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 thermolysisofoxathiazolone) 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]
![]() | |
Names | |
---|---|
Preferred IUPAC name
5H-1,4,2-Dithiazole | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider |
|
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C2H3NS2 | |
Molar mass | 105.17 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it. |