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10-azidodecyl 3,4-O-isopropylidene-β-D-galactopyranoside | 574737-33-0

中文名称
——
中文别名
——
英文名称
10-azidodecyl 3,4-O-isopropylidene-β-D-galactopyranoside
英文别名
——
10-azidodecyl 3,4-O-isopropylidene-β-D-galactopyranoside化学式
CAS
574737-33-0
化学式
C19H35N3O6
mdl
——
分子量
401.503
InChiKey
TWMYOBRWSNROFZ-UYTYNIKBSA-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):
    3.03
  • 重原子数:
    28.0
  • 可旋转键数:
    13.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    126.14
  • 氢给体数:
    2.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    10-azidodecyl 3,4-O-isopropylidene-β-D-galactopyranoside 在 4 A molecular sieve 、 camphor-10-sulfonic acid 、 sodium hydride 、 二正丁基氧化锡 作用下, 以 甲醇乙醚N,N-二甲基甲酰胺甲苯 为溶剂, 反应 36.0h, 生成 10-azadodecyl O-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-galactopyranoside
    参考文献:
    名称:
    Synthesis of polyanionic glycopolymers for the facile assembly of glycosyl arrays
    摘要:
    Polyanionic glycopolymers were synthesized aiming at establishing a simple process for assembling glycosyl arrays. The synthetic glycopolymers carry the key carbohydrate epitopes of alpha-D-galactobioside (Gb(2)), beta-lactoside, and U-D-mannopyranoside, each of which serves as a ligand of bacterial toxins and adhesion proteins. The Gb(2) epitope, prepared from penta-O-acetyl-D-galactopyranose, was coupled with poly(ethylene-alt-maleic anhydride) in a polymer reaction to afford a Gb(2)-embedded glycopolymer having also carboxylate (COO-) polyanions at the side chain. The polyanionic glycopolymer was then applied to a preparation of sugar-coated gold electrodes, which involves an alternating layer-by-layer adsorption based on electrostatic interactions. The presence of the Gb(2)-Coat on the surface was evidenced by Fourier transform infrared reflection absorption spectroscopy. The Gb(2)-coated glyco-chip was stable in 10 mM HEPES buffer containing 150 mM NaCl aq. Other glycopolymers carrying the beta-lactoside and alpha-D-mannopyranoside epitopes were applied to the same assembling process. The derived glycosyl arrays will be useful for detecting Shiga toxins, other pathogenic toxins and viruses when applied as glyco-chips for surface plasmon resonance or quartz crystal microbalance technique. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2005.03.102
  • 作为产物:
    描述:
    10-bromodecyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 在 sodium azide 、 camphor-10-sulfonic acid 、 sodium methylate 作用下, 以 甲醇N,N-二甲基甲酰胺丙酮 为溶剂, 反应 9.5h, 生成 10-azidodecyl 3,4-O-isopropylidene-β-D-galactopyranoside
    参考文献:
    名称:
    Synthesis of polyanionic glycopolymers for the facile assembly of glycosyl arrays
    摘要:
    Polyanionic glycopolymers were synthesized aiming at establishing a simple process for assembling glycosyl arrays. The synthetic glycopolymers carry the key carbohydrate epitopes of alpha-D-galactobioside (Gb(2)), beta-lactoside, and U-D-mannopyranoside, each of which serves as a ligand of bacterial toxins and adhesion proteins. The Gb(2) epitope, prepared from penta-O-acetyl-D-galactopyranose, was coupled with poly(ethylene-alt-maleic anhydride) in a polymer reaction to afford a Gb(2)-embedded glycopolymer having also carboxylate (COO-) polyanions at the side chain. The polyanionic glycopolymer was then applied to a preparation of sugar-coated gold electrodes, which involves an alternating layer-by-layer adsorption based on electrostatic interactions. The presence of the Gb(2)-Coat on the surface was evidenced by Fourier transform infrared reflection absorption spectroscopy. The Gb(2)-coated glyco-chip was stable in 10 mM HEPES buffer containing 150 mM NaCl aq. Other glycopolymers carrying the beta-lactoside and alpha-D-mannopyranoside epitopes were applied to the same assembling process. The derived glycosyl arrays will be useful for detecting Shiga toxins, other pathogenic toxins and viruses when applied as glyco-chips for surface plasmon resonance or quartz crystal microbalance technique. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2005.03.102
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