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tetrahydrodicyclobutapyrene | 143901-48-8

中文名称
——
中文别名
——
英文名称
tetrahydrodicyclobutapyrene
英文别名
tetrahydrodicyclobuta[e,l]pyrene;Hexacyclo[8.8.2.02,5.06,20.011,14.015,19]icosa-1(18),2(5),6,8,10,14,16,19-octaene
tetrahydrodicyclobuta<e,l>pyrene化学式
CAS
143901-48-8
化学式
C20H14
mdl
——
分子量
254.331
InChiKey
GFUVMTMAJKRRGD-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

物化性质

  • 沸点:
    485.4±40.0 °C(Predicted)
  • 密度:
    1.377±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    20
  • 可旋转键数:
    0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    tetrahydrodicyclobutapyrene马来酸二乙酯邻苯二甲酸二乙酯 作用下, 反应 1.0h, 以96%的产率得到
    参考文献:
    名称:
    Synthesis and properties of dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene
    摘要:
    Dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene were prepared by the sequence of photo-cycloaddition of stryene derivatives, transannulation, and aromatization through lithiation. They reacted with dienophiles at 180-degrees-C to afford Diels-Alder adducts in excellent yields.
    DOI:
    10.1021/jo00048a031
  • 作为产物:
    描述:
    正丁基锂四甲基乙二胺 作用下, 以 正己烷环己烷 为溶剂, 以10%的产率得到tetrahydrodicyclobutapyrene
    参考文献:
    名称:
    Synthesis and properties of dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene
    摘要:
    Dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene were prepared by the sequence of photo-cycloaddition of stryene derivatives, transannulation, and aromatization through lithiation. They reacted with dienophiles at 180-degrees-C to afford Diels-Alder adducts in excellent yields.
    DOI:
    10.1021/jo00048a031
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文献信息

  • Synthesis and properties of dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene
    作者:Yasuhiro Wada、Tetsuya Tago、Katsuyuki Sugata、Jun Nishimura
    DOI:10.1021/jo00048a031
    日期:1992.10
    Dihydrocyclobuta[e]pyrene and tetrahydrodicyclobuta[e,l]pyrene were prepared by the sequence of photo-cycloaddition of stryene derivatives, transannulation, and aromatization through lithiation. They reacted with dienophiles at 180-degrees-C to afford Diels-Alder adducts in excellent yields.
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