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| 1119276-02-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1119276-02-6
化学式
C43H48O9
mdl
——
分子量
708.849
InChiKey
HWHOIBCIRHSEQP-ZBIQRMRKSA-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):
    7.13
  • 重原子数:
    52.0
  • 可旋转键数:
    15.0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    83.07
  • 氢给体数:
    0.0
  • 氢受体数:
    9.0

反应信息

  • 作为反应物:
    描述:
    乙硫醇 在 ammonium cerium (IV) nitrate 作用下, 以 乙腈 为溶剂, 反应 16.25h, 以40%的产率得到ethyl 3,6-di-O-benzyl-4-O-(2,3-di-O-benzyl-α-D-glucopyranosyl)-2-deoxy-1-thio-β-D-arabino-hexopyranoside
    参考文献:
    名称:
    Synthesis of 2-deoxy cyclic and linear oligosaccharides by oligomerization of monomers
    摘要:
    Cyclic and linear oligosaccharides constituted with 2-deoxy sugar units are synthesized by an oligomerization reaction involving activated thioglycoside monomers, consisting of a 2-deoxy sugar unit. The oligomerization promoter plays an important role in the formation of either the cyclic- or the linear oligosaccharides. Encapsulation abilities of a 2-deoxy cyclic hexamer with p-nitrophenot, by a H-1 NMR method, showed complexation of the guest molecule with the host molecule. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2008.10.026
  • 作为产物:
    描述:
    溴甲苯 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 、 mineral oil 为溶剂, 反应 4.0h, 以75%的产率得到
    参考文献:
    名称:
    Synthesis of 2-deoxy cyclic and linear oligosaccharides by oligomerization of monomers
    摘要:
    Cyclic and linear oligosaccharides constituted with 2-deoxy sugar units are synthesized by an oligomerization reaction involving activated thioglycoside monomers, consisting of a 2-deoxy sugar unit. The oligomerization promoter plays an important role in the formation of either the cyclic- or the linear oligosaccharides. Encapsulation abilities of a 2-deoxy cyclic hexamer with p-nitrophenot, by a H-1 NMR method, showed complexation of the guest molecule with the host molecule. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2008.10.026
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