4-氰基苯乙腈
| 4-氰基苯乙腈 | |
|---|---|
| 识别 | |
| CAS号 | 876-31-3 
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| SMILES |
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| 性质 | |
| 化学式 | C9H6N2 |
| 摩尔质量 | 142.16 g·mol−1 |
| 熔点 | 96~98 °C[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
4-氰基苯乙腈是一种有机化合物，化学式为C9H6N2。它可由4-氰基溴苄和氰化钠在二甲基亚砜中反应制得。[2]它和苯甲醛在催化下反应，可以得到4-氰基-α-亚苄基苯乙腈。[3]
参考文献
[编辑]- ^ Peter J. Lindsay-Scott; et al. Two-Step Cyanomethylation Protocol: Convenient Access to Functionalized Aryl- and Heteroarylacetonitriles. Org. Lett. 2015, 17, 3, 476–479. doi:10.1021/ol503479g.
- ^ Balasaravanan, Rajendiran; et al. Triphenylamino α-Cyanovinyl- and Cyanoaryl-Based Fluorophores: Solvatochromism, Aggregation-Induced Emission and Electrochemical Properties. Asian Journal of Organic Chemistry (2016), 5(3), 399-410. doi:10.1002/ajoc.201500488.
- ^ Dhevalapally B. Ramachary; M. Shiva Prasad. Direct amino acid-catalyzed cascade reductive alkylation of arylacetonitriles: high-yielding synthesis of ibuprofen analogs. Tetrahedron Letters, 2020. 51 (40). 5246-5251. doi:10.1016/j.tetlet.2010.07.131.