1,3,5-苯三甲醛
1,3,5-苯三甲醛 | |
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别名 | 1,3,5-三甲酰基苯 |
识别 | |
CAS号 | 3163-76-6 ![]() |
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
- ^ 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.