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Diethylamino-ethenoxyimino-oxidoazanium | 143706-26-7

中文名称
——
中文别名
——
英文名称
Diethylamino-ethenoxyimino-oxidoazanium
英文别名
——
Diethylamino-ethenoxyimino-oxidoazanium化学式
CAS
143706-26-7
化学式
C6H13N3O2
mdl
——
分子量
159.188
InChiKey
PXBXWWPIODQCHK-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:
    197.0±23.0 °C(Predicted)
  • 密度:
    1.01±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    53.6
  • 氢给体数:
    0
  • 氢受体数:
    4

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

  • 作为产物:
    描述:
    2-Bromoethoxyimino-(diethylamino)-oxidoazanium2,8,9-三甲基-2,5,8,9-四氮杂-1-磷双环(3,3,3)十一烷乙腈 为溶剂, 以80%的产率得到Diethylamino-ethenoxyimino-oxidoazanium
    参考文献:
    名称:
    Improved synthesis of V-PYRRO/NO, a liver-selective nitric oxide prodrug, and analogues
    摘要:
    The reported synthesis of O-2-vinyl 1-(pyrrolidin-1-yl)diazen-1-ium-1,2-diolate(V-PYRRO/NO), a hepatoprotective agent, was cumbersome and limited by a poor overall yield of 4% from sodium 1-(pyrrolidin-1-yl)diazen-1-ium-1,2-diolate (PYRRO/No). We report an improved synthesis of V-PYRRO/NO in two steps with a significantly higher overall yield of 40% from PYRRO/NO. Using this protocol, a number of structural analogues of V-PYRRO/NO were prepared in good yields. Published by Elsevier Ltd.
    DOI:
    10.1016/j.tetlet.2009.02.103
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文献信息

  • Improved synthesis of V-PYRRO/NO, a liver-selective nitric oxide prodrug, and analogues
    作者:Sam Y. Hong、Joseph E. Saavedra、Larry K. Keefer、Harinath Chakrapani
    DOI:10.1016/j.tetlet.2009.02.103
    日期:2009.5
    The reported synthesis of O-2-vinyl 1-(pyrrolidin-1-yl)diazen-1-ium-1,2-diolate(V-PYRRO/NO), a hepatoprotective agent, was cumbersome and limited by a poor overall yield of 4% from sodium 1-(pyrrolidin-1-yl)diazen-1-ium-1,2-diolate (PYRRO/No). We report an improved synthesis of V-PYRRO/NO in two steps with a significantly higher overall yield of 40% from PYRRO/NO. Using this protocol, a number of structural analogues of V-PYRRO/NO were prepared in good yields. Published by Elsevier Ltd.
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