摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2,8-Dimethyl-non-8-en-4-ol | 154913-72-1

中文名称
——
中文别名
——
英文名称
2,8-Dimethyl-non-8-en-4-ol
英文别名
2,8-Dimethylnon-8-en-4-ol;2,8-dimethylnon-8-en-4-ol
2,8-Dimethyl-non-8-en-4-ol化学式
CAS
154913-72-1
化学式
C11H22O
mdl
——
分子量
170.295
InChiKey
NAXBKNMEFQNMIG-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):
    3.7
  • 重原子数:
    12
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    苯乙烯2,8-Dimethyl-non-8-en-4-ol 在 palladium diacetate 碳酸氢钠 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 以90%的产率得到6-Isobutyl-2-methyl-2-((E)-3-phenyl-allyl)-tetrahydro-pyran
    参考文献:
    名称:
    Catalytic tandem oxy-palladation and vinylation
    摘要:
    Intramolecular oxy-palladation of hydroxy-alkenes leads to organo-Pd(II) intermediates which can be trapped by alkenes in chain extension by vinyl substitution; catalysis is efficient using a reoxidation system but the process is limited to substrates which cannot undergo beta-hydride elimination from the organo-Pd(II) intermediate.
    DOI:
    10.1016/s0040-4039(00)79288-4
  • 作为产物:
    参考文献:
    名称:
    Catalytic tandem oxy-palladation and vinylation
    摘要:
    Intramolecular oxy-palladation of hydroxy-alkenes leads to organo-Pd(II) intermediates which can be trapped by alkenes in chain extension by vinyl substitution; catalysis is efficient using a reoxidation system but the process is limited to substrates which cannot undergo beta-hydride elimination from the organo-Pd(II) intermediate.
    DOI:
    10.1016/s0040-4039(00)79288-4
点击查看最新优质反应信息

文献信息

  • Catalytic tandem oxy-palladation and vinylation
    作者:M.F. Semmelhack、W.R. Epa
    DOI:10.1016/s0040-4039(00)79288-4
    日期:1993.11
    Intramolecular oxy-palladation of hydroxy-alkenes leads to organo-Pd(II) intermediates which can be trapped by alkenes in chain extension by vinyl substitution; catalysis is efficient using a reoxidation system but the process is limited to substrates which cannot undergo beta-hydride elimination from the organo-Pd(II) intermediate.
查看更多