Diethyl 2,5-bis(2-ethoxycarbonylanilino)benzene-1,4-dicarboxylate | 1233390-61-8

• 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: Diethyl 2,5-bis(2-ethoxycarbonylanilino)benzene-1,4-dicarboxylate
• 英文别名: diethyl 2,5-bis(2-ethoxycarbonylanilino)benzene-1,4-dicarboxylate
• CAS: 1233390-61-8
• 化学式: C₃₀H₃₂N₂O₈
• 分子量: 548.593
• InChiKey: DDMPTOOZXGRAGR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7
• 重原子数：
  40
• 可旋转键数：
  16
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  129
• 氢给体数：
  2
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  Diethyl 2,5-bis(2-ethoxycarbonylanilino)benzene-1,4-dicarboxylate 在 lead(IV) tetraacetate 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 以100%的产率得到C₃₀H₃₀N₂O₈
  参考文献：
  名称：

  Luminescent properties of phenylenediamine derivatives depending on the redox states

  摘要：

  Phenylenediamines bearing the ethoxycarbonyl groups were synthesized to modulate luminescent properties. Switching of the luminescent properties was achieved by redox change between the phenylenediamine and quinonediimine derivatives. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2010.04.028
• 作为产物：
  描述：

  C₃₀H₃₀N₂O₈ 在 一水合肼 作用下， 反应 30.0h， 以88%的产率得到Diethyl 2,5-bis(2-ethoxycarbonylanilino)benzene-1,4-dicarboxylate
  参考文献：
  名称：

  Luminescent properties of phenylenediamine derivatives depending on the redox states

  摘要：

  Phenylenediamines bearing the ethoxycarbonyl groups were synthesized to modulate luminescent properties. Switching of the luminescent properties was achieved by redox change between the phenylenediamine and quinonediimine derivatives. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2010.04.028

文献信息

• Luminescent properties of phenylenediamine derivatives depending on the redox states
  作者：Satoshi D. Ohmura、Toshiyuki Moriuchi、Toshikazu Hirao

  DOI：10.1016/j.tetlet.2010.04.028

  日期：2010.6

  Phenylenediamines bearing the ethoxycarbonyl groups were synthesized to modulate luminescent properties. Switching of the luminescent properties was achieved by redox change between the phenylenediamine and quinonediimine derivatives. (C) 2010 Elsevier Ltd. All rights reserved.