6-piperidinomethyl-2-propenylphenol | 1086558-11-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 6-piperidinomethyl-2-propenylphenol
• 英文别名: 2-(piperidin-1-ylmethyl)-6-prop-1-enylphenol
• CAS: 1086558-11-3
• 化学式: C₁₅H₂₁NO
• 分子量: 231.338
• InChiKey: RLUGFMWYJIMROE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  23.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  6-piperidinomethyl-2-propenylphenol 、 3-溴丙炔 在 potassium hydroxide 作用下， 以 异丙醇 为溶剂， 以77.6 %的产率得到1-propenyl-2-propargyloxy-3-piperidinomethylbenzene
  参考文献：
  名称：

  Synthesis and Study of 1-Alkenyl-2-propargyloxy-3-aminomethylbenzenes as Acid Corrosion Inhibitors and Antimicrobial Additives to Cutting Fluids

  摘要：

  DOI：

  10.1134/s1070427220110026
• 作为产物：
  描述：

  哌啶 以 水 为溶剂， 生成 6-piperidinomethyl-2-propenylphenol
  参考文献：
  名称：

  Synthesis and Study of 1-Alkenyl-2-propargyloxy-3-aminomethylbenzenes as Acid Corrosion Inhibitors and Antimicrobial Additives to Cutting Fluids

  摘要：

  DOI：

  10.1134/s1070427220110026

文献信息

• Aminomethylated derivatives of 2-propenyl- and 4-isopropenylphenols as antimicrobial additives for petroleum products
  作者：M. R. Bairamov、A. M. Magerramov、G. M. Mekhtieva、R. A. Abushev、M. A. Agaeva、S. A. Gasanova、I. G. Mamedov

  DOI：10.1134/s096554411001010x

  日期：2010.1

  A number of aminomethylated derivatives of 2-propenyl-, 4-isopropenylphenols have been synthesized and their antimicrobial properties have been studied in M-12 engine oil and TS-1 jet fuel (at concentrations of 1-2% and 0.3-0.5%, respectively). They have been found to possess bactericidal and fungicidal properties and significantly improve the antimicrobial properties of both of the materials (as compared to the well-known antimicrobial additive, 8-hydroxyquinoline). The presence of an alkenyl substituent along with an aminomethyl group in the structure of the substances in question has been demonstrated to enhance the antimicrobial properties. The formation of an intermolecular and intramolecular hydrogen bond in the initial and synthesized phenolic compounds has been studied.