(3,4,5-Trimethoxy-phenyl)-[3-(3,4,5-trimethoxy-phenyl)-oxiranyl]-methanone | 851729-16-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (3,4,5-Trimethoxy-phenyl)-[3-(3,4,5-trimethoxy-phenyl)-oxiranyl]-methanone
• 英文别名: (3,4,5-Trimethoxyphenyl)-[3-(3,4,5-trimethoxyphenyl)oxiran-2-yl]methanone
• CAS: 851729-16-3
• 化学式: C₂₁H₂₄O₈
• 分子量: 404.417
• InChiKey: YENHNENZZPYNBU-UHFFFAOYSA-N

物化性质

• 熔点：
  83 °C
• 沸点：
  532.2±50.0 °C(Predicted)
• 密度：
  1.227±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  29
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  85
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  (3,4,5-Trimethoxy-phenyl)-[3-(3,4,5-trimethoxy-phenyl)-oxiranyl]-methanone 在 一水合肼 作用下， 以 乙醇 为溶剂， 生成 3,5-bis(3,4,5-trimethoxyphenyl)-4-hydroxy-4,5-dihydro-1H-pyrazole
  参考文献：
  名称：

  Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents

  摘要：

  A series of substituted chalcones and their corresponding pyrazoles were synthesized and evaluated for in vitro cytotoxic activity against a panel of human cancer cell lines. Out of 93 compounds screened, 8 compounds, 1s, 3i,j,n, 4i,j,n and 4s, showed marked activity. Compounds 4j,n and 4s were found to be the most promising in this study. SAR is also discussed. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.03.121
• 作为产物：
  描述：

  1,3-bis(3,4,5-trimethoxyphenyl)propenone 在 sodium hydroxide 、 双氧水 作用下， 以 乙醇 、 水 为溶剂， 反应 15.0h， 生成 (3,4,5-Trimethoxy-phenyl)-[3-(3,4,5-trimethoxy-phenyl)-oxiranyl]-methanone
  参考文献：
  名称：

  Synthesis of 3,5‐Diphenyl‐1H‐Pyrazoles

  摘要：

  An efficient and convenient synthesis of 3,5-diphenyl-IH-pyrazoles from chalcones by the action of hydrazine hydrate on chalcone-epoxide followed by simultaneous dehydration is reported.

  DOI：

  10.1081/scc-200054225

文献信息

• Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents
  作者：B.A. Bhat、K.L. Dhar、S.C. Puri、A.K. Saxena、M. Shanmugavel、G.N. Qazi

  DOI：10.1016/j.bmcl.2005.03.121

  日期：2005.6

  A series of substituted chalcones and their corresponding pyrazoles were synthesized and evaluated for in vitro cytotoxic activity against a panel of human cancer cell lines. Out of 93 compounds screened, 8 compounds, 1s, 3i,j,n, 4i,j,n and 4s, showed marked activity. Compounds 4j,n and 4s were found to be the most promising in this study. SAR is also discussed. (c) 2005 Elsevier Ltd. All rights reserved.
• Synthesis of 3,5‐Diphenyl‐1<i>H</i>‐Pyrazoles
  作者：B. A. Bhat、S. C. Puri、M. A. Qurishi、K. L. Dhar、G. N. Qazi

  DOI：10.1081/scc-200054225

  日期：2005.4.1

  An efficient and convenient synthesis of 3,5-diphenyl-IH-pyrazoles from chalcones by the action of hydrazine hydrate on chalcone-epoxide followed by simultaneous dehydration is reported.