1,3,5-苯三甲醛
| 1,3,5-苯三甲醛 | |
|---|---|
| |
| 别名 | 1,3,5-三甲酰基苯 |
| 识别 | |
| CAS号 | 3163-76-6 
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| SMILES |
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| 性质 | |
| 化学式 | C9H6O3 |
| 摩尔质量 | 162.14 g·mol−1 |
| 熔点 | 160 °C[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
1,3,5-苯三甲醛是一种有机化合物，化学式为C9H6O3。它可由均苯三甲酸酯化后经氢化铝锂还原、氯铬酸吡啶氧化制得。[2]它和丙二腈在催化下反应，可以得到1,3,5-三(2,2-二氰基乙烯基)苯。[3]
参考文献
[编辑]- ^ AL-Saleh, Balkis; Makhseed, Saad; Hassaneen, Huwaida M.; Elnagdi, Mohamed Hilmy (2006). Studies with Functionally Substituted Enamines: The Reactivity of Enaminals and Enamino Esters toward Naphthoquinone, Hydrazonoyl Halides, Aminoazoles and Hippuric Acid. Synthesis, 2006(1), 59–62. doi:10.1055/s-2005-921750.
- ^ Linyi Bai; et al. Nanoscale covalent organic frameworks as smart carriers for drug delivery. Chem. Commun., 2016, 52, 4128-4131. doi:10.1039/C6CC00853D.
- ^ Kai-Yu Cheng, Shi-Cheng Wang, Yu-Sheng Chen, and Yi-Tsu Chan. Self-Assembly and Catalytic Reactivity of BINOL-Bridged Bis(phenanthroline) Metallocages. Inorg. Chem. 2018, 57, 7, 3559–3567. doi:10.1021/acs.inorgchem.7b02540.