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2,4,6-Tri-O-methyl-β-D-galactopyranose | 90865-30-8

中文名称
——
中文别名
——
英文名称
2,4,6-Tri-O-methyl-β-D-galactopyranose
英文别名
O2,O4,O6-trimethyl-D-galactose;O2,O4,O6-Trimethyl-D-galactopyranose;β-2.4.6-Tri-O-methyl-galactosid;2,4,6-Tri-O-methyl-D-galactopyranose;2,4,6-Tri-O-methyl-D-galactose;2,4,6-Tri-O-methyl-D-galaktose;(3R,4S,5R,6R)-3,5-dimethoxy-6-(methoxymethyl)oxane-2,4-diol
2,4,6-Tri-O-methyl-β-D-galactopyranose化学式
CAS
90865-30-8
化学式
C9H18O6
mdl
——
分子量
222.238
InChiKey
UTLUVTKMAWSZKV-MBOVONDJSA-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:
    360.900±42.00 °C(Press: 760.00 Torr)(predicted)
  • 密度:
    1.220±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.26
  • 重原子数:
    15.0
  • 可旋转键数:
    4.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    77.38
  • 氢给体数:
    2.0
  • 氢受体数:
    6.0

反应信息

  • 作为产物:
    描述:
    (2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-3,5-dihydroxy-2-[(2R,3R,4S,5R,6R)-5-hydroxy-4-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6S,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxan-4-yl]oxyoxane-3,4,5-triol 、 碘甲烷 生成 2,4,6-Tri-O-methyl-β-D-galactopyranose
    参考文献:
    名称:
    UNIYAI, G. C.;AGRAWAL, P. K.;THAKUR, R. S.;SATI, O. P., PHYTOCHEMISTRY, 29,(1990) N, C. 937-940
    摘要:
    DOI:
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文献信息

  • Formation of Homooligosaccharides Using Base-Promoted Glycosylation of Unprotected Glycosyl Fluorides
    作者:Andreas Steinmann、Julian Thimm、Martin Matwiejuk、Joachim Thiem
    DOI:10.1021/ma100191d
    日期:2010.4.27
    Homooligomeric saccharides are of general interest with potential applications in chemical, pharmaceutical, and food industry as well as for materials with novel properties. This contribution describes a methodology of a base-promoted "single step self-oligomerization" of glycosyl fluorides as donors leading to oligomers with up to similar to 25 saccharide units. The influences of base and reaction time were examined. Linkage analysis of the corresponding alditol acetates by GC/MS allowed for calculation of average structural elements of oligomers.
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