1,4,5-萘三酚
| 1,4,5-萘三酚 | |
|---|---|
| |
| 识别 | |
| CAS号 | 481-40-3 
|
| 性质 | |
| 化学式 | C10H8O3 |
| 摩尔质量 | 176.17 g·mol−1 |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
1,4,5-萘三酚是一种有机化合物，化学式为C10H8O3。它可由5-羟基-1,4-萘醌和连二亚硫酸钠反应制得。[1]它可以被二(三氟乙酸)碘苯氧化为5-羟基-1,4-萘醌。[2]它和乙酸酐反应，可以得到1,4,5-萘三酚三乙酸酯。[3]
参考文献
- ^ Na Bao, Jinfeng Ou, Wei Shi, Na Li, Li Chen, Jianbo Sun. Highly Efficient Synthesis and Structure-Activity Relationships of a Small Library of Substituted 1,4-Naphthoquinones: Highly Efficient Synthesis and Structure-Activity Relationships of a Small Library of Substituted 1,4-Naphthoquinones. European Journal of Organic Chemistry. 2018-05-24, 2018 (19): 2254–2258 [2021-11-20]. doi:10.1002/ejoc.201800207 （英语）.
- ^ Robert M. Moriarty, Om Prakash. John Wiley & Sons, Inc. , 编. Oxidation of Phenolic Compounds with Organohypervalent Iodine Reagents. Hoboken, NJ, USA: John Wiley & Sons, Inc. 2001-05-18: 327–415 [2021-11-20]. ISBN 9780471264187. doi:10.1002/0471264180.or057.02. （原始内容存档于2021-11-20） （英语）.
- ^ Mario C. Foti, Erin R. Johnson, Melinda R. Vinqvist, James S. Wright, L. Ross C. Barclay, K. U. Ingold. Naphthalene Diols: A New Class of Antioxidants Intramolecular Hydrogen Bonding in Catechols, Naphthalene Diols, and Their Aryloxyl Radicals. The Journal of Organic Chemistry. 2002-07-01, 67 (15): 5190–5196 [2021-11-20]. ISSN 0022-3263. doi:10.1021/jo020184v. （原始内容存档于2021-11-20） （英语）.