1,3,5-三甲氧基苯
化合物
1,3,5-三甲氧基苯是一种有机化合物，化学式为C9H12O3。它可由1,3,5-三溴苯和甲醇钠在氯化亚铜、甲酸甲酯催化下反应制得。[3]它和N-溴代丁二酰亚胺在四氯化碳中反应，可以得到2-溴-1,3,5-三甲氧基苯。[4]它可用作核磁共振氢谱的内标。[5]
| 1,3,5-三甲氧基苯 | |
|---|---|
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| 识别 | |
| CAS号 | 621-23-8 
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| 性质 | |
| 化学式 | C9H12O3 |
| 摩尔质量 | 168.19 g·mol−1 |
| 外观 | 白色晶体[1] |
| 熔点 | 53—54 °C（326—327 K）[1] |
| 沸点 | 147 °C（420 K）（2.5 torr）[2] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
参考文献
- ^ 1.0 1.1 Qian Wang, Jian Yang, Yang Zheng, Xiali Liao. An Alternative Synthesis of 2,6-Dimethoxyl-1,4-Benzoquinone. Journal of Chemical Research. 2017-04, 41 (4): 193–194 [2023-04-03]. ISSN 1747-5198. doi:10.3184/174751917X14894997017379 （英语）.
- ^ Maillard, Jacques; Vincent, Michel; Delaunay, Pierre; Fumeron, Bernard. Derivatives of phloroglucinol. I. Synthesis and acetylation of mono-, di-, and triethers of mono- and dichloro-2,4,6-trihydroxybenzoic acid. Bulletin de la Societe Chimique de France, 1966. 8: 2520-2524.
- ^ Ying Guo, Si-Zhe Ji, Cheng Chen, Hong-Wei Liu, Jian-Hong Zhao, Yu-Lin Zheng, Ya-Fei Ji. A ligand-free, powerful, and practical method for methoxylation of unactivated aryl bromides by use of the CuCl/HCOOMe/MeONa/MeOH system. Research on Chemical Intermediates. 2015-11, 41 (11): 8651–8664 [2023-04-03]. ISSN 0922-6168. doi:10.1007/s11164-014-1917-x （英语）.
- ^ Mukulesh Mondal, Vedavati G. Puranik, Narshinha P. Argade. Facile Synthesis of 1,3,7-Trihydroxyxanthone and Its Regioselective Coupling Reactions with Prenal: Simple and Efficient Access to Osajaxanthone and Nigrolineaxanthone F. The Journal of Organic Chemistry. 2006-06-01, 71 (13): 4992–4995 [2023-04-03]. ISSN 0022-3263. doi:10.1021/jo0606655. （原始内容存档于2021-06-12） （英语）.
- ^ Ruslan Muhamadejev, Renate Melngaile, Paula Paegle, Ieva Zibarte, Marina Petrova, Kristaps Jaudzems, Janis Veliks. Residual Solvent Signal of CDCl 3 as a qNMR Internal Standard for Application in Organic Chemistry Laboratory. The Journal of Organic Chemistry. 2021-03-05, 86 (5): 3890–3896 [2023-04-03]. ISSN 0022-3263. doi:10.1021/acs.joc.0c02744. （原始内容存档于2021-11-19） （英语）.