5-溴戊氧基苯
| 5-溴戊氧基苯 | |
|---|---|
| |
| 別名 | 5-溴戊基苯基醚 |
| 識別 | |
| CAS號 | 22921-72-8 
|
| SMILES |
|
| 性質 | |
| 化學式 | C11H15BrO |
| 摩爾質量 | 243.14 g·mol−1 |
| 沸點 | 160~165 °C（11 mmHg）[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
5-溴戊氧基苯是一種有機化合物，化學式為C11H15BrO。它可由苯酚和1,5-二溴戊烷在碳酸鉀存在下於二甲基甲醯胺中反應製得。[2]它在苯中和三苯基膦反應，可以得到(5-苯氧基戊基)三苯基鏻溴化物。[3]
參考文獻
[編輯]- ^ Peter Gaubert; R. P. Linstead and H. N. Rydon. Investigations of the olefinic acids. Part XVII. The addition of hydrogen bromide to heptenoic and nonenoic acids with terminal double bonds. J. Chem. Soc., 1937, 1974-1979. doi:10.1039/JR9370001974.
- ^ Wang, Wenya; et al. Design, Synthesis, and Antifungal Activity of Novel Conformationally Restricted Triazole Derivatives. Archiv der Pharmazie (Weinheim, Germany) (2009), 342(12), 732-739. doi:10.1002/ardp.200900103.
- ^ Jiang, Shan; et al. Novel Functionalized Cannabinoid Receptor Probes: Development of Exceptionally Potent Agonists. Journal of Medicinal Chemistry (2021), 64(7), 3870-3884. doi:10.1021/acs.jmedchem.0c02053.