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7α-oxohexahydrocannabinol acetate | 91385-20-5

中文名称
——
中文别名
——
英文名称
7α-oxohexahydrocannabinol acetate
英文别名
——
7α-oxohexahydrocannabinol acetate化学式
CAS
91385-20-5
化学式
C23H32O4
mdl
——
分子量
372.505
InChiKey
OSLVHXPECIGVGG-IPMKNSEASA-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):
    5.21
  • 重原子数:
    27.0
  • 可旋转键数:
    6.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.65
  • 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:
    参考文献:
    名称:
    Activity of novel aminocannabinoids in baboons
    摘要:
    The axial and equatorial isomers of 7-(methylamino)hexahydrocannabinol (1 and 2) and 7-(dimethylamino)hexahydrocannabinol (3 and 4) were prepared by reductive amination of the corresponding cannabinoid aldehydes. The amines caused some tranquility in baboons but did not evoke the typical cannabimimetic syndrome caused by psychoactive cannabinoids. However the axial amines (1 and 3) but not the equatorial ones (2 and 4) caused bouts of scratching and yawning. The latter is a rare pharmacological effect hitherto not observed with other cannabinoids.
    DOI:
    10.1021/jm00376a029
  • 作为产物:
    描述:
    (-)-9-nor-9-formyl-Δ8-tetrahydrocannabinol acetate 在 palladium on activated charcoal 氢气 作用下, 以 乙醇 为溶剂, 反应 48.0h, 以34.6%的产率得到7α-oxohexahydrocannabinol acetate
    参考文献:
    名称:
    Activity of novel aminocannabinoids in baboons
    摘要:
    The axial and equatorial isomers of 7-(methylamino)hexahydrocannabinol (1 and 2) and 7-(dimethylamino)hexahydrocannabinol (3 and 4) were prepared by reductive amination of the corresponding cannabinoid aldehydes. The amines caused some tranquility in baboons but did not evoke the typical cannabimimetic syndrome caused by psychoactive cannabinoids. However the axial amines (1 and 3) but not the equatorial ones (2 and 4) caused bouts of scratching and yawning. The latter is a rare pharmacological effect hitherto not observed with other cannabinoids.
    DOI:
    10.1021/jm00376a029
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