    摘要:
    2-cis-delta 8-Heptadecenyl-4-(hydroxymethyl)-1,3-dioxolane monosodium phosphate (1b) has been shown to be present as a major component of Darmstoff in mammalian intestine and to be a potent inducer for contraction of intestinal smooth muscle. The analogous 2-pentadecyl material 1a, also found abundantly in the intestine, is inactive. In this study, synthesis of phosphorylated hydroxymethyl-1,4-dioxanes, -tetrahydrofurans, -cyclopentanes, and -oxathiolanes bearing both oleyl and palmityl side chains is reported. Of these, 2-(hydroxymethyl)-5-cis-delta 8-heptadecenyl-1,4-dioxane monosodium phosphate (2b) exhibits about 12% of the activity of 1b. Its pentadecyl analogue 2a, like 1a, is totally inactive, as are all other compounds prepared. The results indicate that Darmstoff-like compounds exhibit specific chemical requirements for activity and that where activity is encountered, the side-chain specificity noted in 1a and 1b can be preserved.
    DOI:
    10.1021/jm00344a006
  • 作为产物:
    描述:
    2-hydroxyheptadecanoic acid 在 lithium aluminium tetrahydride 、 乙酰氯silver(l) oxide 作用下, 以 乙醚 为溶剂, 反应 36.5h, 生成 2-Allyloxy-heptadecan-1-ol
    参考文献:
    名称:
    Darmstoff analogs. 2. Ring and side chain effects on smooth muscle contraction
    摘要:
    2-cis-delta 8-Heptadecenyl-4-(hydroxymethyl)-1,3-dioxolane monosodium phosphate (1b) has been shown to be present as a major component of Darmstoff in mammalian intestine and to be a potent inducer for contraction of intestinal smooth muscle. The analogous 2-pentadecyl material 1a, also found abundantly in the intestine, is inactive. In this study, synthesis of phosphorylated hydroxymethyl-1,4-dioxanes, -tetrahydrofurans, -cyclopentanes, and -oxathiolanes bearing both oleyl and palmityl side chains is reported. Of these, 2-(hydroxymethyl)-5-cis-delta 8-heptadecenyl-1,4-dioxane monosodium phosphate (2b) exhibits about 12% of the activity of 1b. Its pentadecyl analogue 2a, like 1a, is totally inactive, as are all other compounds prepared. The results indicate that Darmstoff-like compounds exhibit specific chemical requirements for activity and that where activity is encountered, the side-chain specificity noted in 1a and 1b can be preserved.
    DOI:
    10.1021/jm00344a006
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文献信息

  • Darmstoff analogs. 2. Ring and side chain effects on smooth muscle contraction
    作者:Robert A. Wiley、Wayne T. Harris、Catherine Brungardt、Michael Marx
    DOI:10.1021/jm00344a006
    日期:1982.2
    2-cis-delta 8-Heptadecenyl-4-(hydroxymethyl)-1,3-dioxolane monosodium phosphate (1b) has been shown to be present as a major component of Darmstoff in mammalian intestine and to be a potent inducer for contraction of intestinal smooth muscle. The analogous 2-pentadecyl material 1a, also found abundantly in the intestine, is inactive. In this study, synthesis of phosphorylated hydroxymethyl-1,4-dioxanes, -tetrahydrofurans, -cyclopentanes, and -oxathiolanes bearing both oleyl and palmityl side chains is reported. Of these, 2-(hydroxymethyl)-5-cis-delta 8-heptadecenyl-1,4-dioxane monosodium phosphate (2b) exhibits about 12% of the activity of 1b. Its pentadecyl analogue 2a, like 1a, is totally inactive, as are all other compounds prepared. The results indicate that Darmstoff-like compounds exhibit specific chemical requirements for activity and that where activity is encountered, the side-chain specificity noted in 1a and 1b can be preserved.
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