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1-(Propan-2-ylamino)-3-(2-prop-2-enylphenoxy)butan-2-ol | 78711-15-6

中文名称
——
中文别名
——
英文名称
1-(Propan-2-ylamino)-3-(2-prop-2-enylphenoxy)butan-2-ol
英文别名
——
1-(Propan-2-ylamino)-3-(2-prop-2-enylphenoxy)butan-2-ol化学式
CAS
78711-15-6
化学式
C16H25NO2
mdl
——
分子量
263.38
InChiKey
LAEITBINOLJTJP-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):
    3.1
  • 重原子数:
    19
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    41.5
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2-烯丙基酚三氟化硼乙醚 作用下, 以 乙醇 为溶剂, 反应 44.0h, 生成 1-(Propan-2-ylamino)-3-(2-prop-2-enylphenoxy)butan-2-ol
    参考文献:
    名称:
    .beta.-Adrenergic blocking agents. .alpha.- and .gamma.-Methyl(aryloxy)propanolamines
    摘要:
    A series of gamma-methyl- (5) and alpha-methyl(aryloxy)propanolamines (6) were synthesized and evaluated for beta-adrenergic blocking action. The binding constant (KD) was determined for compounds 5a-j on cultured C6-2B astrocytoma cells. Compounds 5a-j and 6a-e were evaluated for beta 1-antagonist action on guinea pig atria and beta 2-antagonist action on guinea pig tracheal strips. Several gamma-methyl(aryloxy)propanolamines showed affinity for beta receptors and a possible preference for beta 2 receptors.
    DOI:
    10.1021/jm00142a017
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文献信息

  • .beta.-Adrenergic blocking agents. .alpha.- and .gamma.-Methyl(aryloxy)propanolamines
    作者:Thomas L. Lemke、Michael B. Cramer、Stanley W. Adamski、Carolyn A. Pedone、Gary Brooker
    DOI:10.1021/jm00142a017
    日期:1981.10
    A series of gamma-methyl- (5) and alpha-methyl(aryloxy)propanolamines (6) were synthesized and evaluated for beta-adrenergic blocking action. The binding constant (KD) was determined for compounds 5a-j on cultured C6-2B astrocytoma cells. Compounds 5a-j and 6a-e were evaluated for beta 1-antagonist action on guinea pig atria and beta 2-antagonist action on guinea pig tracheal strips. Several gamma-methyl(aryloxy)propanolamines showed affinity for beta receptors and a possible preference for beta 2 receptors.
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