10-(4-(bis(2-(((benzyloxy)carbonyl)amino)ethyl)amino)butyl)-5,5-difluoro-1,3,7,9-tetramethyl-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium | 1245573-65-2

• 英文名称: 10-(4-(bis(2-(((benzyloxy)carbonyl)amino)ethyl)amino)butyl)-5,5-difluoro-1,3,7,9-tetramethyl-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium
• CAS: 1245573-65-2
• 化学式: C₃₇H₄₆BF₂N₅O₄
• 分子量: 673.611
• InChiKey: YZARVDDUZGRXKM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
  None
• 环数：
  None
• sp3杂化的碳原子比例：
  None
• 拓扑面积：
  None
• 氢给体数：
  None
• 氢受体数：
  None

反应信息

• 作为反应物：
  描述：

  10-(4-(bis(2-(((benzyloxy)carbonyl)amino)ethyl)amino)butyl)-5,5-difluoro-1,3,7,9-tetramethyl-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium 在 1,4-环己二烯 、 palladium on carbon 作用下， 以 乙醇 为溶剂， 以96%的产率得到
  参考文献：
  名称：

  Single-Molecule Imaging of Platinum Ligand Exchange Reaction Reveals Reactivity Distribution

  摘要：

  Single-molecule fluorescence microscopy provided information about the real-time distribution of chemical reactivity on silicon oxide supports at the solution surface interface, at a level of detail which would be unavailable from a traditional ensemble technique or from a technique that imaged the static physical properties of the surface. Chemical reactions on the surface were found to be uncorrelated; that is, the chemical reaction of one metal complex did not influence the location of a future chemical reaction of another metal complex.

  DOI：

  10.1021/ja105517d
• 作为产物：
  描述：

  10-(4-chlorobutyl)-5,5-difluoro-1,3,7,9-tetramethyl-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium 、 、 N,N″-二-Z-二亚乙基三胺 在 potassium carbonate 、 sodium iodide 作用下， 以 丙酮 为溶剂， 反应 96.0h， 以72%的产率得到10-(4-(bis(2-(((benzyloxy)carbonyl)amino)ethyl)amino)butyl)-5,5-difluoro-1,3,7,9-tetramethyl-5H-5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium
  参考文献：
  名称：

  Single-Molecule Imaging of Platinum Ligand Exchange Reaction Reveals Reactivity Distribution

  摘要：

  Single-molecule fluorescence microscopy provided information about the real-time distribution of chemical reactivity on silicon oxide supports at the solution surface interface, at a level of detail which would be unavailable from a traditional ensemble technique or from a technique that imaged the static physical properties of the surface. Chemical reactions on the surface were found to be uncorrelated; that is, the chemical reaction of one metal complex did not influence the location of a future chemical reaction of another metal complex.

  DOI：

  10.1021/ja105517d