(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)2SnPh2 | 96325-94-9

• 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: (3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)2SnPh2
• CAS: 96325-94-9
• 化学式: C₂₈H₁₈F₂₆Sn
• 分子量: 967.119
• InChiKey: LCDGWDJILOLYNC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  11.51
• 重原子数：
  55
• 可旋转键数：
  16
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  26

反应信息

• 作为反应物：
  描述：

  (3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)2SnPh2 在 溴 作用下， 以 甲醇 为溶剂， 生成 (3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)2SnBr2
  参考文献：
  名称：

  Synthesis, Characterisation and Anti-Tumour Activity of Bis(Polyfluoroalkyl)Tin Dihalides

  摘要：

  AbstractThe synthesis and characterisation of fifteen new organotin compounds containing at least two CF3(CF2)5CH2‐CH2 groups bound to tin are described. The activity of six of these compounds towards the murine P388 lymphocytic leukaemia tumour is given.

  DOI：

  10.1002/bscb.19840931209
• 作为产物：
  描述：

  二苯基二氯化锡 、 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl magnesium iodide 以 乙醚 为溶剂， 生成 (3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)2SnPh2
  参考文献：
  名称：

  Synthesis, Characterisation and Anti-Tumour Activity of Bis(Polyfluoroalkyl)Tin Dihalides

  摘要：

  AbstractThe synthesis and characterisation of fifteen new organotin compounds containing at least two CF3(CF2)5CH2‐CH2 groups bound to tin are described. The activity of six of these compounds towards the murine P388 lymphocytic leukaemia tumour is given.

  DOI：

  10.1002/bscb.19840931209

文献信息

• DE, CLERCQ, L.;WILLEM, R.;GIELEN, M.;ATASSI, G., BULL. SOC. CHIM. BELG., 1984, 93, N 12, 1089-1097
  作者：DE, CLERCQ, L.、WILLEM, R.、GIELEN, M.、ATASSI, G.

  DOI：——

  日期：——
• Synthesis, Characterisation and Anti-Tumour Activity of Bis(Polyfluoroalkyl)Tin Dihalides
  作者：Ludo De Clercq、Rudolph Willem、Marcel Gielen、Ghanem Atassi

  DOI：10.1002/bscb.19840931209

  日期：——

  AbstractThe synthesis and characterisation of fifteen new organotin compounds containing at least two CF3(CF2)5CH2‐CH2 groups bound to tin are described. The activity of six of these compounds towards the murine P388 lymphocytic leukaemia tumour is given.