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2-phenyl-3,3-bis(2,4,6-trimethylphenyl)spiro[4aH-1,2,3-benzodiazagermine-4,9'-fluorene] | 132775-02-1

中文名称
——
中文别名
——
英文名称
2-phenyl-3,3-bis(2,4,6-trimethylphenyl)spiro[4aH-1,2,3-benzodiazagermine-4,9'-fluorene]
英文别名
——
2-phenyl-3,3-bis(2,4,6-trimethylphenyl)spiro[4aH-1,2,3-benzodiazagermine-4,9'-fluorene]化学式
CAS
132775-02-1
化学式
C43H40GeN2
mdl
——
分子量
657.394
InChiKey
ZDZOLTGWVVJADZ-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):
    8.72
  • 重原子数:
    46.0
  • 可旋转键数:
    3.0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    15.6
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    2-phenyl-3,3-bis(2,4,6-trimethylphenyl)spiro[4aH-1,2,3-benzodiazagermine-4,9'-fluorene]乙醚 为溶剂, 生成 ((CH3)3C6H2)2Ge(CC12H8)(N(C6H5)NHC6H4)
    参考文献:
    名称:
    二聚芴基亚烷基与不饱和氮化合物的反应性
    摘要:
    Dimesitylfluorenylidenegermane (1) reacts with ethylbenzylideneamine (PhCH = NEt) to give, according to a [2 + 2] cycloaddition, the very thermally stable four-membered-ring germaazetidine 2. In contrast, imines with a NH function, such as (diphenylmethylidene)amine (Ph2C = NH), react only as protic reagents. A [2 + 4] cycloaddition is observed with azobenzene, affording 5, which slowly aromatizes to 6 or thermally rearranges to give the [2 + 2] cycloadduct germadiazetidine 7. In the case of nitrosobenzene, only the germanone dimer 17 and imine 9 have been observed, probably via the preliminary formation of transient four-membered heterocycle 15.
    DOI:
    10.1021/om00050a054
  • 作为产物:
    描述:
    (mesityl)2Ge(fluorenylidene)偶氮苯乙醚 为溶剂, 以58%的产率得到2-phenyl-3,3-bis(2,4,6-trimethylphenyl)spiro[4aH-1,2,3-benzodiazagermine-4,9'-fluorene]
    参考文献:
    名称:
    二聚芴基亚烷基与不饱和氮化合物的反应性
    摘要:
    Dimesitylfluorenylidenegermane (1) reacts with ethylbenzylideneamine (PhCH = NEt) to give, according to a [2 + 2] cycloaddition, the very thermally stable four-membered-ring germaazetidine 2. In contrast, imines with a NH function, such as (diphenylmethylidene)amine (Ph2C = NH), react only as protic reagents. A [2 + 4] cycloaddition is observed with azobenzene, affording 5, which slowly aromatizes to 6 or thermally rearranges to give the [2 + 2] cycloadduct germadiazetidine 7. In the case of nitrosobenzene, only the germanone dimer 17 and imine 9 have been observed, probably via the preliminary formation of transient four-membered heterocycle 15.
    DOI:
    10.1021/om00050a054
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