N5,N5,N9,N9-tetraethyl-4,6,8,10-tetraoxa-5,9-diphospha-1,3(1,2)-dinaphthalena-7(1,3)-benzenacyclodecaphane-5,9-diamine | 1252583-03-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: N5,N5,N9,N9-tetraethyl-4,6,8,10-tetraoxa-5,9-diphospha-1,3(1,2)-dinaphthalena-7(1,3)-benzenacyclodecaphane-5,9-diamine
• CAS: 1252583-03-1
• 化学式: C₃₅H₃₈N₂O₄P₂
• 分子量: 612.645
• InChiKey: FNBRJZQGEJIPKW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  9.95
• 重原子数：
  43.0
• 可旋转键数：
  6.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  43.4
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  N5,N5,N9,N9-tetraethyl-4,6,8,10-tetraoxa-5,9-diphospha-1,3(1,2)-dinaphthalena-7(1,3)-benzenacyclodecaphane-5,9-diamine 在 sulfur 作用下， 以 二氯甲烷 为溶剂， 反应 48.0h， 以30%的产率得到5,9-bis(diethylamino)-4,6,8,10-tetraoxa-5,9-diphospha-1,3(1,2)-dinaphthalena-7(1,3)-benzenacyclodecaphane 5,9-disulfide
  参考文献：
  名称：

  Phosphomacrocyclic systems based on 2,2′-dihydroxy-1,1′-dinaphtylmethane

  摘要：

  For the first time phosphomacrocyclic systems were synthesized based on 2,2'-dihydroxy-1,1'-dinaphthylmethane, other aromatic diols, and phosphorous hexaethyltriamide. Spontaneous transformation of the obtained macrocycles into the more stable 1,3,2-dioxaphosphacyn and cyclobisamidophosphite was established.

  DOI：

  10.1134/s1070363210050099
• 作为产物：
  描述：

  间苯二酚 以 1,4-二氧六环 、 乙腈 为溶剂， 反应 78.0h， 生成 N5,N5,N9,N9-tetraethyl-4,6,8,10-tetraoxa-5,9-diphospha-1,3(1,2)-dinaphthalena-7(1,3)-benzenacyclodecaphane-5,9-diamine
  参考文献：
  名称：

  Phosphomacrocyclic systems based on 2,2′-dihydroxy-1,1′-dinaphtylmethane

  摘要：

  For the first time phosphomacrocyclic systems were synthesized based on 2,2'-dihydroxy-1,1'-dinaphthylmethane, other aromatic diols, and phosphorous hexaethyltriamide. Spontaneous transformation of the obtained macrocycles into the more stable 1,3,2-dioxaphosphacyn and cyclobisamidophosphite was established.

  DOI：

  10.1134/s1070363210050099