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(2R,4R,5R,6R)-6-((R)-1,2-Dimethoxy-ethyl)-4,5-dimethoxy-2-((2R,3R,4R,5R,7R)-2,3,4,5,7-pentamethoxy-7-methoxycarbonyl-heptyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester | 121275-90-9

中文名称
——
中文别名
——
英文名称
(2R,4R,5R,6R)-6-((R)-1,2-Dimethoxy-ethyl)-4,5-dimethoxy-2-((2R,3R,4R,5R,7R)-2,3,4,5,7-pentamethoxy-7-methoxycarbonyl-heptyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester
英文别名
——
(2R,4R,5R,6R)-6-((R)-1,2-Dimethoxy-ethyl)-4,5-dimethoxy-2-((2R,3R,4R,5R,7R)-2,3,4,5,7-pentamethoxy-7-methoxycarbonyl-heptyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester化学式
CAS
121275-90-9
化学式
C27H50O15
mdl
——
分子量
614.685
InChiKey
KXTCJNQTXKCDEE-DDIXEZJCSA-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

反应信息

  • 作为反应物:
    描述:
    (2R,4R,5R,6R)-6-((R)-1,2-Dimethoxy-ethyl)-4,5-dimethoxy-2-((2R,3R,4R,5R,7R)-2,3,4,5,7-pentamethoxy-7-methoxycarbonyl-heptyloxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 生成 (2R,4R,5R,6R,7R)-8-[(2R,4R,5R,6R)-6-((R)-1,2-Dimethoxy-ethyl)-2-hydroxymethyl-4,5-dimethoxy-tetrahydro-pyran-2-yloxy]-2,4,5,6,7-pentamethoxy-octan-1-ol
    参考文献:
    名称:
    GLC-MS of reduced, acetylated, and methylated (2 → 4)- and (2 → 8)-linked disaccharides of 3-deoxy-pD-manno-octulopyranosonic acid (Kdo)
    摘要:
    Synthetic alpha- and beta-(2 --> 4)- and alpha- and beta-(2 --> 8)-linked disaccharides of 3-deoxy-D-manno-octulopyranosonic acid (Kdo), of which the synthesis of the beta-(2 --> 4)-linked compound is described here, were used to develop a simple GLC-MS method for the determination of their anomeric configuration. The GLC and GLC-MS data for the reduced and acetylated or methylated derivatives of the above compounds indicate the a-linked synthetic disaccharides to be identical to those.isolated from bacterial lipopolysaccharides.
    DOI:
    10.1016/0008-6215(92)84008-g
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