2,2,2-trifluoro-N-((2-(2-(2-methoxyethoxy)ethoxy)-1,3-dioxolan-4-yl)methyl)acetamide | 1227059-95-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2,2,2-trifluoro-N-((2-(2-(2-methoxyethoxy)ethoxy)-1,3-dioxolan-4-yl)methyl)acetamide
• CAS: 1227059-95-1
• 化学式: C₁₁H₁₈F₃NO₆
• 分子量: 317.262
• InChiKey: CJMVUIZRLNYJTB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.04
• 重原子数：
  21.0
• 可旋转键数：
  9.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  75.25
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  2,2,2-trifluoro-N-((2-(2-(2-methoxyethoxy)ethoxy)-1,3-dioxolan-4-yl)methyl)acetamide 在 sodium hydroxide 作用下， 以 四氢呋喃 、 水 为溶剂， 生成
  参考文献：
  名称：

  Tuning the pH sensitivities of orthoester based compounds for drug delivery applications by simple chemical modification

  摘要：

  Orthoesters are acid-sensitive moieties that allow substantial structural diversity for biological applications including drug delivery. Here, the pH-sensitivity of a range of novel orthoester based compounds was compared in the range 7.5-4.5 that is characteristic of the increased acidification during endocytosis. We find that simple modifications close to the orthoester had major effects on both the rate and extent of hydrolysis, suggesting this could be exploited for activating drug delivery systems on endocytic pathways. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.02.035
• 作为产物：
  描述：

  2,2,2-trifluoro-N-(2-methoxy-[1,3]-dioxolan-4-ylmethyl)acetamide 、 二乙二醇单甲醚 在 4-甲基苯磺酸吡啶 作用下， 以 甲苯 为溶剂， 生成 2,2,2-trifluoro-N-((2-(2-(2-methoxyethoxy)ethoxy)-1,3-dioxolan-4-yl)methyl)acetamide
  参考文献：
  名称：

  Tuning the pH sensitivities of orthoester based compounds for drug delivery applications by simple chemical modification

  摘要：

  Orthoesters are acid-sensitive moieties that allow substantial structural diversity for biological applications including drug delivery. Here, the pH-sensitivity of a range of novel orthoester based compounds was compared in the range 7.5-4.5 that is characteristic of the increased acidification during endocytosis. We find that simple modifications close to the orthoester had major effects on both the rate and extent of hydrolysis, suggesting this could be exploited for activating drug delivery systems on endocytic pathways. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.02.035