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(3R,5R,6S,7E,9S)-megastigman-7-en-5,6-epoxy-3,9-diol 3-O-β-D-glucopyranoside | 1033434-15-9

中文名称
——
中文别名
——
英文名称
(3R,5R,6S,7E,9S)-megastigman-7-en-5,6-epoxy-3,9-diol 3-O-β-D-glucopyranoside
英文别名
euodionoside B;(3S,5R,6S,7E,9R)-3-hydroxy-5,6-epoxy-β-ionyl-3-O-β-D-glucopyranoside;(2R,3R,4S,5S,6R)-2-[[(1R,3R,6S)-6-[(E,3S)-3-hydroxybut-1-enyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
(3R,5R,6S,7E,9S)-megastigman-7-en-5,6-epoxy-3,9-diol 3-O-β-D-glucopyranoside化学式
CAS
1033434-15-9
化学式
C19H32O8
mdl
——
分子量
388.458
InChiKey
SMBCGBWABYMHIN-GORYWLCDSA-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):
    -0.5
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    132
  • 氢给体数:
    5
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    (3R,5R,6S,7E,9S)-megastigman-7-en-5,6-epoxy-3,9-diol 3-O-β-D-glucopyranoside 作用下, 以91%的产率得到(1R,3R,6S)-6-[(E,3S)-3-hydroxybut-1-enyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol
    参考文献:
    名称:
    Euodionosides A–G: Megastigmane glucosides from leaves of Euodia meliaefolia
    摘要:
    From a 1-BuOH-soluble fraction of the MeOH extract of leaves of Euodia metiaefolia, collected in Okinawa, seven megastigmane glucosides, named euodionosides A-G, were isolated together with three known megastgmane glucosides, and two aliphatic and three phenolic compounds. Their structures were elucidated through a combination of spectroscopic analyses and application of the modified Mosher's method. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.phytochem.2008.01.020
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