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4-methoxyphenyl (α-D-galactofuranosyl)-(1->3)-(α-L-rhamnopyranosyl)-(1->2)-(α-L-rhamnopyranosyl)-(1->3)-(α-D-galactopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside | 1203549-88-5

中文名称
——
中文别名
——
英文名称
4-methoxyphenyl (α-D-galactofuranosyl)-(1->3)-(α-L-rhamnopyranosyl)-(1->2)-(α-L-rhamnopyranosyl)-(1->3)-(α-D-galactopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside
英文别名
Galf(a1-3)Rha(a1-2)Rha(a1-3)Gal(a1-3)Gal(b1-4)Glc(b)-O-Ph(4-OMe);(2S,3R,4R,5R,6S)-5-[(2S,3R,4R,5S,6S)-4-[(2R,3R,4R,5S)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-6-[(2R,3R,4S,5S,6R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-(4-methoxyphenoxy)oxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-methyloxane-3,4-diol
4-methoxyphenyl (α-D-galactofuranosyl)-(1->3)-(α-L-rhamnopyranosyl)-(1->2)-(α-L-rhamnopyranosyl)-(1->3)-(α-D-galactopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside化学式
CAS
1203549-88-5
化学式
C43H68O30
mdl
——
分子量
1064.99
InChiKey
HVTMPVUWXWVBMW-CDYKEWCLSA-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):
    -7.8
  • 重原子数:
    73
  • 可旋转键数:
    18
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    464
  • 氢给体数:
    17
  • 氢受体数:
    30

反应信息

  • 作为产物:
    描述:
    在 20% palladium(II) hydroxide on carbon 、 氢气 作用下, 以 甲醇 为溶剂, 反应 24.0h, 以340 mg的产率得到4-methoxyphenyl (α-D-galactofuranosyl)-(1->3)-(α-L-rhamnopyranosyl)-(1->2)-(α-L-rhamnopyranosyl)-(1->3)-(α-D-galactopyranosyl)-(1->3)-(β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside
    参考文献:
    名称:
    Concise Synthesis of a Hexasaccharide Related to the Adhesin Receptor of Streptococcus oralis ATCC 55229
    摘要:
    A concise synthesis of a hexasaccharide related to the adhesin receptor of Streptococcus oralis ATCC 55229 (previously characterized as Streptococcus sanguis H1) has been achieved in excellent yield. A general glycosylation condition has been used throughout the synthetic scheme. All glycosylation steps and protecting group functionalization steps are high yielding and suitable for scale-up preparation.
    DOI:
    10.1080/07328300903261554
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