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18,39-Ditert-butyldecacyclo[20.20.0.02,15.03,8.09,14.016,21.023,36.024,29.030,35.037,42]dotetraconta-1(22),2(15),3,5,7,9,11,13,16(21),17,19,23(36),24,26,28,30,32,34,37(42),38,40-henicosaene | 1325730-21-9

中文名称
——
中文别名
——
英文名称
18,39-Ditert-butyldecacyclo[20.20.0.02,15.03,8.09,14.016,21.023,36.024,29.030,35.037,42]dotetraconta-1(22),2(15),3,5,7,9,11,13,16(21),17,19,23(36),24,26,28,30,32,34,37(42),38,40-henicosaene
英文别名
18,39-ditert-butyldecacyclo[20.20.0.02,15.03,8.09,14.016,21.023,36.024,29.030,35.037,42]dotetraconta-1(22),2(15),3,5,7,9,11,13,16(21),17,19,23(36),24,26,28,30,32,34,37(42),38,40-henicosaene
18,39-Ditert-butyldecacyclo[20.20.0.02,15.03,8.09,14.016,21.023,36.024,29.030,35.037,42]dotetraconta-1(22),2(15),3,5,7,9,11,13,16(21),17,19,23(36),24,26,28,30,32,34,37(42),38,40-henicosaene化学式
CAS
1325730-21-9
化学式
C50H40
mdl
——
分子量
640.868
InChiKey
DWKMVNSEJOXUPH-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):
    14.9
  • 重原子数:
    50
  • 可旋转键数:
    2
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

上下游信息

  • 下游产品
    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:
    Synthesis of Large Polycyclic Aromatic Hydrocarbons from Bis(biaryl)acetylenes: Large Planar PAHs with Low π-Sextets
    摘要:
    A new synthesis of large PAHs with low Clar sextets was developed. This synthesis involves initial bis(biaryl)acetylene 1, which undergoes initial ICI-aromatization and a subsequent Mizoroki-Heck coupling reaction to give dibenzochrysene derivative 3 that can be transformed into planar PAHs 4 using DDQ-oxidation.
    DOI:
    10.1021/ol201854g
  • 作为产物:
    描述:
    C50H41I 在 trans-bis(triphenylphosphine)palladium dichloride 、 sodium carbonate 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 12.0h, 以86%的产率得到18,39-Ditert-butyldecacyclo[20.20.0.02,15.03,8.09,14.016,21.023,36.024,29.030,35.037,42]dotetraconta-1(22),2(15),3,5,7,9,11,13,16(21),17,19,23(36),24,26,28,30,32,34,37(42),38,40-henicosaene
    参考文献:
    名称:
    Synthesis of Large Polycyclic Aromatic Hydrocarbons from Bis(biaryl)acetylenes: Large Planar PAHs with Low π-Sextets
    摘要:
    A new synthesis of large PAHs with low Clar sextets was developed. This synthesis involves initial bis(biaryl)acetylene 1, which undergoes initial ICI-aromatization and a subsequent Mizoroki-Heck coupling reaction to give dibenzochrysene derivative 3 that can be transformed into planar PAHs 4 using DDQ-oxidation.
    DOI:
    10.1021/ol201854g
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文献信息

  • Synthesis of Large Polycyclic Aromatic Hydrocarbons from Bis(biaryl)acetylenes: Large Planar PAHs with Low π-Sextets
    作者:Tse-An Chen、Rai-Shung Liu
    DOI:10.1021/ol201854g
    日期:2011.9.2
    A new synthesis of large PAHs with low Clar sextets was developed. This synthesis involves initial bis(biaryl)acetylene 1, which undergoes initial ICI-aromatization and a subsequent Mizoroki-Heck coupling reaction to give dibenzochrysene derivative 3 that can be transformed into planar PAHs 4 using DDQ-oxidation.
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