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二(萘-2-基)二乙基亚磷酰胺 | 64919-04-6

中文名称
二(萘-2-基)二乙基亚磷酰胺
中文别名
——
英文名称
N-dinaphthalen-2-yloxyphosphanyl-N-ethylethanamine
英文别名
——
二(萘-2-基)二乙基亚磷酰胺化学式
CAS
64919-04-6
化学式
C24H24NO2P
mdl
——
分子量
389.434
InChiKey
BUVBSDKSQJNKHV-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:
    519.3±33.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.1
  • 重原子数:
    28
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    21.7
  • 氢给体数:
    0
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    描述:
    二(萘-2-基)二乙基亚磷酰胺 在 sulfur 作用下, 以 乙腈 为溶剂, 反应 40.0h, 生成 Diethyl-thiophosphoramidic acid O,O'-dinaphthalen-2-yl ester
    参考文献:
    名称:
    Dismutation of arylene phosphorodiamidites: Specific features and aspects of preparative use
    摘要:
    The dismutation ofarylene phosphorodiamidites derived from the simplest phenols and naphthols and of their dibasic analogs was studied. The main regular trends of this process and the limits of its synthetic applicability were determined.
    DOI:
    10.1134/s1070363206020046
  • 作为产物:
    参考文献:
    名称:
    Dismutation of Diamidoarylphosphites
    摘要:
    Some examples of spontaneous dismutation of diamidoarylphosphites in different solvents were studied, and features of the process were revealed.
    DOI:
    10.1080/714040960
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文献信息

  • Dismutation of Diamidoarylphosphites
    作者:Edward E. Nifantyev、Elena N. Rasadkina、Pavel V. Slitikov、Larisa K. Vasyanina
    DOI:10.1080/714040960
    日期:2003.11.1
    Some examples of spontaneous dismutation of diamidoarylphosphites in different solvents were studied, and features of the process were revealed.
  • US7253298B2
    申请人:——
    公开号:US7253298B2
    公开(公告)日:2007-08-07
  • Dismutation of arylene phosphorodiamidites: Specific features and aspects of preparative use
    作者:E. N. Rasadkina、P. V. Slitikov、E. E. Nifant’ev
    DOI:10.1134/s1070363206020046
    日期:2006.2
    The dismutation ofarylene phosphorodiamidites derived from the simplest phenols and naphthols and of their dibasic analogs was studied. The main regular trends of this process and the limits of its synthetic applicability were determined.
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