噁唑-4-甲醛
| 噁唑-4-甲醛 | |
|---|---|
| |
| 別名 | 4-甲酰基噁唑 |
| 識別 | |
| CAS號 | 118994-84-6 
|
| 性質 | |
| 化學式 | C4H3NO2 |
| 摩爾質量 | 97.07 g·mol−1 |
| 外觀 | 白色固體[1] |
| 熔點 | 59—61 °C（332—334 K）[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
噁唑-4-甲醛是一種有機化合物，化學式為C4H3NO2。它可由噁唑-4-甲酸乙酯經二異丁基氫化鋁還原製得，[2]或通過噁唑-4-甲醇經二氧化錳氧化得到。[3]它和丙基溴化鎂反應，可以得到α-丙基噁唑-4-甲醇。[4]
參考文獻
- ^ 1.0 1.1 Jonathan T. Reeves, Jinhua J. Song, Zhulin Tan, Heewon Lee, Nathan K. Yee, Chris H. Senanayake. A General Synthesis of Substituted Formylpyrroles from Ketones and 4-Formyloxazole. Organic Letters. 2007-05-01, 9 (10): 1875–1878 [2022-10-05]. ISSN 1523-7060. doi:10.1021/ol070340q. （原始內容存檔於2022-10-07） （英語）.
- ^ Ivana Šagud, Simona Božić, Željko Marinić, Marija Šindler-Kulyk. Photochemical approach to functionalized benzobicyclo[3.2.1]octene structures via fused oxazoline derivatives from 4- and 5-( o -vinylstyryl)oxazoles. Beilstein Journal of Organic Chemistry. 2014-09-18, 10: 2222–2229 [2022-10-05]. ISSN 1860-5397. doi:10.3762/bjoc.10.230. （原始內容存檔於2022-10-07） （英語）.
- ^ Kajino, Masahiro; Hird, Nicholas William; Tarui, Naoki; Banno, Hiroshi; Kawano, Yasuhiko; Inatomi, Nobuhiro. Preparation of fused quinoline derivatives as NK2 receptor antagonists for functional gastrointestinal diseases. 2005 WO 2005105802 A1.
- ^ Roger J. Mulder, Cynthia M. Shafer, Doralyn S. Dalisay, Tadeusz F. Molinski. Synthesis and structure–activity relationships of bengazole A analogs. Bioorganic & Medicinal Chemistry Letters. 2009-06, 19 (11): 2928–2930 [2022-10-05]. doi:10.1016/j.bmcl.2009.04.069 （英語）.