5-iodo-2,2-dimethyl-10-phenyl-2H,8H-pyrano[2,3-f]chromen-8-one | 1185741-04-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 新黄酮类化合物
• 英文名称: 5-iodo-2,2-dimethyl-10-phenyl-2H,8H-pyrano[2,3-f]chromen-8-one
• 英文别名: 5-Iodo-2,2-dimethyl-10-phenylpyrano[2,3-f]chromen-8-one
• CAS: 1185741-04-1
• 化学式: C₂₀H₁₅IO₃
• 分子量: 430.242
• InChiKey: IJJBULKYHVPJDL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  24
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  5-iodo-2,2-dimethyl-10-phenyl-2H,8H-pyrano[2,3-f]chromen-8-one 、 噻吩-1-硼酸 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 cesium fluoride 作用下， 以 1,4-二氧六环 为溶剂， 以76.4%的产率得到5-[thianthren-1-yl]-2,2-dimethyl-10-phenyl-2H,8H-pyrano[2,3-f]chromen-8-one
  参考文献：
  名称：

  Synthesis and evaluation of novel substituted 5-hydroxycoumarin and pyranocoumarin derivatives exhibiting significant antiproliferative activity against breast cancer cell lines

  摘要：

  A library of novel 5-hydroxycoumarin and pyranocoumarin derivatives was constructed via silica sulfuric acid-catalyzed pechmann reaction and Pd(0)-catalyzed suzuki coupling in tandem, and their antiproliferative activities against breast cancer cells MCF-7 and MDA-MB-231 were evaluated. The results showed that compounds such as 6b, 6d, 6h, and 6k possess significant antiproliferative activity against MCF-7 cell line with the IC50 values of 7.2, 5.3, 3.3, and 6.5 mu M, respectively. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.06.098
• 作为产物：
  描述：

  3-甲基-2-丁烯醛 、 5-hydroxy-7-iodo-4-phenyl-2H-chromen-2-one 在 苯硼酸 作用下， 以 丙酸 、 甲苯 为溶剂， 反应 4.0h， 以79.2%的产率得到5-iodo-2,2-dimethyl-10-phenyl-2H,8H-pyrano[2,3-f]chromen-8-one
  参考文献：
  名称：

  Synthesis and evaluation of novel substituted 5-hydroxycoumarin and pyranocoumarin derivatives exhibiting significant antiproliferative activity against breast cancer cell lines

  摘要：

  A library of novel 5-hydroxycoumarin and pyranocoumarin derivatives was constructed via silica sulfuric acid-catalyzed pechmann reaction and Pd(0)-catalyzed suzuki coupling in tandem, and their antiproliferative activities against breast cancer cells MCF-7 and MDA-MB-231 were evaluated. The results showed that compounds such as 6b, 6d, 6h, and 6k possess significant antiproliferative activity against MCF-7 cell line with the IC50 values of 7.2, 5.3, 3.3, and 6.5 mu M, respectively. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.06.098