N-{4-[(2R,3S,4S,5R,6R)-3,5-Dihydroxy-4-((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-6-((2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxymethyl)-tetrahydro-pyran-2-yloxy]-phenyl}-acrylamide | 442543-02-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: N-{4-[(2R,3S,4S,5R,6R)-3,5-Dihydroxy-4-((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-6-((2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxymethyl)-tetrahydro-pyran-2-yloxy]-phenyl}-acrylamide
• 英文别名: N-[4-[(2R,3S,4S,5R,6R)-3,5-dihydroxy-4-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enamide
• CAS: 442543-02-4
• 化学式: C₂₇H₃₉NO₁₇
• 分子量: 649.603
• InChiKey: GWLXOGFPRJUYKL-WIIYPHDNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -4.2
• 重原子数：
  45
• 可旋转键数：
  11
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  287
• 氢给体数：
  11
• 氢受体数：
  17

反应信息

• 作为产物：
  描述：

  对硝基苯-Alpha-D-吡喃甘露糖苷 在 palladium dihydroxide 三氟甲磺酸三甲基硅酯 、 氢气 作用下， 以 乙腈 为溶剂， 生成 N-{4-[(2R,3S,4S,5R,6R)-3,5-Dihydroxy-4-((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-6-((2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxymethyl)-tetrahydro-pyran-2-yloxy]-phenyl}-acrylamide
  参考文献：
  名称：

  Communication: A Facile Synthesis of a Glycoconjugate Cationic Polymer Carrying the 3,6-Branched α-D-Mannosyl Trisaccharide Cluster

  摘要：

  DOI：

  10.1080/07328300008544089

文献信息

• Communication: A Facile Synthesis of a Glycoconjugate Cationic Polymer Carrying the 3,6-Branched α-D-Mannosyl Trisaccharide Cluster
  作者：Hidehiko Tanaka、Yoshihiro Nishida、Kazukiyo Kobayashi

  DOI：10.1080/07328300008544089

  日期：2000.1