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7-dimethylallyloxy-5-hydroxy-3-methylchromone | 1131007-64-1

中文名称
——
中文别名
——
英文名称
7-dimethylallyloxy-5-hydroxy-3-methylchromone
英文别名
5-Hydroxy-3-methyl-7-(3-methylbut-2-enoxy)chromen-4-one
7-dimethylallyloxy-5-hydroxy-3-methylchromone化学式
CAS
1131007-64-1
化学式
C15H16O4
mdl
——
分子量
260.29
InChiKey
QUFCGVITIIOBDJ-UHFFFAOYSA-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):
    3.6
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    55.8
  • 氢给体数:
    1
  • 氢受体数:
    4

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:
    5,7-Dihydroxy-3-methylchromone1-溴-3-甲基-2-丁烯potassium carbonate 作用下, 以 丙酮 为溶剂, 反应 2.0h, 以65%的产率得到7-dimethylallyloxy-5-hydroxy-3-methylchromone
    参考文献:
    名称:
    Chromone and chromanone glucosides from Hypericum sikokumontanum and their anti-Helicobacter pylori activities
    摘要:
    Chromone glucosides, takanechromones A-C (1, 2 and S) and chromanone glucosides, named takanechromanones A and B (3 and 4), were isolated from the methanolic extracts of Hypericum sikokumontanum together with 27 known compounds. Their structures were established based on spectroscopic evidence. The isolated compounds and some chromone derivatives were assayed for antimicrobial activity against Helicobacter pylori and cytotoxicity against human cancer cell lines. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.phytochem.2008.11.006
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文献信息

  • Chromone and chromanone glucosides from Hypericum sikokumontanum and their anti-Helicobacter pylori activities
    作者:Naonobu Tanaka、Yoshiki Kashiwada、Tatsuro Nakano、Hirofumi Shibata、Tomihiko Higuchi、Michiko Sekiya、Yasumasa Ikeshiro、Yoshihisa Takaishi
    DOI:10.1016/j.phytochem.2008.11.006
    日期:2009.1
    Chromone glucosides, takanechromones A-C (1, 2 and S) and chromanone glucosides, named takanechromanones A and B (3 and 4), were isolated from the methanolic extracts of Hypericum sikokumontanum together with 27 known compounds. Their structures were established based on spectroscopic evidence. The isolated compounds and some chromone derivatives were assayed for antimicrobial activity against Helicobacter pylori and cytotoxicity against human cancer cell lines. (C) 2008 Elsevier Ltd. All rights reserved.
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