6-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-2-methylquinoline | 874949-61-8

• 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: 6-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-2-methylquinoline
• 英文别名: [(2R,3R,4S,5R,6S)-3,4,5-tribenzoyloxy-6-(2-methylquinolin-6-yl)oxyoxan-2-yl]methyl benzoate
• CAS: 874949-61-8
• 化学式: C₄₄H₃₅NO₁₀
• 分子量: 737.763
• InChiKey: NZZRRTOJAVTMSG-GDJDUYBCSA-N

物化性质

• 沸点：
  850.6±65.0 °C(predicted)
• 密度：
  1.37±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  8.8
• 重原子数：
  55
• 可旋转键数：
  15
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.16
• 拓扑面积：
  137
• 氢给体数：
  0
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  6-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-2-methylquinoline 在 sodium methylate 作用下， 以 甲醇 为溶剂， 反应 12.0h， 以90%的产率得到6-(β-D-glucopyranosyl)-quinaldine
  参考文献：
  名称：

  Synthesis of New Cholesterol- and Sugar-Anchored Squaraine Dyes:  Further Evidence of How Electronic Factors Influence Dye Formation

  摘要：

  Synthesis of new quinaldine-based squaraine dyes linked to cellular recognition elements that exhibit near-infrared absorption (> 740 nm) are described. Both product analysis and theoretical calculations substantiate the interesting electronic effects of various substituents in the dye formation reaction. These results are useful in the synthesis of symmetrical and unsymmetrical squaraine dyes that can have potential biological and photodynamic therapeutical applications.

  DOI：

  10.1021/ol052639j
• 作为产物：
  描述：

  6-羟基-2-甲基喹啉 、 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl bromide 在 sodium hydroxide 、 四丁基溴化铵 作用下， 以 氯仿 为溶剂， 反应 3.0h， 以20%的产率得到6-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-2-methylquinoline
  参考文献：
  名称：

  Synthesis of New Cholesterol- and Sugar-Anchored Squaraine Dyes:  Further Evidence of How Electronic Factors Influence Dye Formation

  摘要：

  Synthesis of new quinaldine-based squaraine dyes linked to cellular recognition elements that exhibit near-infrared absorption (> 740 nm) are described. Both product analysis and theoretical calculations substantiate the interesting electronic effects of various substituents in the dye formation reaction. These results are useful in the synthesis of symmetrical and unsymmetrical squaraine dyes that can have potential biological and photodynamic therapeutical applications.

  DOI：

  10.1021/ol052639j