𫫇唑-4-甲醛

𫫇唑-4-甲醛是一种有机化合物，化学式为C₄H₃NO₂。它可由𫫇唑-4-甲酸乙酯经二异丁基氢化铝还原制得，^[2]或通过𫫇唑-4-甲醇经二氧化锰氧化得到。^[3]它和丙基溴化镁（法语：Bromure de propylmagnésium）反应，可以得到α-丙基𫫇唑-4-甲醇。^[4]

𫫇唑-4-甲醛
别名	4-甲酰基𫫇唑
识别
CAS号	118994-84-6  Y
性质
化学式	C4H3NO2
摩尔质量	97.07 g·mol−1
外观	白色固体[1]
熔点	59—61 °C（332—334 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

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. （原始内容存档于2022-10-07） （英语）.
2. 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. （原始内容存档于2022-10-07） （英语）.
3. 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.
4. 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 （英语）.