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3,9-Dichloro-chrysene | 36288-16-1

中文名称
——
中文别名
——
英文名称
3,9-Dichloro-chrysene
英文别名
3,9-Dichlorochrysene
3,9-Dichloro-chrysene化学式
CAS
36288-16-1
化学式
C18H10Cl2
mdl
——
分子量
297.183
InChiKey
ZRNJCWGDFQRPAN-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):
    6.9
  • 重原子数:
    20
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    (E,E,E)-1,6-di(4-chlorophenyl)hexa-1,3,5-triene 在 作用下, 以 为溶剂, 生成 3,9-Dichloro-chrysene
    参考文献:
    名称:
    Photocyclization Reactions of Aryl Polyenes. V. Photochemical Synthesis of Substituted Chrysenes
    摘要:
    1,6-二对位取代苯基-1,3,5-己三烯的光环化-氧化反应产生了3,9-二取代蒽。类似地,对1-对位取代苯基-6-苯基-1,3,5-己三烯的辐射处理产生了3-取代蒽。通过1-α-萘基-2-对位取代苯乙烯的光环化-氧化,高产率地独立制备了3-取代蒽。
    DOI:
    10.1139/v72-081
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文献信息

  • COMPOUND FOR ORGANIC THIN FILM TRANSISTOR AND ORGANIC THIN FILM TRANSISTOR USING THE SAME
    申请人:Nakano Yuki
    公开号:US20110210319A1
    公开(公告)日:2011-09-01
    A compound for an organic thin film transistor represented by the following formula ( 1 ): wherein at least one pair of adjacent two groups of R 1 , R 3 , R 5 and R 7 is bonded to each other to form a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 60 carbon atoms or a substituted or unsubstituted aromatic heterocyclic ring having 3 to 60 carbon atoms, the ring being fused to the ring to which the groups are bonded; and at least one pair of adjacent two groups of R 2 , R 4 , R 6 and R 8 is bonded to each other to form a substituted or unsubstituted aromatic hydrocarbon ring having 6 to 60 carbon atoms or a substituted or unsubstituted aromatic heterocyclic ring having 3 to 60 carbon atoms, the ring being fused to the ring to which the groups are bonded.
  • US8785915B2
    申请人:——
    公开号:US8785915B2
    公开(公告)日:2014-07-22
  • Photocyclization Reactions of Aryl Polyenes. V. Photochemical Synthesis of Substituted Chrysenes
    作者:Clifford C. Leznoff、Roger J. Hayward
    DOI:10.1139/v72-081
    日期:1972.2.15

    The photocyclization-oxidation reaction of 1,6-di-p-substituted-phenyl-1,3,5-hexatrienes gave 3,9-disubstituted-chrysenes. Similarly, irradiation of 1-p-substituted-phenyl-6-phenyl-1,3,5-hexatrienes yielded 3-substituted-chrysenes. The 3-substituted-chrysenes were independently prepared in a high yield by the photocyclization-oxidation of 1-α-naphthyl-2-p-substituted-phenylethylenes.

    1,6-二对位取代苯基-1,3,5-己三烯的光环化-氧化反应产生了3,9-二取代蒽。类似地,对1-对位取代苯基-6-苯基-1,3,5-己三烯的辐射处理产生了3-取代蒽。通过1-α-萘基-2-对位取代苯乙烯的光环化-氧化,高产率地独立制备了3-取代蒽。
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