(2R,4R)-2-undecyl-4-thiazolidinecarboxylic acid

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (2R,4R)-2-undecyl-4-thiazolidinecarboxylic acid
• 英文别名: (2R,4R)-2-undecyl-1,3-thiazolidine-4-carboxylic acid
• 化学式: C₁₅H₂₉NO₂S
• 分子量: 287.467
• InChiKey: FNBSOIBCKUUVJJ-UONOGXRCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  19
• 可旋转键数：
  11
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.93
• 拓扑面积：
  74.6
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  乙酸酐 、 (2R,4R)-2-undecyl-4-thiazolidinecarboxylic acid 在 base 作用下， 以 水 为溶剂， 生成 (2R,4R)-3-Acetyl-2-undecyl-thiazolidine-4-carboxylic acid
  参考文献：
  名称：

  Chiral discrimination in capillary electrophoresis using novel anionic surfactants related to cysteine

  摘要：

  Two novel cysteine-based, anionic, chiral surfactants have been designed and prepared from readily available starting materials; these molecules were successfully used as chiral selectors in micellar electrokinetic capillary chromatography (MECC).

  DOI：

  10.1039/c39950001575
• 作为产物：
  描述：

  十二醛 、 L-半胱氨酸盐酸盐无水物 生成 (2R,4R)-2-undecyl-4-thiazolidinecarboxylic acid
  参考文献：
  名称：

  Chiral discrimination in capillary electrophoresis using novel anionic surfactants related to cysteine

  摘要：

  Two novel cysteine-based, anionic, chiral surfactants have been designed and prepared from readily available starting materials; these molecules were successfully used as chiral selectors in micellar electrokinetic capillary chromatography (MECC).

  DOI：

  10.1039/c39950001575

文献信息

• Chiral discrimination in capillary electrophoresis using novel anionic surfactants related to cysteine
  作者：Vern de Biasi、John Senior、Janusz A. Zukowski、R. Curtis Haltiwanger、Drake S. Eggleston、Patrick Camilleri

  DOI：10.1039/c39950001575

  日期：——

  Two novel cysteine-based, anionic, chiral surfactants have been designed and prepared from readily available starting materials; these molecules were successfully used as chiral selectors in micellar electrokinetic capillary chromatography (MECC).