Names | |
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Preferred IUPAC name
5H-1,4,2-Dithiazole | |
Identifiers | |
3D model (
JSmol)
|
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ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
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| |
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).
|
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]
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).
|
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]