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6-O-(α-L-rhamnopyranosyl)-D-galactopyranose | 552-74-9

中文名称
——
中文别名
——
英文名称
6-O-(α-L-rhamnopyranosyl)-D-galactopyranose
英文别名
O-α-L-rhamnopyranosyl-(1-6)-D-galactose;6-O-α-L-rhamnopyranosyl-D-galactose;Robinobiose;6-O-(6-Deoxy-I+/--L-mannopyranosyl)-D-galactopyranose;(3R,4S,5R,6R)-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxane-2,3,4,5-tetrol
6-O-(α-L-rhamnopyranosyl)-D-galactopyranose化学式
CAS
552-74-9
化学式
C12H22O10
mdl
——
分子量
326.301
InChiKey
OVVGHDNPYGTYIT-PDYCYQMRSA-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

物化性质

  • 沸点:
    598.0±50.0 °C(Predicted)
  • 密度:
    1.66±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -4.2
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 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

  • 作为反应物:
    描述:
    6-O-(α-L-rhamnopyranosyl)-D-galactopyranoseAPTS 在 sodium cyanoborohydride 、 溶剂黄146 作用下, 以 四氢呋喃 为溶剂, 反应 20.0h, 生成
    参考文献:
    名称:
    Synthesis of fluorescently labelled rhamnosides: probes for the evaluation of rhamnogalacturonan II biosynthetic enzymes
    摘要:
    Three fluorescently labelled saccharides 10-12, representing structures found in pectic glycan rhamnogalacturonan II (RG-II), were synthesised by chemical glycosylation of O-6 of diacetone-D-galactose followed by deprotection and reductive amination with amino-substituted fluorophore APTS. This convenient method installs a common aminogalactitol-based tether in order to preserve the integrity of the reducing end of specific carbohydrates of interest. APTS-labelled glycans prepared in this manner were purified by carbohydrate gel electrophoresis and subjected to capillary electrophoresis analysis, as a basis for the subsequent development of high sensitivity assays for RG-II-active enzymes. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.03.039
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