1-(2,2-Dimethoxyethyl)-3-(2,6-dimethylphenyl)urea | 1024398-99-9

• 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: 1-(2,2-Dimethoxyethyl)-3-(2,6-dimethylphenyl)urea
• CAS: 1024398-99-9
• 化学式: C₁₃H₂₀N₂O₃
• 分子量: 252.313
• InChiKey: XTICPXSDEMLHGB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  18
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  59.6
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-(2,2-Dimethoxyethyl)-3-(2,6-dimethylphenyl)urea 在 盐酸 作用下， 生成 1-(2,6-dimethylphenyl)-2-imidazolone
  参考文献：
  名称：

  Zirconium Complexes Supported by Imidazolones: Synthesis, Characterization, and Application of Precatalysts for the Hydroamination of Aminoalkenes

  摘要：

  Dimeric zirconium benzyl and amide complexes supported by an imidazolone framework have been successfully synthesized and fully characterized. The amide complexes were found to be effective catalysts for intramolecular hydroamination of primary and secondary amines.

  DOI：

  10.1021/om100296m
• 作为产物：
  描述：

  氨基乙醛缩二甲醇 、 2,6-二甲苯基异氰酸酯 生成 1-(2,2-Dimethoxyethyl)-3-(2,6-dimethylphenyl)urea
  参考文献：
  名称：

  Zirconium Complexes Supported by Imidazolones: Synthesis, Characterization, and Application of Precatalysts for the Hydroamination of Aminoalkenes

  摘要：

  Dimeric zirconium benzyl and amide complexes supported by an imidazolone framework have been successfully synthesized and fully characterized. The amide complexes were found to be effective catalysts for intramolecular hydroamination of primary and secondary amines.

  DOI：

  10.1021/om100296m

文献信息

• Zirconium Complexes Supported by Imidazolones: Synthesis, Characterization, and Application of Precatalysts for the Hydroamination of Aminoalkenes
  作者：Yu-Cheng Hu、Cheng-Feng Liang、Jie-Hong Tsai、Glenn P. A. Yap、Ya-Ting Chang、Tiow-Gan Ong

  DOI：10.1021/om100296m

  日期：2010.8.9

  Dimeric zirconium benzyl and amide complexes supported by an imidazolone framework have been successfully synthesized and fully characterized. The amide complexes were found to be effective catalysts for intramolecular hydroamination of primary and secondary amines.