(E)-3-(4-tetradecyloxyphenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one | 1217106-34-7

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 英文名称: (E)-3-(4-tetradecyloxyphenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one
• CAS: 1217106-34-7
• 化学式: C₂₉H₄₀O₃
• 分子量: 436.635
• InChiKey: PVOXNDJAXJMBOG-XQNSMLJCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.37
• 重原子数：
  32.0
• 可旋转键数：
  17.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  46.53
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  (E)-3-(4-tetradecyloxyphenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one 在 六氯环三磷腈 、 potassium carbonate 作用下， 以 丙酮 为溶剂， 反应 1.0h， 以50%的产率得到
  参考文献：
  名称：

  Synthesis and Characterization of Cyclotriphosphazenes Bearing Chalcones Derivatives

  摘要：

  A series of new cyclotriphosphazenes bearing chalcones derivatives, N3P3Cl5[OC6H4 CH=CHC(O)C6H4OCnH2n+1] and N3P3[OC6H4CH=CHC(O)C6H4OCnH2n+1]6, has been synthesized. A convenient synthetic method was performed from the reaction of hexachlorocyclotriphosphazenes with one and six equivalents of (E)-3-(4-(alkyloxy)phenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one (2a-c). The compounds differ in the length of alkyl groups, CnH2n+1, where n = 10, 12, and 14, respectively. All the products were obtained in high yields. The structures of the synthesized compounds were defined by elemental analysis, IR, 1H, 13C, and 31P NMR.

  DOI：

  10.1080/10426500902893217
• 作为产物：
  描述：

  4-(十四烷氧基)苯甲醛 、 对羟基苯乙酮 在 potassium hydroxide 作用下， 以 甲醇 为溶剂， 反应 10.0h， 以54%的产率得到(E)-3-(4-tetradecyloxyphenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one
  参考文献：
  名称：

  Synthesis and Characterization of Cyclotriphosphazenes Bearing Chalcones Derivatives

  摘要：

  A series of new cyclotriphosphazenes bearing chalcones derivatives, N3P3Cl5[OC6H4 CH=CHC(O)C6H4OCnH2n+1] and N3P3[OC6H4CH=CHC(O)C6H4OCnH2n+1]6, has been synthesized. A convenient synthetic method was performed from the reaction of hexachlorocyclotriphosphazenes with one and six equivalents of (E)-3-(4-(alkyloxy)phenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one (2a-c). The compounds differ in the length of alkyl groups, CnH2n+1, where n = 10, 12, and 14, respectively. All the products were obtained in high yields. The structures of the synthesized compounds were defined by elemental analysis, IR, 1H, 13C, and 31P NMR.

  DOI：

  10.1080/10426500902893217