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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid [{{fullurl:1,4,2-Dithiazole|oldid=443937220}} 443937220] of page [[1,4,2-Dithiazole]] with values updated to verified values.}}
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| verifiedrevid = 443935604
| verifiedrevid = 477205645
|ImageFile=1,4,2-Dithiazole.svg
| ImageFile=1,4,2-Dithiazole.svg
|ImageSize=100px
| ImageSize=100px
|IUPACName=1,4,2-Dithiazole
| PIN=5''H''-1,4,2-Dithiazole
|OtherNames=
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|Section1={{Chembox Identifiers
|Section1={{Chembox Identifiers
| CASNo=
| CASNo=289-12-3
| UNII_Ref = {{fdacite|correct|FDA}}
| PubChem=21943157
| UNII = 9Z36GFK3RQ
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| PubChem=21943157
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 11438410
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
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|Section2={{Chembox Properties
|Section2={{Chembox Properties
| C=2|H=3|N=1|S=2
| C=2 | H=3 | N=1 | S=2
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|Section3={{Chembox Hazards
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'''1,4,2-Dithiazole''' is a [[heterocyclic compound]] consisting of an [[Saturated and unsaturated compounds|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 [[thermal decomposition|thermolysis]] of [[oxathiazolone]]) with various reactive species;<ref name="Argyropoulos1996">{{cite journal|last1=Argyropoulos|first1=Nikolaos G.|title=1,4-Oxa/thia-2-azoles|year=1996|pages=491–543|journal=Comprehensive Heterocyclic Chemistry II|doi=10.1016/B978-008096518-5.00092-7|ISBN=978-0-08-096518-5 }}</ref> for instance thiocarbonyls via a [[1,3-dipolar cycloaddition]] reaction.<ref>{{cite journal|last1=Wai|first1=Kwok-Fai|last2=Sammes|first2=Michael P.|title=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=Journal of the Chemical Society, Perkin Transactions 1|issue=1|year=1991|pages=183|issn=0300-922X|doi=10.1039/p19910000183}}</ref> These compounds may be protonated by strong acids to give synthetically useful [[Aromaticity|aromatic]] [[cations]].<ref name="WaiSammes1992">{{cite journal|last1=Wai|first1=Kwok-Fai|last2=Sammes|first2=Michael P.|title=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=Journal of the Chemical Society, Perkin Transactions 1|issue=16|year=1992|pages=2065|issn=0300-922X|doi=10.1039/p19920002065}}</ref>

==References==
{{Reflist}}

{{DEFAULTSORT:Dithiazole, 1,4,2-}}
[[Category:Nitrogen heterocycles]]
[[Category:Sulfur heterocycles]]
[[Category:Sulfur–nitrogen compounds]]


{{heterocyclic-stub}}