1-(4-Chlorophenyl)-4-phenoxyphthalazine | 155937-29-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 1-(4-Chlorophenyl)-4-phenoxyphthalazine
• CAS: 155937-29-4
• 化学式: C₂₀H₁₃ClN₂O
• 分子量: 332.789
• InChiKey: CBAHDCFVEYVODF-UHFFFAOYSA-N

物化性质

• 沸点：
  534.6±40.0 °C(Predicted)
• 密度：
  1.290±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.3
• 重原子数：
  24
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  35
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-(4-Chlorophenyl)-4-phenoxyphthalazine 在 乙酸铵 作用下， 反应 0.5h， 以79%的产率得到4-(4-chloro-phenyl)-phthalazin-1-ylamine
  参考文献：
  名称：

  Synthesis and structure-activity relationships of 1-aminophthalazinium salts as GABAA receptor antagonists

  摘要：

  The synthesis and in vitro GABA(A) activity as GABA(A) antagonists of some 1-aminophthalazinium salts and imidazophthalazines are reported. Structure-activity relationships and a molecular, modelling study allowed us to define the features which determine receptor affinity within this class of compounds.

  DOI：

  10.1016/0223-5234(94)90205-4
• 作为产物：
  描述：

  1-chloro-4-(4-chlorophenyl)-phthalazine 、 苯酚 在 potassium carbonate 作用下， 反应 1.0h， 以88%的产率得到1-(4-Chlorophenyl)-4-phenoxyphthalazine
  参考文献：
  名称：

  Synthesis and structure-activity relationships of 1-aminophthalazinium salts as GABAA receptor antagonists

  摘要：

  The synthesis and in vitro GABA(A) activity as GABA(A) antagonists of some 1-aminophthalazinium salts and imidazophthalazines are reported. Structure-activity relationships and a molecular, modelling study allowed us to define the features which determine receptor affinity within this class of compounds.

  DOI：

  10.1016/0223-5234(94)90205-4

文献信息

• Synthesis and structure-activity relationships of 1-aminophthalazinium salts as GABAA receptor antagonists
  作者：V Colotta、L Cecchi、D Catarzi、G Filacchioni、A Galli、F Mori

  DOI：10.1016/0223-5234(94)90205-4

  日期：1994.1

  The synthesis and in vitro GABA(A) activity as GABA(A) antagonists of some 1-aminophthalazinium salts and imidazophthalazines are reported. Structure-activity relationships and a molecular, modelling study allowed us to define the features which determine receptor affinity within this class of compounds.