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1-(1-pyrrolyl)ethyl bis(2-phenylethyl)diselenophosphinate | 1351415-43-4

中文名称
——
中文别名
——
英文名称
1-(1-pyrrolyl)ethyl bis(2-phenylethyl)diselenophosphinate
英文别名
Bis(2-phenylethyl)-(1-pyrrol-1-ylethylselanyl)-selenidophosphanium;bis(2-phenylethyl)-(1-pyrrol-1-ylethylselanyl)-selenidophosphanium
1-(1-pyrrolyl)ethyl bis(2-phenylethyl)diselenophosphinate化学式
CAS
1351415-43-4
化学式
C22H26NPSe2
mdl
——
分子量
493.349
InChiKey
WMWPEOBIGQFNHD-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):
    5.21
  • 重原子数:
    26
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    4.9
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    1-乙烯-1H-吡咯bis(2-phenethyl)phosphineselenium 作用下, 以 1,4-二氧六环 为溶剂, 反应 3.0h, 以95%的产率得到1-(1-pyrrolyl)ethyl bis(2-phenylethyl)diselenophosphinate
    参考文献:
    名称:
    A three-component reaction between alkenes, secondary phosphanes, and elemental selenium: a novel, efficient, atom-economic synthesis of diselenophosphinic esters
    摘要:
    A novel, convenient, atom-economic approach toward the synthesis of diselenophosphinic esters has been developed via the three-component reaction between aryl- or hetarylalkenes secondary phosphanes, and elemental selenium. The reaction proceeds without a catalyst (85 degrees C, 3 h, 1,4-dioxane) to afford the target compounds in good to high yields. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2011.10.094
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文献信息

  • A three-component reaction between alkenes, secondary phosphanes, and elemental selenium: a novel, efficient, atom-economic synthesis of diselenophosphinic esters
    作者:Nina K. Gusarova、Alexander V. Artem’ev、Svetlana F. Malysheva、Ol’ga A. Tarasova、Boris A. Trofimov
    DOI:10.1016/j.tetlet.2011.10.094
    日期:2011.12
    A novel, convenient, atom-economic approach toward the synthesis of diselenophosphinic esters has been developed via the three-component reaction between aryl- or hetarylalkenes secondary phosphanes, and elemental selenium. The reaction proceeds without a catalyst (85 degrees C, 3 h, 1,4-dioxane) to afford the target compounds in good to high yields. (C) 2011 Elsevier Ltd. All rights reserved.
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