2,4-Dichloro-6-(2-phenylmethoxyethoxy)-1,3,5-triazine | 1016892-60-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2,4-Dichloro-6-(2-phenylmethoxyethoxy)-1,3,5-triazine
• 英文别名: 2,4-dichloro-6-(2-phenylmethoxyethoxy)-1,3,5-triazine
• CAS: 1016892-60-6
• 化学式: C₁₂H₁₁Cl₂N₃O₂
• 分子量: 300.144
• InChiKey: HRCWATQLUSWBIC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  19
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  57.1
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  [(3S,4S)-4-(dodecylcarbamoyloxy)pyrrolidin-3-yl] N-dodecylcarbamate 、 2,4-Dichloro-6-(2-phenylmethoxyethoxy)-1,3,5-triazine 在 N,N-二异丙基乙胺 作用下， 以 甲苯 为溶剂， 反应 0.25h， 以34%的产率得到[(3S,4S)-1-[4-[(3S,4S)-3,4-bis(dodecylcarbamoyloxy)pyrrolidin-1-yl]-6-(2-phenylmethoxyethoxy)-1,3,5-triazin-2-yl]-4-(dodecylcarbamoyloxy)pyrrolidin-3-yl] N-dodecylcarbamate
  参考文献：
  名称：

  The triazine ring as a scaffold for the synthesis of new organogelators

  摘要：

  The synthesis of new organogelators based on a triazine nucleus is described together with the analysis of the properties of the main compound 15. This compound revealed an efficient organogelator in both polar and apolar solvents and represents a promising precursor of other functionalized organogelators. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2007.12.124
• 作为产物：
  描述：

  三聚氯氰 、 2-苄氧基乙醇 在 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 为溶剂， 反应 60.0h， 以49%的产率得到2,4-Dichloro-6-(2-phenylmethoxyethoxy)-1,3,5-triazine
  参考文献：
  名称：

  The triazine ring as a scaffold for the synthesis of new organogelators

  摘要：

  The synthesis of new organogelators based on a triazine nucleus is described together with the analysis of the properties of the main compound 15. This compound revealed an efficient organogelator in both polar and apolar solvents and represents a promising precursor of other functionalized organogelators. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2007.12.124

文献信息

• The triazine ring as a scaffold for the synthesis of new organogelators
  作者：Stefano Cicchi、Giacomo Ghini、Sara Fallani、Alberto Brandi、Debora Berti、Francesca Betti、Piero Baglioni

  DOI：10.1016/j.tetlet.2007.12.124

  日期：2008.3

  The synthesis of new organogelators based on a triazine nucleus is described together with the analysis of the properties of the main compound 15. This compound revealed an efficient organogelator in both polar and apolar solvents and represents a promising precursor of other functionalized organogelators. (c) 2008 Elsevier Ltd. All rights reserved.