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4-[7-[(1,1-Dimethylethyl)dimethylsilyl]oxy 8-(3-Methyl-2-buten-1-yl)cannflavin B | 1030601-60-5

中文名称
——
中文别名
——
英文名称
4-[7-[(1,1-Dimethylethyl)dimethylsilyl]oxy 8-(3-Methyl-2-buten-1-yl)cannflavin B
英文别名
[4-[7-[tert-butyl(dimethyl)silyl]oxy-5-hydroxy-8-(3-methylbut-2-enyl)-4-oxochromen-2-yl]-2-methoxyphenyl] 2,2-dimethylpropanoate
4-[7-[(1,1-Dimethylethyl)dimethylsilyl]oxy 8-(3-Methyl-2-buten-1-yl)cannflavin B化学式
CAS
1030601-60-5
化学式
C32H42O7Si
mdl
——
分子量
566.767
InChiKey
IVPSHCUMSGEBFF-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):
    8.02
  • 重原子数:
    40
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    91.3
  • 氢给体数:
    1
  • 氢受体数:
    7

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

  • 作为产物:
    描述:
    1-[2,4-bis(tert-butyldimethylsilyloxy)-6-hydroxy-3-prenylphenyl]-3-(4-pivaloyloxy-3-methoxyphenyl)-1,3-propanedione三甲基氯硅烷 、 copper dichloride 、 作用下, 以 乙腈 为溶剂, 反应 1.5h, 以60%的产率得到7-O-tert-butyldimethylsilyl-4'-O-pivaloylcannflavin B
    参考文献:
    名称:
    A Regiodivergent Synthesis of Ring A C-Prenylflavones
    摘要:
    Capitalizing on the use of orthogonal protecting groups and the development of a modified Robinson flavone synthesis that avoids harsh acidic conditions, a regioselective synthesis of 6- and 8-prenylflavones from the same prenylated disilylated phloracetophenone (9) has been developed, targeting cannflavin B (1d), the COX-inhibiting principle of marijuana, and its unnatural isomer isocannflavin B (1e) as model compounds.
    DOI:
    10.1021/ol800665w
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文献信息

  • A Regiodivergent Synthesis of Ring A C-Prenylflavones
    作者:Alberto Minassi、Anna Giana、Abdellah Ech-Chahad、Giovanni Appendino
    DOI:10.1021/ol800665w
    日期:2008.6.5
    Capitalizing on the use of orthogonal protecting groups and the development of a modified Robinson flavone synthesis that avoids harsh acidic conditions, a regioselective synthesis of 6- and 8-prenylflavones from the same prenylated disilylated phloracetophenone (9) has been developed, targeting cannflavin B (1d), the COX-inhibiting principle of marijuana, and its unnatural isomer isocannflavin B (1e) as model compounds.
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