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3-(4-Hydroxyphenyl)-7-(oxan-2-yloxy)chromen-4-one | 935659-64-6

中文名称
——
中文别名
——
英文名称
3-(4-Hydroxyphenyl)-7-(oxan-2-yloxy)chromen-4-one
英文别名
——
3-(4-Hydroxyphenyl)-7-(oxan-2-yloxy)chromen-4-one化学式
CAS
935659-64-6
化学式
C20H18O5
mdl
——
分子量
338.36
InChiKey
RHAPLFOKTQVFDY-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):
    3.7
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    3-(4-Hydroxyphenyl)-7-(oxan-2-yloxy)chromen-4-onepotassium carbonate对甲苯磺酸 作用下, 以 四氢呋喃甲醇丙酮 为溶剂, 反应 6.0h, 生成 conrauinone D
    参考文献:
    名称:
    Practical and efficient entry to isoflavones by Pd(0)/C-mediated Suzuki–Miyaura reaction. Total synthesis of geranylated isoflavones
    摘要:
    A scalable synthesis of isoflavones taking advantage of the Suzuki-Miyaura reaction catalyzed by Pd(0)/C is described. The approach developed has been extended to the total synthesis of 7-O-geranylformononetin, griffonianone D, and conrauinone D, which did not display cytotoxicity against human HeLa carcinoma cells. In addition, this study established unambiguously the absolute configuration of natural griffonianone D. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.01.062
  • 作为产物:
    描述:
    2,4-二羟基苯乙酮 在 palladium on activated charcoal 吡啶4-甲基苯磺酸吡啶 、 sodium carbonate 作用下, 以 乙二醇二甲醚二氯甲烷氯仿 为溶剂, 反应 20.0h, 生成 3-(4-Hydroxyphenyl)-7-(oxan-2-yloxy)chromen-4-one
    参考文献:
    名称:
    Practical and efficient entry to isoflavones by Pd(0)/C-mediated Suzuki–Miyaura reaction. Total synthesis of geranylated isoflavones
    摘要:
    A scalable synthesis of isoflavones taking advantage of the Suzuki-Miyaura reaction catalyzed by Pd(0)/C is described. The approach developed has been extended to the total synthesis of 7-O-geranylformononetin, griffonianone D, and conrauinone D, which did not display cytotoxicity against human HeLa carcinoma cells. In addition, this study established unambiguously the absolute configuration of natural griffonianone D. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2007.01.062
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文献信息

  • Practical and efficient entry to isoflavones by Pd(0)/C-mediated Suzuki–Miyaura reaction. Total synthesis of geranylated isoflavones
    作者:François-Xavier Felpin、Cécile Lory、Hawaa Sow、Samir Acherar
    DOI:10.1016/j.tet.2007.01.062
    日期:2007.4
    A scalable synthesis of isoflavones taking advantage of the Suzuki-Miyaura reaction catalyzed by Pd(0)/C is described. The approach developed has been extended to the total synthesis of 7-O-geranylformononetin, griffonianone D, and conrauinone D, which did not display cytotoxicity against human HeLa carcinoma cells. In addition, this study established unambiguously the absolute configuration of natural griffonianone D. (c) 2007 Elsevier Ltd. All rights reserved.
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