1,4,2-Dithiazole
Chemical compound
From Wikipedia, the free encyclopedia
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;[1] for instance thiocarbonyls via a 1,3-dipolar cycloaddition reaction.[2] These compounds may be protonated by strong acids to give synthetically useful aromatic cations.[3]
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| Names | |
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| Preferred IUPAC name
5H-1,4,2-Dithiazole | |
| Identifiers | |
3D model (JSmol) |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C2H3NS2 | |
| Molar mass | 105.17 g·molâ1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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