1-Naphthalen-1-yl-2-[1,2,4]triazol-1-yl-ethanol | 161878-59-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 1-Naphthalen-1-yl-2-[1,2,4]triazol-1-yl-ethanol
• 英文别名: 1-Naphthalen-1-yl-2-(1,2,4-triazol-1-yl)ethanol
• CAS: 161878-59-7
• 化学式: C₁₄H₁₃N₃O
• mdl: MFCD16236116
• 分子量: 239.277
• InChiKey: IAJVHDVNRXMKOZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.142
• 拓扑面积：
  50.9
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2,4-二氯氯苄 、 1-Naphthalen-1-yl-2-[1,2,4]triazol-1-yl-ethanol 在 sodium hydride 作用下， 生成 1-[2-(2,4-Dichloro-benzyloxy)-2-naphthalen-1-yl-ethyl]-1H-[1,2,4]triazole
  参考文献：
  名称：

  Aromatic ethers of 1-aryl 2-(1H-azolyl)ethanol: study of antifungal activity

  摘要：

  Aromatic ethers related to antifungal azole miconazole were synthesized and tested against various strains of Candida. We found that activity is related to the nature of the aromatic ring and the position of substituents on this ring. Activity is more strongly dependent on the substituent in the 2 position of the ethyl chain than on the aromatic group linked through the oxygen. Triazoles were always less potent than the corresponding imidazole analogues.

  DOI：

  10.1016/0223-5234(96)88315-2
• 作为产物：
  描述：

  1-(1-naphthalenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone 在 sodium tetrahydroborate 作用下， 以 甲醇 为溶剂， 反应 2.0h， 以69%的产率得到1-Naphthalen-1-yl-2-[1,2,4]triazol-1-yl-ethanol
  参考文献：
  名称：

  Aromatic ethers of 1-aryl 2-(1H-azolyl)ethanol: study of antifungal activity

  摘要：

  Aromatic ethers related to antifungal azole miconazole were synthesized and tested against various strains of Candida. We found that activity is related to the nature of the aromatic ring and the position of substituents on this ring. Activity is more strongly dependent on the substituent in the 2 position of the ethyl chain than on the aromatic group linked through the oxygen. Triazoles were always less potent than the corresponding imidazole analogues.

  DOI：

  10.1016/0223-5234(96)88315-2