4-硝基亞苄基丙二腈
| 4-硝基亞苄基丙二腈 | |
|---|---|
| |
| 別名 | 1-(2,2-二氰乙烯基)-4-硝基苯 2-[(4-硝基苯基)亞甲基]丙二腈 |
| 識別 | |
| CAS號 | 2700-23-4 
|
| 性質 | |
| 化學式 | C10H5N3O2 |
| 莫耳質量 | 199.17 g·mol⁻¹ |
| 熔點 | 160 °C（433 K）[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
4-硝基亞苄基丙二腈是一種有機化合物，化學式為C10H5N3O2。它可由4-硝基苯甲醛和丙二腈的Knoevenagel縮合反應製得。[2]它和次氯酸鈣反應，可以得到2,2-二氰基-3-(4-硝基苯基)環氧乙烷。[3]
參考文獻[編輯]
- ^ Saeed Balalaie, Morteza Bararjanian, Shohreh Hekmat, Peyman Salehi. Novel, Efficient, and Green Procedure for the Knoevenagel Condensation Catalyzed by Diammonium Hydrogen Phosphate in Water. Synthetic Communications. 2006-12, 36 (24): 3703–3711 [2021-05-17]. ISSN 0039-7911. doi:10.1080/10916460600946113 （英語）.
- ^ Bhaskar Sarmah, Biswarup Satpati, Rajendra Srivastava. Highly efficient and recyclable basic mesoporous zeolite catalyzed condensation, hydroxylation, and cycloaddition reactions. Journal of Colloid and Interface Science. 2017-05, 493: 307–316 [2021-05-17]. doi:10.1016/j.jcis.2017.01.039 （英語）.
- ^ F. Mirhashemi, M.A. Amrollahi. Epoxidation of vinyl cyanides by calcium hypochlorite under catalyst- and solvent-free conditions. Tetrahedron Letters. 2018-07, 59 (27): 2661–2663 [2021-05-17]. doi:10.1016/j.tetlet.2018.05.077 （英語）.