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2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-(2-acetamido-4,6-di-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-D-glucopyranose | 118700-98-4

中文名称
——
中文别名
——
英文名称
2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-(2-acetamido-4,6-di-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-D-glucopyranose
英文别名
Gal2Ac3Ac4Ac6Ac(b1-4)GlcNAc3Ac6Ac(b1-3)Gal2Ac4Ac6Ac(b1-4)Glc2Ac3Ac6Ac;[(2R,3R,4S,5R)-3-[(2S,3R,4S,5S,6R)-4-[(2S,3R,4R,5S,6R)-3-acetamido-4-acetyloxy-6-(acetyloxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-diacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-4,5-diacetyloxy-6-hydroxyoxan-2-yl]methyl acetate
2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-(2-acetamido-4,6-di-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-D-glucopyranose化学式
CAS
118700-98-4
化学式
C50H69NO33
mdl
——
分子量
1212.08
InChiKey
QFNWHFJVJGPGCC-UKTNOOTLSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

反应信息

  • 作为反应物:
    描述:
    2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-(2-acetamido-4,6-di-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-D-glucopyranose三氯乙腈 在 sodium hydride 作用下, 以 二氯甲烷 为溶剂, 反应 4.0h, 以74%的产率得到O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-(2-acetamido-4,6-di-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl trichloroacetimidate
    参考文献:
    名称:
    Bommer, Rene; Schmidt, Richard R., Liebigs Annalen der Chemie, 1989, p. 1107 - 1112
    摘要:
    DOI:
  • 作为产物:
    描述:
    acetyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-(2-acetamido-4,6-di-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-α,β-D-glucopyranoside 在 乙酸肼 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以83%的产率得到2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-(2-acetamido-4,6-di-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1->3)-(2,4,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-D-glucopyranose
    参考文献:
    名称:
    Bommer, Rene; Schmidt, Richard R., Liebigs Annalen der Chemie, 1989, p. 1107 - 1112
    摘要:
    DOI:
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