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Acetic acid (3aR,5R,6R,6aS)-5-acetoxymethyl-2-icosyloxy-2-oxo-hexahydro-2λ5-furo[2,3-d][1,2]oxaphosphol-6-yl ester | 543691-28-7

中文名称
——
中文别名
——
英文名称
Acetic acid (3aR,5R,6R,6aS)-5-acetoxymethyl-2-icosyloxy-2-oxo-hexahydro-2λ5-furo[2,3-d][1,2]oxaphosphol-6-yl ester
英文别名
[(3aR,5R,6R,6aS)-6-acetyloxy-2-icosoxy-2-oxido-3a,5,6,6a-tetrahydro-3H-furo[2,3-d]oxaphosphol-2-ium-5-yl]methyl acetate
Acetic acid (3aR,5R,6R,6aS)-5-acetoxymethyl-2-icosyloxy-2-oxo-hexahydro-2λ<sup>5</sup>-furo[2,3-d][1,2]oxaphosphol-6-yl ester化学式
CAS
543691-28-7
化学式
C30H55O8P
mdl
——
分子量
574.736
InChiKey
GLTHWNULZDPSCP-YJFDKHHDSA-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):
    8.8
  • 重原子数:
    39
  • 可旋转键数:
    25
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    103
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    Acetic acid (3aR,5R,6R,6aS)-5-acetoxymethyl-2-icosyloxy-2-oxo-hexahydro-2λ5-furo[2,3-d][1,2]oxaphosphol-6-yl estersodium hydroxide 、 Dowex 50W (H(+) form) 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以85%的产率得到((2R,3S,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-ylmethyl)-phosphonic acid monoicosyl ester
    参考文献:
    名称:
    Synthesis of sugar-derived phostones by activation of γ-hydroxyphosphonic acids
    摘要:
    Treatment of carbohydrate-derived gamma-hydroxyphosphonic acids under usual acetylation conditions affords the corresponding phostones in good yield. The method could be used for the preparation of free phostones as well as alpha- and beta-phosphonomethylarabinose. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(03)00240-5
  • 作为产物:
    描述:
    乙酸酐 、 在 三乙胺 作用下, 以 吡啶 为溶剂, 反应 15.0h, 以51%的产率得到Acetic acid (2S,3S,4R,5R)-4-acetoxy-5-acetoxymethyl-2-(hydroxy-icosyloxy-phosphorylmethyl)-tetrahydro-furan-3-yl ester
    参考文献:
    名称:
    Synthesis of sugar-derived phostones by activation of γ-hydroxyphosphonic acids
    摘要:
    Treatment of carbohydrate-derived gamma-hydroxyphosphonic acids under usual acetylation conditions affords the corresponding phostones in good yield. The method could be used for the preparation of free phostones as well as alpha- and beta-phosphonomethylarabinose. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(03)00240-5
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