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2-(4-Methoxyphenyl)-3-pyridin-3-ylprop-2-enenitrile

中文名称
——
中文别名
——
英文名称
2-(4-Methoxyphenyl)-3-pyridin-3-ylprop-2-enenitrile
英文别名
——
2-(4-Methoxyphenyl)-3-pyridin-3-ylprop-2-enenitrile化学式
CAS
——
化学式
C15H12N2O
mdl
——
分子量
236.273
InChiKey
RQWSCDRFGHLEGJ-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):
    2.6
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    45.9
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-(4-Methoxyphenyl)-3-pyridin-3-ylprop-2-enenitrile 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 生成 2-(4-Methoxyphenyl)-3-pyridin-3-ylpropanenitrile
    参考文献:
    名称:
    Heteroaryl β-tetralin ureas as novel antagonists of human TRPV1
    摘要:
    We report on a series of alpha-substituted-beta-tetralin-derived and related phenethyl-based isoquinolinyl and hydroxynaphthyl ureas as potent antagonists of the human TRPV1 receptor. The synthesis and Structure-activity relationships (SAR) of the series are described. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.09.036
  • 作为产物:
    参考文献:
    名称:
    Heteroaryl β-tetralin ureas as novel antagonists of human TRPV1
    摘要:
    We report on a series of alpha-substituted-beta-tetralin-derived and related phenethyl-based isoquinolinyl and hydroxynaphthyl ureas as potent antagonists of the human TRPV1 receptor. The synthesis and Structure-activity relationships (SAR) of the series are described. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.09.036
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文献信息

  • Heteroaryl β-tetralin ureas as novel antagonists of human TRPV1
    作者:Michele C. Jetter、Mark A. Youngman、James J. McNally、Mark E. McDonnell、Sui-Po Zhang、Adrienne E. Dubin、Nadia Nasser、Ellen E. Codd、Christopher M. Flores、Scott L. Dax
    DOI:10.1016/j.bmcl.2007.09.036
    日期:2007.11
    We report on a series of alpha-substituted-beta-tetralin-derived and related phenethyl-based isoquinolinyl and hydroxynaphthyl ureas as potent antagonists of the human TRPV1 receptor. The synthesis and Structure-activity relationships (SAR) of the series are described. (C) 2007 Elsevier Ltd. All rights reserved.
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