4-氰基苯甲醛肟
4-氰基苯甲醛肟是一種有機化合物，化學式為C8H6N2O。它可由4-氰基苯甲醛和鹽酸羥胺在鹼的存在下反應得到。[2][3]它和N-氯代丁二醯亞胺在二甲基甲醯胺中反應，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 |
| 別名 | 對氰基苯甲醛肟 |
| 識別 | |
| CAS號 | 64847-77-4 
|
| 性質 | |
| 化學式 | C8H6N2O |
| 摩爾質量 | 146.15 g·mol−1 |
| 熔點 | 174—176 °C（447—449 K）[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
參考文獻
編輯- ^ 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 （英語）.
- ^ 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 （英語）.
- ^ 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 （英語）.