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3-(3-noradamantyl)-3-pentanol | 1404321-33-0

中文名称
——
中文别名
——
英文名称
3-(3-noradamantyl)-3-pentanol
英文别名
——
3-(3-noradamantyl)-3-pentanol化学式
CAS
1404321-33-0
化学式
C14H24O
mdl
——
分子量
208.344
InChiKey
GVRYHTSDKCBTNB-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):
    3.36
  • 重原子数:
    15.0
  • 可旋转键数:
    3.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.23
  • 氢给体数:
    1.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    3-(3-noradamantyl)-3-pentanol盐酸硫酸溶剂黄146硫脲 作用下, 以 乙醚乙醇 为溶剂, 反应 24.0h, 生成 (2,2-diethyladamant-1-yl)amine hydrochloride
    参考文献:
    名称:
    Synthesis and Anti-influenza A Virus Activity of 2,2-Dialkylamantadines and Related Compounds
    摘要:
    The synthesis of several 2,2-dialkyladamantyl-1-amines through the combination of a Ritter reaction with a Wagner-Meerwein rearrangement from noradamantane alcohols is reported. Several of the novel amines displayed low micromolar activities against several H1N1 influenza virus strains, including the amantadine-resistant A/PuertoRico/8/34 strain. Most of the compounds did not show cytotoxicity for MDCK cells.
    DOI:
    10.1021/ml300279b
  • 作为产物:
    描述:
    乙基锂methyl tricyclo[3.3.1.0(3,7)]nonane-3-carboxylate乙醚 为溶剂, 反应 1.0h, 以56%的产率得到3-(3-noradamantyl)-3-pentanol
    参考文献:
    名称:
    Synthesis and Anti-influenza A Virus Activity of 2,2-Dialkylamantadines and Related Compounds
    摘要:
    The synthesis of several 2,2-dialkyladamantyl-1-amines through the combination of a Ritter reaction with a Wagner-Meerwein rearrangement from noradamantane alcohols is reported. Several of the novel amines displayed low micromolar activities against several H1N1 influenza virus strains, including the amantadine-resistant A/PuertoRico/8/34 strain. Most of the compounds did not show cytotoxicity for MDCK cells.
    DOI:
    10.1021/ml300279b
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