2-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)ethenyl]-cyclopent-1-enecarbaldehyde | 189271-20-3

• 分子结构分类: 有机化合物 - 有机氧化合物 - 有机氧化物
• 英文名称: 2-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)ethenyl]-cyclopent-1-enecarbaldehyde
• CAS: 189271-20-3
• 化学式: C₁₇H₂₄O
• 分子量: 244.377
• InChiKey: KSDVESVCIFQVGK-MDZDMXLPSA-N

物化性质

• 沸点：
  366.9±21.0 °C(Predicted)
• 密度：
  1.099±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.75
• 重原子数：
  18.0
• 可旋转键数：
  3.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  17.07
• 氢给体数：
  0.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  2-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)ethenyl]-cyclopent-1-enecarbaldehyde 在 氢氧化钾 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 乙醇 、 正己烷 为溶剂， 反应 1.25h， 生成 (2E,4E)-3-methyl-5-[2-[(E)-2-(2,6,6-trimethylcyclohex-1-en-1-yl)ethenyl]-1-cyclopenten-1-yl]-2,4-pentadienoic acid
  参考文献：
  名称：

  Thrombomodulin induction in cultured human endothelial cells by 9-cis-locked retinoic acid analogues

  摘要：

  9-cis-Retinoic acid (RA) analogues devised to lock the 9-cis double bond by ring formation were synthesized using two stereoselective carbon-carbon bond formation reactions as key steps. The palladium-mediated Suzuki reaction was adopted to construct a 7E-double bond (RA numbering) and the Horner-Emmons olefination was employed for stereoselective 11E-double bond (RA numbering) formation. The synthesized 9-cis-RA analogues that are locked by five-membered ring systems (cyclopentene, dihydrofuran, and dihydrothiophene) were shown to have comparable thrombomodulin induction activities to that of 9-cis RA. Conformational analysis of these compounds showed their similarity to 9-cis RA in the spatial orientation of the side chain and the terminal carboxy group. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2006.04.043
• 作为产物：
  描述：

  2-(三氟甲基磺酰氧基)-1-环戊烯-1-甲酸乙酯 在 四(三苯基膦)钯 manganese(IV) oxide 、 氢氧化钾 、 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 、 水 、 Petroleum ether 、 苯 为溶剂， 反应 5.0h， 生成 2-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)ethenyl]-cyclopent-1-enecarbaldehyde
  参考文献：
  名称：

  Thrombomodulin induction in cultured human endothelial cells by 9-cis-locked retinoic acid analogues

  摘要：

  9-cis-Retinoic acid (RA) analogues devised to lock the 9-cis double bond by ring formation were synthesized using two stereoselective carbon-carbon bond formation reactions as key steps. The palladium-mediated Suzuki reaction was adopted to construct a 7E-double bond (RA numbering) and the Horner-Emmons olefination was employed for stereoselective 11E-double bond (RA numbering) formation. The synthesized 9-cis-RA analogues that are locked by five-membered ring systems (cyclopentene, dihydrofuran, and dihydrothiophene) were shown to have comparable thrombomodulin induction activities to that of 9-cis RA. Conformational analysis of these compounds showed their similarity to 9-cis RA in the spatial orientation of the side chain and the terminal carboxy group. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2006.04.043