2-氨基苯並噻唑
2-氨基苯並噻唑 | |
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識別 | |
CAS號 | 136-95-8 |
性質 | |
化學式 | C7H6N2S |
摩爾質量 | 150.2 g·mol−1 |
外觀 | 無色晶體[1] |
密度 | 1.482 g·cm-3(173 K)[1] |
熔點 | 129~130 °C[2] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
2-氨基苯並噻唑是一種有機硫化合物,化學式為C7H6N2S。它可由苯胺、硫氰酸銨和溴在乙酸中反應得到。[2]它和碘甲烷在乙腈中反應,可以得到2-氨基-3-甲基苯並噻唑鎓碘化物。[3]它和氯乙醯氯在碳酸鉀存在下於氯仿中反應,可以得到2-(氯乙醯氨基)苯並噻唑。[4]
參考文獻
- ^ 1.0 1.1 Altaf, Muhammad; Stoeckli-Evans, Helen. 1,3-Benzothiazol-2-amine. Acta Crystallographica, Section E: Structure, 2009. 65 (8): o1894. doi:10.1107/s1600536809027561.
- ^ 2.0 2.1 Li, Huihong; Li, Jing; Chen, Hongxia; Zhang, Yong; Huang, Dan. Synthesis and Crystal Structure of Charge Transfer Complex (CTC) of 2-Aminobenzothiazole with Its Schiff Base. Journal of Chemical Crystallography, 2011. 41 (12): 1844-1849. doi:10.1007/s10870-011-0185-5.
- ^ Meguellati, Kamel; Spichty, Martin; Ladame, Sylvain. Reversible synthesis and characterization of dynamic imino analogues of trimethine and pentamethine cyanine dyes. Organic Letters, 2009. 11 (5): 1123-1126. doi:10.1021/ol802913b.
- ^ Ibrahim, Hamada Mohamed ; Behbehani, Haider. The first Q-Tube based high-pressure synthesis of anti-cancer active thiazolo[4,5-c]pyridazines via the [4 + 2] cyclocondensation of 3-oxo-2-arylhydrazonopropanals with 4-thiazolidinones. Sci. Rep. 2020. 10 (1). doi:10.1038/s41598-020-63453-2.