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ethyl 3-O-acetyl-4-azido-2,4,6-trideoxy-2-tetrachlorophthalimido-1-thio-β-D-galactopyranoside | 280569-38-2

中文名称
——
中文别名
——
英文名称
ethyl 3-O-acetyl-4-azido-2,4,6-trideoxy-2-tetrachlorophthalimido-1-thio-β-D-galactopyranoside
英文别名
[(2S,3R,4R,5S,6R)-5-azido-2-ethylsulfanyl-6-methyl-3-(4,5,6,7-tetrachloro-1,3-dioxoisoindol-2-yl)oxan-4-yl] acetate
ethyl 3-O-acetyl-4-azido-2,4,6-trideoxy-2-tetrachlorophthalimido-1-thio-β-D-galactopyranoside化学式
CAS
280569-38-2
化学式
C18H16Cl4N4O5S
mdl
——
分子量
542.227
InChiKey
HPFGNMYXBJTKRZ-JVJYRCIPSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    5.6
  • 重原子数:
    32
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    113
  • 氢给体数:
    0
  • 氢受体数:
    8

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    ethyl 3-O-acetyl-4-azido-2,4,6-trideoxy-2-tetrachlorophthalimido-1-thio-β-D-galactopyranosidemethyl 3-O-benzyl-6-O-chloroacetyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranosideN-碘代丁二酰亚胺三氟甲磺酸 、 4 A molecular sieve 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 0.33h, 以53%的产率得到methyl (3-O-acetyl-4-azido-2,4,6-trideoxy-2-tetrachlorophthalimido-β-D-galactopyranosyl)-(1->4)-3-O-benzyl-6-O-chloroacetyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside
    参考文献:
    名称:
    Synthetic Studies Towards theO-Specific Polysaccharide ofShigella Sonnei
    摘要:
    Synthetic routes are described to zwitter-ionic disaccharides that are diastereoisomerically related to frame-shifted repeating units of the title polysaccharide that contains 2-acetamido-4-amino-2,4,6-trideoxy-D-galactose and 2-acetamido-2-deoxy-L-altruronic acid. The intermediates corresponding to the trideoxygalactose residue feature acylamino functions at C-2 and an azido group at C-4. Best results were obtained with N-phthaloyl- and N-trichloroacetyl-protected derivatives. The intermediates corresponding to the uronic acid residue were either a D-altruronic acid-derived acceptor or a D-altrose-derived donor in which C-6 was oxidized after disaccharide formation.
    DOI:
    10.1080/07328300008544079
  • 作为产物:
    参考文献:
    名称:
    Synthetic Studies Towards theO-Specific Polysaccharide ofShigella Sonnei
    摘要:
    Synthetic routes are described to zwitter-ionic disaccharides that are diastereoisomerically related to frame-shifted repeating units of the title polysaccharide that contains 2-acetamido-4-amino-2,4,6-trideoxy-D-galactose and 2-acetamido-2-deoxy-L-altruronic acid. The intermediates corresponding to the trideoxygalactose residue feature acylamino functions at C-2 and an azido group at C-4. Best results were obtained with N-phthaloyl- and N-trichloroacetyl-protected derivatives. The intermediates corresponding to the uronic acid residue were either a D-altruronic acid-derived acceptor or a D-altrose-derived donor in which C-6 was oxidized after disaccharide formation.
    DOI:
    10.1080/07328300008544079
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