For research use only. Not for therapeutic Use.
Diflunisal is a salicylic acid derivative with analgesic and anti-inflammatory activity. It was developed by Merck Sharp & Dohme in 1971 after showing promise in a research project studying more potent chemical analogs of aspirin. It was first sold under the brand name Dolobid, marketed by Merck & Co., but generic versions are now widely available. It is classed as a non-steroidal anti-inflammatory drug (NSAID).
CAS Number | 22494-42-4 |
Synonyms | Dolobid, Dolobis, Flovacil, Fluniget |
Molecular Formula | C13H8F2O3 |
Purity | ≥95% |
Target | COX |
Solubility | Soluble in DMSO |
Storage | Store at -20°C |
IUPAC Name | 5-(2,4-difluorophenyl)-2-hydroxybenzoic acid |
InChI | InChI=1S/C13H8F2O3/c14-8-2-3-9(11(15)6-8)7-1-4-12(16)10(5-7)13(17)18/h1-6,16H,(H,17,18) |
InChIKey | HUPFGZXOMWLGNK-UHFFFAOYSA-N |
SMILES | C1=CC(=C(C=C1C2=C(C=C(C=C2)F)F)C(=O)O)O |
Reference | 1: Kaur A, Bhoop BS, Chhibber S, Sharma G, Gondil VS, Katare OP. Supramolecular <br> 3: Pandey P, Verma V, Gautam G, Kumari N, Dhar SK, Gourinath S. Targeting the 4: Pallipurath AR, Civati F, Sibik J, Crowley C, Zeitler JA, McArdle P, Erxleben 5: Azorín SE, Cabib CE, Campistol JM. Diflunisal compassive use in transthyretin 6: Tarushi A, Kakoulidou C, Raptopoulou CP, Psycharis V, Kessissoglou DP, Zoi I, 7: Kaur A, Goindi S, Katare OP. Formulation, characterisation and in vivo 8: Hendrix AS, Spoonmore TJ, Wilde AD, Putnam NE, Hammer ND, Snyder DJ, Guelcher 9: Perontsis S, Hatzidimitriou AG, Papadopoulos AN, Psomas G. Nickel-diflunisal 10: Shirakawa K, Wang L, Man N, Maksimoska J, Sorum AW, Lim HW, Lee IS, Shimazu |
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