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2,4,6,8-Tetrakis(hydroxymethyl)-9,9-dimethyl-2,4,6,8-tetrazabicyclo[3.3.1]nonane-3,7-dione | 34224-03-8

中文名称
——
中文别名
——
英文名称
2,4,6,8-Tetrakis(hydroxymethyl)-9,9-dimethyl-2,4,6,8-tetrazabicyclo[3.3.1]nonane-3,7-dione
英文别名
——
2,4,6,8-Tetrakis(hydroxymethyl)-9,9-dimethyl-2,4,6,8-tetrazabicyclo[3.3.1]nonane-3,7-dione化学式
CAS
34224-03-8
化学式
C11H20N4O6
mdl
——
分子量
304.303
InChiKey
YZLLZCQPHOBSRY-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):
    -0.9
  • 重原子数:
    21
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    128
  • 氢给体数:
    4
  • 氢受体数:
    6

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:
    2,4,6,8-Tetrakis(hydroxymethyl)-9,9-dimethyl-2,4,6,8-tetrazabicyclo[3.3.1]nonane-3,7-dione盐酸三氯化铝氯化亚砜 作用下, 以 二氯甲烷 为溶剂, 反应 33.0h, 生成 2,6-dibenzyl-9,9-dimethyl-2,4,6,8-tetraazabicyclo[3.3.1]nonane-3,7-dione
    参考文献:
    名称:
    Molecular Clips Based on Propanediurea. Exceptionally High Binding Affinities for Resorcinol Guests
    摘要:
    A series of new receptor molecules derived from 2,4,6,8-tetraazabicyclo [3.3.1]nonane-3,7-dione (propanediurea) is described. These molecules possess a cavity which is defined by two nearly parallel aromatic side walls positioned on top of a bis-urea framework. The resulting "U-shaped" clip molecules are ideal hosts for the complexation of flat aromatic guest molecules. The affinity of these new propanediurea based molecular clips for dihydroxybenzene derivatives is exceptionally high, with association constants up to K-a = 2 400 000 L mol(-1). Comparison of the binding mechanism of a variety of clip and half clip hosts, in conjunction with NMR, IR, and X-ray studies, has enabled the reason for this high binding to be elucidated. It is shown that subtle sub-angstrom changes in the geometry of the clip molecules have a great impact on their binding properties.
    DOI:
    10.1021/jo001317k
  • 作为产物:
    参考文献:
    名称:
    Molecular Clips Based on Propanediurea. Exceptionally High Binding Affinities for Resorcinol Guests
    摘要:
    A series of new receptor molecules derived from 2,4,6,8-tetraazabicyclo [3.3.1]nonane-3,7-dione (propanediurea) is described. These molecules possess a cavity which is defined by two nearly parallel aromatic side walls positioned on top of a bis-urea framework. The resulting "U-shaped" clip molecules are ideal hosts for the complexation of flat aromatic guest molecules. The affinity of these new propanediurea based molecular clips for dihydroxybenzene derivatives is exceptionally high, with association constants up to K-a = 2 400 000 L mol(-1). Comparison of the binding mechanism of a variety of clip and half clip hosts, in conjunction with NMR, IR, and X-ray studies, has enabled the reason for this high binding to be elucidated. It is shown that subtle sub-angstrom changes in the geometry of the clip molecules have a great impact on their binding properties.
    DOI:
    10.1021/jo001317k
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文献信息

  • Molecular Clips Based on Propanediurea. Exceptionally High Binding Affinities for Resorcinol Guests
    作者:Rob J. Jansen、René de Gelder、Alan E. Rowan、Hans W. Scheeren、Roeland J. M. Nolte
    DOI:10.1021/jo001317k
    日期:2001.4.1
    A series of new receptor molecules derived from 2,4,6,8-tetraazabicyclo [3.3.1]nonane-3,7-dione (propanediurea) is described. These molecules possess a cavity which is defined by two nearly parallel aromatic side walls positioned on top of a bis-urea framework. The resulting "U-shaped" clip molecules are ideal hosts for the complexation of flat aromatic guest molecules. The affinity of these new propanediurea based molecular clips for dihydroxybenzene derivatives is exceptionally high, with association constants up to K-a = 2 400 000 L mol(-1). Comparison of the binding mechanism of a variety of clip and half clip hosts, in conjunction with NMR, IR, and X-ray studies, has enabled the reason for this high binding to be elucidated. It is shown that subtle sub-angstrom changes in the geometry of the clip molecules have a great impact on their binding properties.
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