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cholesterol-3β-yl 2,3,4-tri-O-benzoyl-6-S-phenyl-6-thio-β-D-galactopyranoside | 402730-89-6

中文名称
——
中文别名
——
英文名称
cholesterol-3β-yl 2,3,4-tri-O-benzoyl-6-S-phenyl-6-thio-β-D-galactopyranoside
英文别名
[(2S,3R,4S,5R,6R)-4,5-dibenzoyloxy-6-[[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-2-(phenylsulfanylmethyl)oxan-3-yl] benzoate
cholesterol-3β-yl 2,3,4-tri-O-benzoyl-6-S-phenyl-6-thio-β-D-galactopyranoside化学式
CAS
402730-89-6
化学式
C60H72O8S
mdl
——
分子量
953.293
InChiKey
VKFQKUHQFIANPQ-YWXKXGACSA-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):
    16
  • 重原子数:
    69
  • 可旋转键数:
    19
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    123
  • 氢给体数:
    0
  • 氢受体数:
    9

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

  • 作为反应物:
    描述:
    甲醇cholesterol-3β-yl 2,3,4-tri-O-benzoyl-6-S-phenyl-6-thio-β-D-galactopyranoside吡啶磺酰氯 、 mercury dichloride 作用下, 以 四氯化碳二氯甲烷 为溶剂, 以65%的产率得到methyl (cholesterol-3β-yl 2,3,4-tri-O-benzoyl-β-D-galactopyranoside)uronate
    参考文献:
    名称:
    6-S-Phenyl-glycopyranosides as ready precursors to the synthesis of glycuronides
    摘要:
    6-S-Phenyl-gluco/galactopyranosides, readily prepared from the corresponding 6-hydroxy-glycosides, were demonstrated to be effective glycosyl donors or acceptors. The resulting coupling products were then easily converted into the corresponding glycuronidecontaining compounds under mild conditions. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00959-0
  • 作为产物:
    描述:
    1,2,3,4-tetra-O-benzoyl-6-S-phenyl-6-thio-β-D-galactopyranoside 在 三氟甲磺酸三甲基硅酯1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 四氢呋喃甲醇二氯甲烷 为溶剂, 反应 0.5h, 生成 cholesterol-3β-yl 2,3,4-tri-O-benzoyl-6-S-phenyl-6-thio-β-D-galactopyranoside
    参考文献:
    名称:
    6-S-Phenyl-glycopyranosides as ready precursors to the synthesis of glycuronides
    摘要:
    6-S-Phenyl-gluco/galactopyranosides, readily prepared from the corresponding 6-hydroxy-glycosides, were demonstrated to be effective glycosyl donors or acceptors. The resulting coupling products were then easily converted into the corresponding glycuronidecontaining compounds under mild conditions. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00959-0
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文献信息

  • 6-S-Phenyl-glycopyranosides as ready precursors to the synthesis of glycuronides
    作者:Biao Yu、Xiangming Zhu、Yongzheng Hui
    DOI:10.1016/s0040-4020(01)00959-0
    日期:2001.11
    6-S-Phenyl-gluco/galactopyranosides, readily prepared from the corresponding 6-hydroxy-glycosides, were demonstrated to be effective glycosyl donors or acceptors. The resulting coupling products were then easily converted into the corresponding glycuronidecontaining compounds under mild conditions. (C) 2001 Elsevier Science Ltd. All rights reserved.
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