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5-cyanobenzocyclooctatetraene | 55277-76-4

中文名称
——
中文别名
——
英文名称
5-cyanobenzocyclooctatetraene
英文别名
——
5-cyanobenzocyclooctatetraene化学式
CAS
55277-76-4
化学式
C13H9N
mdl
——
分子量
179.221
InChiKey
NGWSSCIKVJGODW-KNJZMIIWSA-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):
    3.18
  • 重原子数:
    14.0
  • 可旋转键数:
    0.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    23.79
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    5-cyanobenzocyclooctatetraene 以42%的产率得到
    参考文献:
    名称:
    BENDER, CHRISTOPHER OWEN;CLYNE, DEAN SUTHERLAND;DOLMAN, DOUGLAS, CAN. J. CHEM., 69,(1991) N, C. 70-76
    摘要:
    DOI:
  • 作为产物:
    描述:
    5-cyanobenzosemibullvalene环己烷 为溶剂, 反应 0.5h, 以75%的产率得到5-cyanobenzocyclooctatetraene
    参考文献:
    名称:
    Bender, Christopher Owen; Clyne, Dean Sutherland; Dolman, Douglas, Canadian Journal of Chemistry, 1991, vol. 69, # 1, p. 70 - 76
    摘要:
    DOI:
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文献信息

  • Photochemistry of 4-cyano-2,3-benzobicyclo[4.2.0]octa-2,4,7-triene
    作者:Christopher Owen Bender、Douglas Dolman、Noah Tu
    DOI:10.1021/jo00017a007
    日期:1991.8
    4-Cyano-2,3-benzobicyclo[4.2.0]octa-2,4,7-triene (11) was found to be thermally and photochemically reactive. Heating solutions of 11 at 150-degrees-C for 2 h gave 5-cyanobenzocyclooctatetraene (10) quantitatively. The direct irradiation of triene 11 gave 2-cyanobenzosemibullvalene (i.e., SB 12, 63%, PHI = 0.067), COT 10 (28%, PHI = 0.031), and 1-cyanonaphthalene (ca. 0.5%, PHI = 0.0005). Upon sensitization with p-(dimethylamino)benzophenone, 11 gave 12 (30%, PHI = 0.028), COT 10 (9%, PHI = 0.0093), and 1-cyanonaphthalene (2%, PHI = 0.0018). Studies with deuterium-labeled triene (11a) revealed that the semibullavene produced from direct irradiation possessed a different label distribution to that obtained from sensitized irradiation, and hence state-dependent pathways operate in the SB formation. The mechanism proposed for the SB formation from S1 of 11 involves a 1,2-shift with cleavage of the cyclobutene C1-C6 bond of the triene, while SB formation from T1 results from a Zimmerman di-pi-methane rearrangement.
  • Bender,C.O. et al., Canadian Journal of Chemistry, 1978, vol. 56, p. 3027 - 3037
    作者:Bender,C.O. et al.
    DOI:——
    日期:——
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