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3,15-diphenyl-7,11,18,21-tetraoxatrispiro[5.2.2.5.2.2]henicosane

中文名称
——
中文别名
——
英文名称
3,15-diphenyl-7,11,18,21-tetraoxatrispiro[5.2.2.5.2.2]henicosane
英文别名
3,15-diphenyl-7,11,18,21-tetraoxatrispiro[5.2.2.512.29.26]henicosane
3,15-diphenyl-7,11,18,21-tetraoxatrispiro[5.2.2.5.2.2]henicosane化学式
CAS
——
化学式
C29H36O4
mdl
——
分子量
448.602
InChiKey
YWEQKRAKRJARNU-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):
    5.2
  • 重原子数:
    33
  • 可旋转键数:
    2
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    季戊四醇4-苯基环己酮对甲苯磺酸 作用下, 以 为溶剂, 以75%的产率得到3,15-diphenyl-7,11,18,21-tetraoxatrispiro[5.2.2.5.2.2]henicosane
    参考文献:
    名称:
    Synthesis and Stereochemistry of Some New Trispiro-1,3-dioxaneswith Axial and Helical Chirality
    摘要:
    The stereoisomerism of some trispiro-1,3-dioxanes obtained from substituted cyclohexanones and pentaerithrytol is discussed considering the possible trispiro-6,9-syn-9,12-syn, trispiro-6,9-syn-9,12-anti, and trispiro-6,9-anti-9,12-anti structures of the spiro skeleton and the characteristic axial and helical chirality of spiranes with six-membered rings. The influence of the presence of chiral carbon atoms and of the peculiar conformational behaviour of the molecules on the stereoisomerism of the these compounds is elucidated.
    DOI:
    10.1007/pl00010105
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文献信息

  • Synthesis and Stereochemistry of Some New Trispiro-1,3-dioxaneswith Axial and Helical Chirality
    作者:Ion Grosu、Sorin Mager、Gerard Plé、Istvan Turos、Eugen Mesaros、Iosefina Schirger
    DOI:10.1007/pl00010105
    日期:1998.1
    The stereoisomerism of some trispiro-1,3-dioxanes obtained from substituted cyclohexanones and pentaerithrytol is discussed considering the possible trispiro-6,9-syn-9,12-syn, trispiro-6,9-syn-9,12-anti, and trispiro-6,9-anti-9,12-anti structures of the spiro skeleton and the characteristic axial and helical chirality of spiranes with six-membered rings. The influence of the presence of chiral carbon atoms and of the peculiar conformational behaviour of the molecules on the stereoisomerism of the these compounds is elucidated.
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