5-Hexylnaphthalen-1-ol | 873426-03-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 5-Hexylnaphthalen-1-ol
• 英文别名: 5-hexylnaphthalen-1-ol
• CAS: 873426-03-0
• 化学式: C₁₆H₂₀O
• 分子量: 228.334
• InChiKey: DAQPNDOWDLMJOH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.8
• 重原子数：
  17
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  5-Hexylnaphthalen-1-ol 在 palladium on activated charcoal 盐酸 、 氢气 、 丙酸 、 苯硼酸 作用下， 以 四氢呋喃 、 甲醇 、 苯 为溶剂， 生成 5-Hexyl-2-methylnaphthalen-1-ol
  参考文献：
  名称：

  The structure–activity relationships of mansonone F, a potent anti-MRSA sesquiterpenoid quinone: SAR studies on the C6 and C9 analogs

  摘要：

  For the systematic SAR study on mansonone F, a series of C6 and C9 analogs of mansonone F have been synthesized and their anti-MRSA activities were evaluated. Most of the analogs exhibited good or excellent anti-MRSA activities. In particular, the 6-n-butylmansonone F showed fourfold higher antibacterial activities compared to that of vancomycin. (c) 2005 Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmcl.2005.09.024
• 作为产物：
  描述：

  在 palladium on activated charcoal 、 三溴化硼 作用下， 以 三甘醇二甲醚 、 二氯甲烷 为溶剂， 生成 5-Hexylnaphthalen-1-ol
  参考文献：
  名称：

  The structure–activity relationships of mansonone F, a potent anti-MRSA sesquiterpenoid quinone: SAR studies on the C6 and C9 analogs

  摘要：

  For the systematic SAR study on mansonone F, a series of C6 and C9 analogs of mansonone F have been synthesized and their anti-MRSA activities were evaluated. Most of the analogs exhibited good or excellent anti-MRSA activities. In particular, the 6-n-butylmansonone F showed fourfold higher antibacterial activities compared to that of vancomycin. (c) 2005 Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmcl.2005.09.024

文献信息

• The structure–activity relationships of mansonone F, a potent anti-MRSA sesquiterpenoid quinone: SAR studies on the C6 and C9 analogs
  作者：Young-Ger Suh、Sun Nam Kim、Dong-Yun Shin、Soon-Sil Hyun、Do-Sang Lee、Kyung-Hoon Min、Sae Mi Han、Funan Li、Eung-Chil Choi、Seong-Hak Choi

  DOI：10.1016/j.bmcl.2005.09.024

  日期：2006.1

  For the systematic SAR study on mansonone F, a series of C6 and C9 analogs of mansonone F have been synthesized and their anti-MRSA activities were evaluated. Most of the analogs exhibited good or excellent anti-MRSA activities. In particular, the 6-n-butylmansonone F showed fourfold higher antibacterial activities compared to that of vancomycin. (c) 2005 Published by Elsevier Ltd.