13,24,38,53-Tetra(tricosan-12-yl)-13,24,38,53-tetrazaheptadecacyclo[45.7.1.17,11.126,30.136,40.03,46.04,33.06,31.08,29.09,18.010,15.019,28.022,27.034,45.043,48.051,55.044,56]octapentaconta-1,3(46),4,6,8,10(15),11(58),16,18,20,22(27),26(57),28,30,32,34(45),35,40(56),41,43,47,49,51(55)-tricosaene-12,14,23,25,37,39,52,54-octone | 1224849-49-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 芘
• 英文名称: 13,24,38,53-Tetra(tricosan-12-yl)-13,24,38,53-tetrazaheptadecacyclo[45.7.1.17,11.126,30.136,40.03,46.04,33.06,31.08,29.09,18.010,15.019,28.022,27.034,45.043,48.051,55.044,56]octapentaconta-1,3(46),4,6,8,10(15),11(58),16,18,20,22(27),26(57),28,30,32,34(45),35,40(56),41,43,47,49,51(55)-tricosaene-12,14,23,25,37,39,52,54-octone
• 英文别名: 13,24,38,53-tetra(tricosan-12-yl)-13,24,38,53-tetrazaheptadecacyclo[45.7.1.17,11.126,30.136,40.03,46.04,33.06,31.08,29.09,18.010,15.019,28.022,27.034,45.043,48.051,55.044,56]octapentaconta-1,3(46),4,6,8,10(15),11(58),16,18,20,22(27),26(57),28,30,32,34(45),35,40(56),41,43,47,49,51(55)-tricosaene-12,14,23,25,37,39,52,54-octone
• CAS: 1224849-49-3
• 化学式: C₁₄₆H₂₀₂N₄O₈
• 分子量: 2141.23
• InChiKey: OWIIQXBTXRKKND-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  55.2
• 重原子数：
  158
• 可旋转键数：
  84
• 环数：
  17.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  150
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  、 12-tricosanamine 在 咪唑 作用下， 反应 6.0h， 以100%的产率得到13,24,38,53-Tetra(tricosan-12-yl)-13,24,38,53-tetrazaheptadecacyclo[45.7.1.17,11.126,30.136,40.03,46.04,33.06,31.08,29.09,18.010,15.019,28.022,27.034,45.043,48.051,55.044,56]octapentaconta-1,3(46),4,6,8,10(15),11(58),16,18,20,22(27),26(57),28,30,32,34(45),35,40(56),41,43,47,49,51(55)-tricosaene-12,14,23,25,37,39,52,54-octone
  参考文献：
  名称：

  sim双酰亚胺的平面共轭梯形低聚物的设计概念和通过区域选择性光环化的有效合成策略。

  摘要：

  通过光环化，将苯，噻吩并[3,2-b]噻吩和芴单元嵌入两个per单元之间。对称的低聚per双酰亚胺6具有广泛的吸收能力和较强的电子接受能力。

  DOI：

  10.1039/b925605a