Sulfathiazole (original) (raw)

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Chemical compound

Pharmaceutical compound

Sulfathiazole

Imino (top) and amino (bottom) tautomers
Clinical data
AHFS/Drugs.com International Drug Names
ATC code D06BA02 (WHO) J01EB07 (WHO) QJ01EQ07 (WHO)
Identifiers
IUPAC name 4-amino-_N_-(1,3-thiazol-2-yl)benzenesulfonamide
CAS Number 72-14-0 checkY
PubChem CID 5340
DrugBank DB06147 checkY
ChemSpider 5148 checkY
UNII Y7FKS2XWQH
KEGG D01047 checkY
ChEBI CHEBI:9337 checkY
ChEMBL ChEMBL437 checkY
CompTox Dashboard (EPA) DTXSID8026068 Edit this at Wikidata
ECHA InfoCard 100.000.701 Edit this at Wikidata
Chemical and physical data
Formula C9H9N3O2S2
Molar mass 255.31 g·mol−1
3D model (JSmol) Interactive image
Melting point 202 to 202.5 °C (395.6 to 396.5 °F)
SMILES O=S(=O)(Nc1nccs1)c2ccc(N)cc2
InChI InChI=1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12) checkYKey:JNMRHUJNCSQMMB-UHFFFAOYSA-N checkY
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Sulfathiazole is an organosulfur compound used as a short-acting sulfa drug.[1] Formerly, it was a common oral and topical antimicrobial, until less toxic alternatives were discovered.[2]

Sulfathiazole exists in various forms (polymorphs). The imine tautomer is dominant in solid samples.[3]

Cultural references

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  1. ^ Mertschenk B, Beck F, Bauer W (2002). "Thiourea and Thiourea Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Wiley-VCH. doi:10.1002/14356007.a26_803. ISBN 3527306730.
  2. ^ Rouf A, Tanyeli C (June 2015). "Bioactive thiazole and benzothiazole derivatives". European Journal of Medicinal Chemistry. 97: 911–27. doi:10.1016/j.ejmech.2014.10.058. PMID 25455640.
  3. ^ Kruger GT, Gafner G (February 1971). "The crystal structure of sulphathiazole II". Acta Crystallographica Section B. 27 (2): 326–33. Bibcode:1971AcCrB..27..326K. doi:10.1107/S0567740871002176.
  4. ^ Chapman FS (1949). The Jungle is Neutral. WW norton. p. 108.