1,3,5-苯三甲醛
| 1,3,5-苯三甲醛 | |
|---|---|
| |
| 別名 | 1,3,5-三甲酰基苯 |
| 識別 | |
| CAS號 | 3163-76-6 
|
| SMILES |
|
| 性質 | |
| 化學式 | C9H6O3 |
| 摩爾質量 | 162.14 g·mol−1 |
| 熔點 | 160 °C[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
1,3,5-苯三甲醛是一種有機化合物，化學式為C9H6O3。它可由均苯三甲酸酯化後經氫化鋁鋰還原、氯鉻酸吡啶氧化製得。[2]它和丙二腈在催化下反應，可以得到1,3,5-三(2,2-二氰基乙烯基)苯。[3]
參考文獻
- ^ 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.