Thiazole

Thiazole
Names
	Preferred IUPAC name 1,3-Thiazole
	Other names Thiazole
Identifiers
CAS Number	288-47-1 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:43732 ;
ChEMBL	ChEMBL15605 ;
ChemSpider	8899 ;
ECHA InfoCard	100.005.475
PubChem CID	9256;
UNII	320RCW8PEF ;
CompTox Dashboard (EPA)	DTXSID2059776 ;
	InChI InChI=1S/C3H3NS/c1-2-5-3-4-1/h1-3H Key: FZWLAAWBMGSTSO-UHFFFAOYSA-N ; InChI=1/C3H3NS/c1-2-5-3-4-1/h1-3H Key: FZWLAAWBMGSTSO-UHFFFAOYAI;
	SMILES n1ccsc1;
Properties
Chemical formula	C3H3NS
Molar mass	85.12 g·mol−1
Boiling point	116 to 118 °C (241 to 244 °F; 389 to 391 K)
Acidity (pKa)	2.5 (of conjugate acid)
Magnetic susceptibility (χ)	-50.55·10−6 cm3/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Thiazole (/ˈθaɪ.əzoʊl/), or 1,3-thiazole, is a 5-membered heterocyclic compound that contains both sulfur and nitrogen. The term 'thiazole' also refers to a large family of derivatives. Thiazole itself is a pale yellow liquid with a pyridine-like odor and the molecular formula C₃H₃NS.^[2] The thiazole ring is notable as a component of the vitamin thiamine (B₁).

^ Zoltewicz, J. A.; Deady, L. W. (1978). "Quaternization of Heteroaromatic Compounds: Quantitative Aspects". Advances in Heterocyclic Chemistry Volume 22. Vol. 22. pp. 71–121. doi:10.1016/S0065-2725(08)60103-8. ISBN 9780120206223.
^ Eicher, T.; Hauptmann, S. (2003). The Chemistry of Heterocycles: Structure, Reactions, Syntheses, and Applications. Wiley. ISBN 978-3-527-30720-3.

[1] Zoltewicz, J. A.; Deady, L. W. (1978). "Quaternization of Heteroaromatic Compounds: Quantitative Aspects". Advances in Heterocyclic Chemistry Volume 22. Vol. 22. pp. 71–121. doi:10.1016/S0065-2725(08)60103-8. ISBN 9780120206223.

[2] Eicher, T.; Hauptmann, S. (2003). The Chemistry of Heterocycles: Structure, Reactions, Syntheses, and Applications. Wiley. ISBN 978-3-527-30720-3.

[1]

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Thiazole

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