5-溴戊氧基苯
| 5-溴戊氧基苯 | |
|---|---|
| |
| 别名 | 5-溴戊基苯基醚 |
| 识别 | |
| CAS号 | 22921-72-8 
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| SMILES |
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| 性质 | |
| 化学式 | C11H15BrO |
| 摩尔质量 | 243.14 g·mol−1 |
| 沸点 | 160~165 °C（11 mmHg）[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
5-溴戊氧基苯是一种有机化合物，化学式为C11H15BrO。它可由苯酚和1,5-二溴戊烷在碳酸钾存在下于二甲基甲酰胺中反应制得。[2]它在苯中和三苯基膦反应，可以得到(5-苯氧基戊基)三苯基𬭸溴化物。[3]
参考文献
[编辑]- ^ 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.