Aminothiazole
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| Names | |
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| Preferred IUPAC name
1,3-Thiazol-2-amine | |
| Other names
2-Thiazolamine, Aminothiazole, 2-Thiazylamine, Basedol, 2-Thiazolylamine, 4-Thiazolin-2-onimine, 2-Amino-1,3-thiazole, Abadole
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| Identifiers | |
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3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.284 
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| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C3H4N2S | |
| Molar mass | 100.14 g·mol−1 |
| Appearance | Light yellow crystals |
| Melting point | 86 to 89 °C (187 to 192 °F; 359 to 362 K) |
| Boiling point | 117 °C (243 °F; 390 K) (20 hPa) |
| 100 g/l (20 °C) | |
| -56.0·10−6 cm3/mol | |
| Hazards | |
| NFPA 704 (fire diamond) | 
2
0
0 |
| 600 °C (1,112 °F; 873 K) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
2-Aminothiazole is a heterocyclic amine featuring a thiazole core. It can also be considered a cyclic isothiourea. It possesses an odor similar to pyridine and is soluble in water, alcohols and diethyl ether. It is commonly used as a starting point for the synthesis of many compounds including sulfur drugs, biocides, fungicides, dyes and chemical reaction accelerators. 2-Aminothiazole can be used as a thyroid inhibitor in the treatment of hyperthyroidism and has antibacterial activity. Alternatively, its acid tartrate salt can be used. Recent studies using prion-infected neuroblastoma cell lines have suggested that aminothiazole may be used as a therapeutic drug for prion diseases.[1]
2-Aminothiazole is used in the synthesis of vosaroxin.[citation needed]
References[]
- ^ Gallardo-Godoy A; Gever J; Fife KL; Silber BM; Prusiner SB; Renslo AR. (Feb 24, 2011). "2-Aminothiazoles as therapeutic leads for prion diseases". J Med Chem. 54 (4): 1010–21. doi:10.1021/jm101250y. PMC 3041857. PMID 21247166.
- Amines
- Thiazoles