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(4S,6S,8S,10R,12R,14R)-4,6,8,14-tetramethoxy-1-nonadecene-10,12-diol | 131435-83-1

中文名称
——
中文别名
——
英文名称
(4S,6S,8S,10R,12R,14R)-4,6,8,14-tetramethoxy-1-nonadecene-10,12-diol
英文别名
——
(4S,6S,8S,10R,12R,14R)-4,6,8,14-tetramethoxy-1-nonadecene-10,12-diol化学式
CAS
131435-83-1
化学式
C23H46O6
mdl
——
分子量
418.615
InChiKey
CROUCFVBPVKCSB-WQANTMLLSA-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):
    3.88
  • 重原子数:
    29.0
  • 可旋转键数:
    20.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    77.38
  • 氢给体数:
    2.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    (4S,6S,8S,10R,12R,14R)-4,6,8,14-tetramethoxy-1-nonadecene-10,12-diol碘甲烷 在 potassium hydride 作用下, 以 四氢呋喃 为溶剂, 以91%的产率得到(4S,6S,8S,10R,12R,14R)-4,6,8,10,12,14-hexamethoxy-1-nonadecene
    参考文献:
    名称:
    Isotactic polymethoxy 1-alkenes from blue-green algae. Synthesis and absolute stereochemistry
    摘要:
    Novel isotactic polymethoxy-1-alkenes 1-4 were isolated from tolytoxin-producing blue-green algae belonging to the family Scytonemataceae. Scytonema mirabile produced 1 and 2, whereas 3 and 4 were isolated from S. burmanicum. The gross structures and relative stereochemistries were determined by mass and NMR spectral analyses. The absolute configurations of 1-4 were established by direct comparison with optically active synthetic samples.
    DOI:
    10.1021/jo00002a027
  • 作为产物:
    描述:
    (4S,6S,8S,10S,14R)-12-oxo-4,6,8,14-tetramethoxy-1-nonadecen-10-ol 在 sodium tetrahydroborate 、 二乙基甲氧基硼烷 作用下, 以 四氢呋喃甲醇 为溶剂, 以91%的产率得到(4S,6S,8S,10R,12R,14R)-4,6,8,14-tetramethoxy-1-nonadecene-10,12-diol
    参考文献:
    名称:
    Isotactic polymethoxy 1-alkenes from blue-green algae. Synthesis and absolute stereochemistry
    摘要:
    Novel isotactic polymethoxy-1-alkenes 1-4 were isolated from tolytoxin-producing blue-green algae belonging to the family Scytonemataceae. Scytonema mirabile produced 1 and 2, whereas 3 and 4 were isolated from S. burmanicum. The gross structures and relative stereochemistries were determined by mass and NMR spectral analyses. The absolute configurations of 1-4 were established by direct comparison with optically active synthetic samples.
    DOI:
    10.1021/jo00002a027
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