3(2H)-苯并呋喃酮
| 3(2H)-苯并呋喃酮 | |
|---|---|
| |
| 别名 | 3-苯并呋喃酮 |
| 识别 | |
| CAS号 | 7169-34-8 
|
| 性质 | |
| 化学式 | C8H6O2 |
| 摩尔质量 | 134.13 g·mol−1 |
| 熔点 | 101 °C[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
3(2H)-苯并呋喃酮是一种有机化合物，化学式为C8H6O2，它可由乙酸苯并呋喃-3-酯在盐酸-甲醇中回流制得。[2]它可以被硼氢化钠在甲醇中还原为2,3-二氢-3-苯并呋喃醇。[3]
参考文献
- ^ Deshpande, A. R.; Paradkar, M. V. Synthesis of 3-(3-Benzofuranyl)coumarins. Synthetic Communications (Informa UK Limited). 1990, 20 (6): 809–816. ISSN 0039-7911. doi:10.1080/00397919008052326.
- ^ Venkatesan, Aranapakam M.; Dos Santos, O.; Ellingboe, John; Evrard, Deborah A.; Harrison, Boyd L.; Smith, Deborah L.; Scerni, Rosemary; Hornby, Geoffrey A.; Schechter, Lee E.; Andree, Terrence H. Novel benzofuran derivatives with dual 5-HT1A receptor and serotonin transporter affinity. Bioorganic & Medicinal Chemistry Letters (Elsevier BV). 2010, 20 (3): 824–827. ISSN 0960-894X. doi:10.1016/j.bmcl.2009.12.093.
- ^ Chen, Kang; Schwarz, Johanna; Karl, Tobias A.; Chatterjee, Anamitra; König, Burkhard. Visible light induced redox neutral fragmentation of 1,2-diol derivatives. Chemical Communications (Royal Society of Chemistry (RSC)). 2019, 55 (87): 13144–13147. ISSN 1359-7345. doi:10.1039/c9cc06904f.