2-[[3-[3-Hydroxy-2,2-bis(hydroxymethyl)propoxy]-2-[[3-[3-[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]-2,2-bis[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]-2,2-bis[[3-[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]-2,2-bis[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]methyl]propoxy]methyl]-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol | 110614-85-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-[[3-[3-Hydroxy-2,2-bis(hydroxymethyl)propoxy]-2-[[3-[3-[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]-2,2-bis[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]-2,2-bis[[3-[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]-2,2-bis[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]methyl]propoxy]methyl]-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol
• CAS: 110614-85-2
• 化学式: C₈₅H₁₇₂O₅₂
• 分子量: 2026.27
• InChiKey: FZZRWENJIKLNAM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -24.8
• 重原子数：
  137
• 可旋转键数：
  100
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  876
• 氢给体数：
  36
• 氢受体数：
  52

反应信息

• 作为反应物：
  描述：

  2-[[3-[3-Hydroxy-2,2-bis(hydroxymethyl)propoxy]-2-[[3-[3-[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]-2,2-bis[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]-2,2-bis[[3-[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]-2,2-bis[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]methyl]propoxy]methyl]-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol 、 对甲苯磺酰氯 、 溴化钠 生成 1,3-bis[3-[3-bromo-2,2-bis(bromomethyl)propoxy]-2,2-bis[[3-bromo-2,2-bis(bromomethyl)propoxy]methyl]propoxy]-2,2-bis[[3-[3-bromo-2,2-bis(bromomethyl)propoxy]-2,2-bis[[3-bromo-2,2-bis(bromomethyl)propoxy]methyl]propoxy]methyl]propane
  参考文献：
  名称：

  PADIAS, ANNE BUYLE;HALL, H. K., JR.;TOMALIA, DONALD A.;MCCONNELL, J. R., J. ORG. CHEM., 52,(1987) N 24, 5305-5312

  摘要：

  DOI：
• 作为产物：
  描述：

  4-[[3-(2,6,7-trioxabicyclo[2.2.2]octan-4-ylmethoxy)-2-[[3-[3-(2,6,7-trioxabicyclo[2.2.2]octan-4-ylmethoxy)-2,2-bis(2,6,7-trioxabicyclo[2.2.2]octan-4-ylmethoxymethyl)propoxy]-2,2-bis[[3-(2,6,7-trioxabicyclo[2.2.2]octan-4-ylmethoxy)-2,2-bis(2,6,7-trioxabicyclo[2.2.2]octan-4-ylmethoxymethyl)propoxy]methyl]propoxy]methyl]-2-(2,6,7-trioxabicyclo[2.2.2]octan-4-ylmethoxymethyl)propoxy]methyl]-2,6,7-trioxabicyclo[2.2.2]octane 在 盐酸 作用下， 以 甲醇 为溶剂， 反应 3.0h， 生成 2-[[3-[3-Hydroxy-2,2-bis(hydroxymethyl)propoxy]-2-[[3-[3-[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]-2,2-bis[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]-2,2-bis[[3-[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]-2,2-bis[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]methyl]propoxy]methyl]-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol
  参考文献：
  名称：

  Starburst polyether dendrimers

  摘要：

  DOI：

  10.1021/jo00233a002

文献信息

• Hollow Fiber Membrane and Preparing Method Thereof
  申请人：Bae Sung Su

  公开号：US20080261017A1

  公开（公告）日：2008-10-23

  The present invention relates to a polyvinylidene difluoride hollow fiber membrane and a method of preparing the same, and more particularly, to an improved polyvinylidene difluoride hollow fiber membrane and a preparation method thereof, in which a spinning solution consisting of polyvinylidene fluoride, alcohol dendrimer and organic solvent is prepared, and then is subjected to solidification by a wet-phase transition process, cleaning and drying, in which alcohol dendrimer that is an organic material as a pore former is introduced, allowing uniform disperse of alcohol dendrimer in polyvinylidene difluoride to form pores, with each having a high dispersion ability and a uniform size, and in which an excellent adhesion durability is imparted, owing to the use of a single material of polyvinylidene difluoride, unlike the conventional hollow fiber membrane preparation method in which pores are formed using existing inorganic particles.