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Dodecyl β-D-ribofuranoside

中文名称
——
中文别名
——
英文名称
Dodecyl β-D-ribofuranoside
英文别名
(2R,3R,4S,5R)-2-dodecoxy-5-(hydroxymethyl)oxolane-3,4-diol
Dodecyl β-D-ribofuranoside化学式
CAS
——
化学式
C17H34O5
mdl
——
分子量
318.454
InChiKey
NXWOMTNQJLXSFE-QBPKDAKJSA-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):
    4.1
  • 重原子数:
    22
  • 可旋转键数:
    13
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    79.2
  • 氢给体数:
    3
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    D-核糖十二烷醇 在 silica-alumina cracking catalyst HA-HPV 作用下, 70.0 ℃ 、2.0 kPa 条件下, 反应 24.0h, 生成 Dodecyl β-D-ribofuranoside
    参考文献:
    名称:
    Synthesis of Alkyl Fructosides Using Solid Acid Catalysts. Part I: Silica-Alumina Cracking Catalysts
    摘要:
    Silica-alumina cracking catalysts and acid clays efficiently catalyze the 2-O-alkylation of D-fructose with long chain alcohols. Under the conditions applied virtually no degradation of fructose is observed. L-Sorbose and the aldopentoses also undergo silica-alumina-catalyzed alkylation. The rate of conversion is related to the solubility of the monosaccharide and the stability of the intermediate oxocarbenium ion. Best results in fructose alkylation are obtained by applying a recirculation method with butyl fructoside as soluble intermediate.
    DOI:
    10.1080/07328309608005657
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文献信息

  • Synthesis of Alkyl Fructosides Using Solid Acid Catalysts. Part I: Silica-Alumina Cracking Catalysts
    作者:A. T.J.W. de Goede、M. P.J. van Deurzen、I. G. van der Leij、A. M. van der Heijden、J. M.A. Baas、F. van Rantwijk、H. van Bekkum
    DOI:10.1080/07328309608005657
    日期:1996.4
    Silica-alumina cracking catalysts and acid clays efficiently catalyze the 2-O-alkylation of D-fructose with long chain alcohols. Under the conditions applied virtually no degradation of fructose is observed. L-Sorbose and the aldopentoses also undergo silica-alumina-catalyzed alkylation. The rate of conversion is related to the solubility of the monosaccharide and the stability of the intermediate oxocarbenium ion. Best results in fructose alkylation are obtained by applying a recirculation method with butyl fructoside as soluble intermediate.
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