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D-<2-13C>xylose | 131771-69-2

中文名称
——
中文别名
——
英文名称
D-<2-13C>xylose
英文别名
Xylose-2-13C;(2R,3S,4R)-2,3,4,5-tetrahydroxy(213C)pentanal
D-<2-13C>xylose化学式
CAS
131771-69-2
化学式
C5H10O5
mdl
——
分子量
151.12
InChiKey
PYMYPHUHKUWMLA-AXXUHBFTSA-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):
    -2.3
  • 重原子数:
    10
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    98
  • 氢给体数:
    4
  • 氢受体数:
    5

SDS

SDS:f6070d76c9f6694a7b3b124c8a5cc538
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    D-核糖-1-13C624>-->resin 作用下, 以 为溶剂, 反应 6.5h, 以0.16%的产率得到D-<2-13C>xylose
    参考文献:
    名称:
    Paramolybdate anion-exchange resin, an improved catalyst for the C-1–C-2 rearrangement and 2-epimerization of aldoses
    摘要:
    Aqueous solutions of molybdate at 90 degrees bring about the inversion of the C-1-C-2 fragment of aldoses having four or more carbon atoms, generating thermodynamically equilibrated mixtures of the starting aldose and its 2-epimer. In some cases, notably with the aldopentoses, substantial proportions of the 3-epimers are produced, as well as 2-epimers that have not undergone inversion of the C-1-C-2 fragment. These side-reactions can be controlled by using the paramolybdate form of an anion-exchange resin (AG MP-1) together with the formate form of the same resin. The latter acts to scavenge unbound molybdate and paramolybdate anions that appear to be responsible for the side reactions.
    DOI:
    10.1016/s0008-6215(00)90268-4
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文献信息

  • Paramolybdate anion-exchange resin, an improved catalyst for the C-1–C-2 rearrangement and 2-epimerization of aldoses
    作者:Edward L. Clark、Michael L. Hayes、Robert Barker
    DOI:10.1016/s0008-6215(00)90268-4
    日期:1986.10
    Aqueous solutions of molybdate at 90 degrees bring about the inversion of the C-1-C-2 fragment of aldoses having four or more carbon atoms, generating thermodynamically equilibrated mixtures of the starting aldose and its 2-epimer. In some cases, notably with the aldopentoses, substantial proportions of the 3-epimers are produced, as well as 2-epimers that have not undergone inversion of the C-1-C-2 fragment. These side-reactions can be controlled by using the paramolybdate form of an anion-exchange resin (AG MP-1) together with the formate form of the same resin. The latter acts to scavenge unbound molybdate and paramolybdate anions that appear to be responsible for the side reactions.
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