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1,2-Bis<2-(2-formylbenzyl)benzyl>benzene | 154618-87-8

中文名称
——
中文别名
——
英文名称
1,2-Bis<2-(2-formylbenzyl)benzyl>benzene
英文别名
1,2-Bis[2-(2-formylbenzyl)benzyl]benzene;2-[[2-[[2-[[2-[(2-Formylphenyl)methyl]phenyl]methyl]phenyl]methyl]phenyl]methyl]benzaldehyde
1,2-Bis<2-(2-formylbenzyl)benzyl>benzene化学式
CAS
154618-87-8
化学式
C36H30O2
mdl
——
分子量
494.633
InChiKey
YRDAXPWSQUZJJP-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:
    651.5±50.0 °C(predicted)
  • 密度:
    1.149±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    8.5
  • 重原子数:
    38
  • 可旋转键数:
    10
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    描述:
    参考文献:
    名称:
    Orthocyclophanes. 3. Ketonands, Novel Ketonic Crowns of Polyoxo[1n]orthocyclophane Constitution
    摘要:
    Synthetic studies of a new family of novel ketonic macrocycles are reported. Exhaustive oxidation of all of the methylenes in odd-numbered [1(n)]orthocyclophanes ([1(n)]OCPs) resulted in the polyoxo derivatives of a cyclopolyorthobenzoyl or polyoxo[1(n)]orthocyclophane constitution. This new class of ketonic crowns is referred to as [1(n)]orthocyclophanepolyones and includes [1(5)] orthocyclophane-pentaone, [1(7)]orthocyclophaneheptaone, and [1(9)]orthocyclophanenonaone. We suggest the generic name ''ketonands'' for these ketonic crowns. Structures of ketonands were confirmed by spectral and X-ray crystallographic analyses.
    DOI:
    10.1021/jo00083a033
  • 作为产物:
    参考文献:
    名称:
    Orthocyclophanes. 3. Ketonands, Novel Ketonic Crowns of Polyoxo[1n]orthocyclophane Constitution
    摘要:
    Synthetic studies of a new family of novel ketonic macrocycles are reported. Exhaustive oxidation of all of the methylenes in odd-numbered [1(n)]orthocyclophanes ([1(n)]OCPs) resulted in the polyoxo derivatives of a cyclopolyorthobenzoyl or polyoxo[1(n)]orthocyclophane constitution. This new class of ketonic crowns is referred to as [1(n)]orthocyclophanepolyones and includes [1(5)] orthocyclophane-pentaone, [1(7)]orthocyclophaneheptaone, and [1(9)]orthocyclophanenonaone. We suggest the generic name ''ketonands'' for these ketonic crowns. Structures of ketonands were confirmed by spectral and X-ray crystallographic analyses.
    DOI:
    10.1021/jo00083a033
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文献信息

  • Orthocyclophanes. 4. Functionalization of [1n]Orthocyclophanes on the Aromatic Rings
    作者:Woo Young Lee、Chang Hee Park、Eun Hee Kim
    DOI:10.1021/jo00095a026
    日期:1994.8
    Functionalization of the [1(n)]orthocyclophanes ([1(n)]OCPs) has been accomplished by introducing groups on the aromatic rings of the cycles. Dilithiation of dibromoaromatic 10 followed by condensation with various aromatic dialdehydes, such as 14, 20, and 30, gave rise to [1(n)]OCP cycles bearing methoxy groups on the aromatic rings. Several polymethoxy[1(n)]OCPs have been prepared that are reasonably soluble inorganic solvents, in contrast to their parent hydrocarbons. Since methoxy functions can be converted to phenolic hydroxy groups and then to other functionalities, the methoxy derivatives may have broad applications to the modification of [1(n)]OCPs for the preparation of a variety of supramolecules.
  • Orthocyclophanes. 3. Ketonands, Novel Ketonic Crowns of Polyoxo[1n]orthocyclophane Constitution
    作者:Woo Young Lee、Chang Hee Park、Hyo-Joong Kim、Sangsoo Kim
    DOI:10.1021/jo00083a033
    日期:1994.2
    Synthetic studies of a new family of novel ketonic macrocycles are reported. Exhaustive oxidation of all of the methylenes in odd-numbered [1(n)]orthocyclophanes ([1(n)]OCPs) resulted in the polyoxo derivatives of a cyclopolyorthobenzoyl or polyoxo[1(n)]orthocyclophane constitution. This new class of ketonic crowns is referred to as [1(n)]orthocyclophanepolyones and includes [1(5)] orthocyclophane-pentaone, [1(7)]orthocyclophaneheptaone, and [1(9)]orthocyclophanenonaone. We suggest the generic name ''ketonands'' for these ketonic crowns. Structures of ketonands were confirmed by spectral and X-ray crystallographic analyses.
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