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Gal(b1-4)2-deoxy-b-D-araHex | 58634-82-5

中文名称
——
中文别名
——
英文名称
Gal(b1-4)2-deoxy-b-D-araHex
英文别名
(2S,3R,4S,5R,6R)-2-[(2R,3S,4R,6R)-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
Gal(b1-4)2-deoxy-b-D-araHex化学式
CAS
58634-82-5
化学式
C12H22O10
mdl
——
分子量
326.301
InChiKey
FDCIWBIYHZDLEG-PUGXJXRHSA-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):
    -3.8
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    169
  • 氢给体数:
    7
  • 氢受体数:
    10

反应信息

  • 作为产物:
    描述:
    1,3,6-tri-O-ethanoyl-4-O-(2,3,4,6-tetra-O-ethanoyl-β-D-galactosyl)-2-deoxy-β-D-glucose 在 sodium methylate 作用下, 以 甲醇 为溶剂, 反应 6.0h, 生成 (2S,3R,4S,5R,6R)-2-(((2R,3S,4R,6S)-4,6-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 、 Gal(b1-4)2-deoxy-b-D-araHex
    参考文献:
    名称:
    Synthesis of 2-deoxy-d-arabino/lyxo-hexopyranosyl disaccharides
    摘要:
    Synthesis of 2-deoxy-D-arabino/lyxo-hexopyranosyl disaccharides is reported. In these, the disaccharides contain 2-deoxy-arabino-hexopyranosyl and 2-deoxy-lyxo-hexopyranosyl sugars as either the reducing or the non-reducing or both the sugar units of the disaccharides. The activated 2-deoxy-1-thioglycosides served as the common precursors to prepare the 2-deoxy disaccharides with the above configurations. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2007.11.017
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文献信息

  • Synthesis of 2-deoxy-d-arabino/lyxo-hexopyranosyl disaccharides
    作者:Somak Paul、Narayanaswamy Jayaraman
    DOI:10.1016/j.carres.2007.11.017
    日期:2008.2
    Synthesis of 2-deoxy-D-arabino/lyxo-hexopyranosyl disaccharides is reported. In these, the disaccharides contain 2-deoxy-arabino-hexopyranosyl and 2-deoxy-lyxo-hexopyranosyl sugars as either the reducing or the non-reducing or both the sugar units of the disaccharides. The activated 2-deoxy-1-thioglycosides served as the common precursors to prepare the 2-deoxy disaccharides with the above configurations. (c) 2007 Elsevier Ltd. All rights reserved.
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