1-(4-hydroxyphenyl)octane-3-ol | 915316-43-7

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 1-(4-hydroxyphenyl)octane-3-ol
• 英文别名: 1-(4-Hydroxyphenyl)octan-3-ol；4-(3-hydroxyoctyl)phenol
• CAS: 915316-43-7
• 化学式: C₁₄H₂₂O₂
• 分子量: 222.327
• InChiKey: FWLIIIYRVCQIPM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  16
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  40.5
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-(4-hydroxyphenyl)octane-3-ol 在 氯化亚砜 、 potassium carbonate 、 N,N-二甲基甲酰胺 、 sodium iodide 作用下， 以 二氯甲烷 、 丙酮 为溶剂， 生成 1-[4-(4'-butoxybiphenyl-4-ylmethoxy)phenyl]-3-chlorooctane
  参考文献：
  名称：

  Synthesis of new liquid crystalline compounds with side chains containing hydroxy groups or chlorine atom

  摘要：

  Catalytic hydrogenation of the oxo group in 3-hydroxy-1-(4-hydroxyphenyl)octan-1-one gave 1-(4-hydroxyphenyl)octane-1.3-diol and 1-(4-hydroxyphenyl)octan-3-ol which were converted into the corresponding benzyl ethers containing a hydroxy group, 1.3-diol fragment, or chlorine atom in the side chain. The products were shown to possess liquid crystalline properties.

  DOI：

  10.1134/s1070428006030067
• 作为产物：
  描述：

  4-[(E)-(羟基亚胺)甲基]苯酚 在 palladium on activated charcoal 、 镍 N-氯代丁二酰亚胺 、 氢气 、 硼酸 、 三乙胺 作用下， 以 甲醇 为溶剂， 反应 2.0h， 生成 1-(4-hydroxyphenyl)octane-3-ol
  参考文献：
  名称：

  Synthesis of new liquid crystalline compounds with side chains containing hydroxy groups or chlorine atom

  摘要：

  Catalytic hydrogenation of the oxo group in 3-hydroxy-1-(4-hydroxyphenyl)octan-1-one gave 1-(4-hydroxyphenyl)octane-1.3-diol and 1-(4-hydroxyphenyl)octan-3-ol which were converted into the corresponding benzyl ethers containing a hydroxy group, 1.3-diol fragment, or chlorine atom in the side chain. The products were shown to possess liquid crystalline properties.

  DOI：

  10.1134/s1070428006030067

文献信息

• Synthesis of new liquid crystalline compounds with side chains containing hydroxy groups or chlorine atom
  作者：V. N. Kovganko、N. N. Kovganko

  DOI：10.1134/s1070428006030067

  日期：2006.3

  Catalytic hydrogenation of the oxo group in 3-hydroxy-1-(4-hydroxyphenyl)octan-1-one gave 1-(4-hydroxyphenyl)octane-1.3-diol and 1-(4-hydroxyphenyl)octan-3-ol which were converted into the corresponding benzyl ethers containing a hydroxy group, 1.3-diol fragment, or chlorine atom in the side chain. The products were shown to possess liquid crystalline properties.