1,4,2-Dithiazole

changed 477205645 1,4,2-Dithiazole.svg 100px 5H-1,4,2-Dithiazole 289-12-3 correct FDA 9Z36GFK3RQ 21943157 correct chemspider 11438410 correct chemspider 1S/C2H3NS2/c1-3-5-2-4-1/h1H,2H2 correct chemspider MNNJLAZJQBWSST-UHFFFAOYSA-N C1SC=NS1 2 3 1 2 1,4,2-Dithiazole is a heterocyclic compound consisting of an unsaturated five-membered ring containing two carbon atoms, one nitrogen atom, and two sulfur atoms. 1,4,2-Dithiazole compounds may be formed by the reaction of nitrile sulfide (formed by the thermolysis of oxathiazolone) with various reactive species;Argyropoulos Nikolaos G. 1,4-Oxa/thia-2-azoles 1996 491–543 Comprehensive Heterocyclic Chemistry II 10.1016/B978-008096518-5.00092-7 978-0-08-096518-5 for instance thiocarbonyls via a 1,3-dipolar cycloaddition reaction.Wai Kwok-Fai Sammes Michael P. Dithiazoles and related compounds. Part 3. Preparation of 5H-1,4,2-dithiazoles via 1,3-dipolar cycloadditions between nitrile sulphides and thiocarbonyl compounds, and some conversions into 3,5-diaryl-1,4,2-dithiazolium salts Journal of the Chemical Society, Perkin Transactions 1 1 1991 183 0300-922X 10.1039/p19910000183 These compounds may be protonated by strong acids to give synthetically useful aromatic cations.Wai Kwok-Fai Sammes Michael P. Dithiazoles and related compounds. Part. 4. Preparation of 1,4,2-dithiazolium salts unsubstituted at C-5 including the parent heterocycle, NMR spectroscopic evidence for aromaticity, and some novel reactions Journal of the Chemical Society, Perkin Transactions 1 16 1992 2065 0300-922X 10.1039/p19920002065 References Category:Nitrogen heterocycles Category:Sulfur heterocycles Category:Sulfur–nitrogen compounds Category:Organic compounds with 2 carbon atoms