Isothiazole
An isothiazole, or 1,2-thiazole, is a type of organic compound containing a five-membered aromatic ring that consists of three carbon atoms, one nitrogen atom, and one sulfur atom.[4] Isothiazole is a member of a class of compounds known as azoles. In contrast to the isomeric thiazole, the two heteroatoms are in adjacent positions.
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| Names | |||
|---|---|---|---|
| Preferred IUPAC name
 1,2-Thiazole[1]  | |||
| Other names
 isothiazole  | |||
| Identifiers | |||
3D model (JSmol)  | 
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| ChemSpider | |||
| ECHA InfoCard | 100.241.294 | ||
PubChem CID  | 
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| UNII | |||
CompTox Dashboard (EPA)  | 
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| Properties | |||
| C3H3NS | |||
| Molar mass | 85.12 g·mol−1 | ||
| Boiling point | 114 °C (237 °F; 387 K)[2] | ||
| Acidity (pKa) | -0.5 (of conjugate acid)[3] | ||
| Related compounds | |||
Related compounds  | 
thiazole, isoxazole | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 
Infobox references  | |||
The ring structure of isothiazole is incorporated into larger compounds with biological activity such as the pharmaceutical drugs ziprasidone and perospirone.
See also
    
    
References
    
- International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 140. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
 - Isothiazoles, D. W. Brown and M. Sainsbury, page 513
 - Zoltewicz, J. A. & Deady, L. W. Quaternization of heteroaromatic compounds. Quantitative aspects. Adv. Heterocycl. Chem. 22, 71-121 (1978)
 - Heterocyclic Chemistry, 3rd Edition, J.A. Joule, K. Mills, and G.F. Smith, page 394
 
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