| 89638-93-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• CAS: 89638-93-7；89707-91-5
• 化学式: C₁₆H₂₀O₃
• 分子量: 260.333
• InChiKey: VOWYXUADQQTLOW-KMQIDDJNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.71
• 重原子数：
  19.0
• 可旋转键数：
  3.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  41.99
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  3,4-二甲氧基苯乙胺 、 以 乙醇 为溶剂， 反应 3.5h， 生成
  参考文献：
  名称：

  Synthesis of a novel series of (aryloxy)propanolamines: new selective .beta.2-blocking agents

  摘要：

  A new family of beta-blocking drugs is described. The originality of the new molecules lies in their functionalized hydrophobic folded structure, the basic part of which contains a benzocyclobutene ring. Excellent beta 2-blocker selectivity has been obtained with some of these compounds. Interestingly, this selectivity was not modified toward beta 1-blocker activity by introduction of the usual beta 1 inducer groups.

  DOI：

  10.1021/jm00372a016
• 作为产物：
  描述：

  3-氯苯酚 在 吡啶 、 sodium hydroxide 、 lithium aluminium tetrahydride 、 sodium amide 、 sodium t-butanolate 作用下， 以 乙醚 、 丙酮 为溶剂， 反应 3.0h， 生成
  参考文献：
  名称：

  Synthesis of a novel series of (aryloxy)propanolamines: new selective .beta.2-blocking agents

  摘要：

  A new family of beta-blocking drugs is described. The originality of the new molecules lies in their functionalized hydrophobic folded structure, the basic part of which contains a benzocyclobutene ring. Excellent beta 2-blocker selectivity has been obtained with some of these compounds. Interestingly, this selectivity was not modified toward beta 1-blocker activity by introduction of the usual beta 1 inducer groups.

  DOI：

  10.1021/jm00372a016