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β-D-glucopyranosyl-(1→6)-arbutin | 7013-25-4

中文名称
——
中文别名
——
英文名称
β-D-glucopyranosyl-(1→6)-arbutin
英文别名
p-Hydroxyphenyl-β-gentiobiosid;Hydrochinon-β-gentiobiosid;Glc(b1-6)Glc(b)-O-Ph(4-OH);(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methoxy]oxane-3,4,5-triol
β-D-glucopyranosyl-(1→6)-arbutin化学式
CAS
7013-25-4
化学式
C18H26O12
mdl
——
分子量
434.397
InChiKey
OGLZRXDYSXDVNG-NNUBVHJDSA-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):
    -2.9
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    199
  • 氢给体数:
    8
  • 氢受体数:
    12

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:
    Sucrose熊果苷 在 sodium citrate 、 α-glucosidase 作用下, 以 phosphate buffer 为溶剂, 反应 20.0h, 以50%的产率得到β-D-glucopyranosyl-(1→6)-arbutin
    参考文献:
    名称:
    A simple and efficient one-step, regioselective, enzymatic glucosylation of arbutin by α-glucosidase
    摘要:
    4-Hydroxyphenyl-beta-isomaltoside has been synthesized by alpha-glucosidase assisted transglycosylation between arbutin as acceptor and sucrose as donor molecules, respectively. Optimum conditions for the transglucosylation reaction were 40 degrees C for 20 h with 10 mM arbutin and 1.5 M sucrose in a 100 mM sodium citrate/phosphate buffer at pH 5.0. The new glucoside was obtained in a 50% molar yield with respect to arbutin. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.07.152
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文献信息

  • A simple and efficient one-step, regioselective, enzymatic glucosylation of arbutin by α-glucosidase
    作者:Nenad B. Milosavić、Radivoje M. Prodanović、Ratko M. Jankov
    DOI:10.1016/j.tetlet.2007.07.152
    日期:2007.10
    4-Hydroxyphenyl-beta-isomaltoside has been synthesized by alpha-glucosidase assisted transglycosylation between arbutin as acceptor and sucrose as donor molecules, respectively. Optimum conditions for the transglucosylation reaction were 40 degrees C for 20 h with 10 mM arbutin and 1.5 M sucrose in a 100 mM sodium citrate/phosphate buffer at pH 5.0. The new glucoside was obtained in a 50% molar yield with respect to arbutin. (C) 2007 Elsevier Ltd. All rights reserved.
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