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tetrakis(triethylsilyl) diphosphate | 830326-70-0

中文名称
——
中文别名
——
英文名称
tetrakis(triethylsilyl) diphosphate
英文别名
Tetrakis(triethylsilyl) diphosphate;bis(triethylsilyloxy)phosphoryl bis(triethylsilyl) phosphate
tetrakis(triethylsilyl) diphosphate化学式
CAS
830326-70-0
化学式
C24H60O7P2Si4
mdl
——
分子量
635.026
InChiKey
UKGXSYIXIMIEPX-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):
    11.31
  • 重原子数:
    37
  • 可旋转键数:
    22
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    80.3
  • 氢给体数:
    0
  • 氢受体数:
    7

SDS

SDS:04d9adcf987831aff6357bad45b74fb9
查看

反应信息

  • 作为反应物:
    参考文献:
    名称:
    An efficient method for the preparation of silyl esters of diphosphoric, phosphoric, and phosphorous acid
    摘要:
    Tetrakis(trialkylsilyl) diphosphate (alkyl = Me, Et, iPr, tBu) can be obtained in quantitative yield by reacting commercial disodium dihydrogen diphosphate with the respective trialkyl chlorosilane in a triphasic system with formamide. The alkylsilane residues of the diphosphate silyl esters can be either partially or completely hydrolyzed without concurrent cleavage of the P-O-P bond of the diphosphate moiety. The method can be expanded to efficiently produce other persilylated or partially silylated phosphates and phosphites. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2013.12.024
  • 作为产物:
    描述:
    disodium pyrophoshate三乙基氯硅烷 以 formamide 为溶剂, 反应 4.0h, 以96%的产率得到tetrakis(triethylsilyl) diphosphate
    参考文献:
    名称:
    An efficient method for the preparation of silyl esters of diphosphoric, phosphoric, and phosphorous acid
    摘要:
    Tetrakis(trialkylsilyl) diphosphate (alkyl = Me, Et, iPr, tBu) can be obtained in quantitative yield by reacting commercial disodium dihydrogen diphosphate with the respective trialkyl chlorosilane in a triphasic system with formamide. The alkylsilane residues of the diphosphate silyl esters can be either partially or completely hydrolyzed without concurrent cleavage of the P-O-P bond of the diphosphate moiety. The method can be expanded to efficiently produce other persilylated or partially silylated phosphates and phosphites. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2013.12.024
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