(Z)-5-Ethyl-decenoate | 105986-60-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: (Z)-5-Ethyl-decenoate
• CAS: 105986-60-5
• 化学式: C₁₂H₂₂O₂
• 分子量: 198.305
• InChiKey: ZLJKAHMWTMWHMV-FPLPWBNLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.47
• 重原子数：
  14.0
• 可旋转键数：
  8.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  26.3
• 氢给体数：
  0.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  (Z)-5-Ethyl-decenoate 在 吡啶 、 氢氧化钾 、 草酰氯 、 水 、 N,N-二甲基甲酰胺 作用下， 以 乙醚 、 甲苯 为溶剂， 反应 3.5h， 生成 (Z)-5-Decenoic acid anhydride
  参考文献：
  名称：

  Bioisosteric Approach to Elucidation of Binding of the Acetate Group of a Moth Sex Pheromone Component to Its Receptor

  摘要：

  A number of analogs of (Z)-5-decenyl acetate, a pheromone component of the turnip moth, Agrotis segetum, in which the acetate group has been replaced by functional groups that may function as bioisosters, have been synthesized and tested using single-cell electrophysiology. The activities have been interpreted in terms of the molecular electrostatic potentials of the polar functional group as calculated by ab initio quantum mechanical calculations. It is concluded that both oxygens of the acetate group in (Z)-5-decenyl acetate contribute to the interactions between the pheromone component and its receptor. Furthermore, the results indicate that the crucial interaction between the carbonyl group and the receptor, which is most probably a hydrogen bonding interaction, takes place in a direction pointing away from the hydrocarbon chain of the pheromone component.

  DOI：

  10.1023/a:1022563010599
• 作为产物：
  描述：

  (Z)-1-iodohex-1-ene 、 γ-(Iodzinkio)buttersaeureethylester 在 四(三苯基膦)钯 作用下， 以 N,N-二甲基乙酰胺 、 苯 为溶剂， 反应 0.5h， 以89%的产率得到(Z)-5-Ethyl-decenoate
  参考文献：
  名称：

  Arylation and vinylation of 2-carboethoxyethylzinc iodide and 3-carboethoxypropylzinc iodide catalyzed by palladium

  摘要：

  DOI：

  10.1016/s0040-4039(00)84147-7