4-溴吡啶
| 4-溴吡啶 | |
|---|---|
| |
| 识别 | |
| CAS号 | 1120-87-2 
|
| 性质 | |
| 化学式 | C5H4BrN |
| 摩尔质量 | 158 g·mol−1 |
| 熔点 | 6 °C[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
4-溴吡啶是一种有机化合物，化学式为C5H4BrN。它可由4-氨基吡啶的重氮化反应制得。[2]它和2-溴吡啶（锂化后处理为有机锌试剂）在钯配合物的催化锌进行根岸偶联反应，可以制得2,4'-联吡啶。[3]
参考文献
[编辑]- ^ Cumper, Charles W. N.; Vogel, Arthur I. 920. Physical properties and chemical constitution. Part XXX. The dipole moments of some halogeno- and cyano-pyridines. Journal of the Chemical Society (Resumed). 1960: 4723. ISSN 0368-1769. doi:10.1039/jr9600004723.
- ^ Murray, Arthur; Langham, Wright H. A Synthesis of Isonicotinic Acid by Halogen—Metal Exchange and Its Application to the Preparation of Isonicotinic-C14Acid Hydrazide1. Journal of the American Chemical Society. 1952, 74 (24): 6289–6290. ISSN 0002-7863. doi:10.1021/ja01144a515.
- ^ Sidler, Daniel R; Barta, Nancy; Li, Wenjie; Hu, Essa; Matty, Louis; Ikemoto, Nori; Campbell, Jeffrey S; Chartrain, Michel; Gbewonyo, Kozo; Boyd, Russell; Corley, Edward G; Ball, Richard G; Larsen, Robert D; Reider, Paul J. Efficient synthesis of the optically active dihydropyrimidinone of a potent α1A- selective adrenoceptor antagonist. Canadian Journal of Chemistry. 2002, 80 (6): 646–652. ISSN 0008-4042. doi:10.1139/v02-079.
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.
Cover photo is available under {{::mainImage.info.license.name || 'Unknown'}} license.
Cover photo is available under {{::mainImage.info.license.name || 'Unknown'}} license.
Credit:
(see original file).
