Structure via PubChem · Public domain (PubChem)
1,4,2-Dithiazole
Sign in to save1,4,2-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; for instance thiocarbonyls via a 1,3-dipolar cycloaddition reaction. These compounds may be protonated by strong acids to give synthetically useful aromatic cations.
Chemical data
- Formula
- C2H3NS2
- Molecular weight
- 105.19 g/mol
- IUPAC name
- 1,4,2-dithiazole
- SMILES
- C1SC=NS1
- InChIKey
- MNNJLAZJQBWSST-UHFFFAOYSA-N
- XLogP
- 1.1
- Polar surface area
- 63 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 104.970691
Show 2 more facts
- canonical SMILES
- C1SC=NS1
- chemical formula
- C₂H₃NS₂
Sources (1)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
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; for instance thiocarbonyls via a 1,3-dipolar cycloaddition reaction. These compounds may be protonated by strong acids to give synthetically useful aromatic cations.
==References==
Excerpted from Wikipedia’s “1,4,2-Dithiazole” article, available under the CC BY-SA 4.0 licence.