4-氰基苯甲醛肟
4-氰基苯甲醛肟是一种有机化合物，化学式为C8H6N2O。它可由4-氰基苯甲醛和盐酸羟胺在碱的存在下反应得到。[2][3]它和N-氯代丁二酰亚胺在二甲基甲酰胺中反应，可以得到α-氯-4-氰基苯甲醛肟。[2]
| 4-氰基苯甲醛肟 | |
|---|---|
| |
| 英文名 | 4-Cyanobenzaldoxime |
| 别名 | 对氰基苯甲醛肟 |
| 识别 | |
| CAS号 | 64847-77-4 
|
| 性质 | |
| 化学式 | C8H6N2O |
| 摩尔质量 | 146.15 g·mol−1 |
| 熔点 | 174—176 °C（447—449 K）[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
参考文献
编辑- ^ Lin-hua Zhang, J. C. Chung, T. D. Costello, I. Valvis, P. Ma, S. Kauffman, R. Ward. The Enantiospecific Synthesis of an Isoxazoline. A RGD Mimic Platelet GPIIb/IIIa Antagonist. The Journal of Organic Chemistry. 1997-04-01, 62 (8): 2466–2470 [2022-01-16]. ISSN 0022-3263. doi:10.1021/jo9612537 （英语）.
- ^ 2.0 2.1 Laura Schwarz, Ulrich Girreser, Bernd Clement. Synthesis and Characterization of para -Substituted N , N′- Dihydroxybenzamidines and Their Derivatives as Model Compounds for a Class of Prodrugs: para -Substituted N , N′- Dihydroxybenzamidines as Model Prodrugs. European Journal of Organic Chemistry. 2014-03, 2014 (9): 1961–1975 [2022-01-16]. doi:10.1002/ejoc.201301622 （英语）.
- ^ Javad Mokhtari, Mohammad R. Naimi-Jamal, Hamideh Hamzeali, Mohammad G. Dekamin, Gerd Kaupp. Kneading Ball-Milling and Stoichiometric Melts for the Quantitative Derivatization of Carbonyl Compounds with Gas-Solid Recovery. ChemSusChem. 2009-03-23, 2 (3): 248–254 [2022-01-16]. doi:10.1002/cssc.200800258 （英语）.