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1-isopropylaminomethyl-2-naphthol | 95768-31-3

中文名称
——
中文别名
——
英文名称
1-isopropylaminomethyl-2-naphthol
英文别名
1-Isopropylaminomethyl-naphthol-(2);1-{[(Propan-2-yl)amino]methyl}naphthalen-2-ol;1-[(propan-2-ylamino)methyl]naphthalen-2-ol
1-isopropylaminomethyl-2-naphthol化学式
CAS
95768-31-3
化学式
C14H17NO
mdl
MFCD02600422
分子量
215.295
InChiKey
ZPMDMMJMLQAGQD-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:
    360.3±17.0 °C(Predicted)
  • 密度:
    1.092±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.285
  • 拓扑面积:
    32.3
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2-Isopropyl-2.3-dihydro-1H-naphth<1.2-e>-1.3-oxazin 生成 1-isopropylaminomethyl-2-naphthol
    参考文献:
    名称:
    Synthesis and Study of Mannich Bases from 2-Naphthol and Primary Amines1
    摘要:
    DOI:
    10.1021/jo01025a038
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文献信息

  • Synthesis and cardiovascular evaluation of N-substituted 1-aminomethyl-2-naphthols
    作者:A Shen
    DOI:10.1016/s0223-5234(99)00204-4
    日期:1999.10
    A series of 1-alkylaminomethylnaphthols have been prepared. These compounds were readily prepared in good yields by addition of 2-naphthol to formalin and alkylamines. The hypotensive and bradycardiac effects of these compounds in normotensive rats as well as their in vitro inotropic and aortic contraction effects in isolated rat left atria and aorta have been evaluated. A higher depressor and bradycardiac activity was found for compounds substituted on nitrogen by naphthol with primary amines, i.e., ethylamine, propylamine, isopropylamine, or butylamine and with a cyclic secondary amine, i.e., pyrrolidinyl. These compounds produced biphasic changes in contractile force in isolated rat atria which was correlated to blood pressure and heart rate activity. 1-Isopropylaminomethyl-2-naphthol hydrochloride relaxed isolated rat aortic rings precontracted with high extracellular K+ (80 mM) and Ca2+ (1.9 mM). The suppressive effects of the compounds may involve a direct inhibition of Ca2+ channels. The biological activity of these compounds can be explained in terms of substitution on nitrogen. (C) 1999 Editions scientifiques et medicales Elsevier SAS.
  • Synthesis and Study of Mannich Bases from 2-Naphthol and Primary Amines<sup>1</sup>
    作者:William J. Burke、Wilmonte A. Nasutavicus、Carl Weatherbee
    DOI:10.1021/jo01025a038
    日期:1964.2
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