cas: 61-68-7 — see every product listed under this CAS number, including other names
Mefenamic Acid (CAS 61-68-7) is a chemical reagent available from Chemat. Available pack sizes: on request, 250mg, 10mg, 10mM (in 1ml dmso), 50mg, 100g, 50g, 250g. Offered by: Chemat Brand, Mikromol, LoGiCal, Dr. Ehrenstorfer.
| brand | Chemat Brand |
|---|---|
| catalog number | ULM015 |
| cas | 61-68-7 |
| size | on request |
| availability | Do potwierdzenia przez Chemat|To be confirmed by Chemat |
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| brand | size | price | |
|---|---|---|---|
| Chemat Brand | on request | price on request | |
| Chemat Brand | on request | price on request | |
| Mikromol | 250mg | price on request | |
| LoGiCal | 10mg | price on request | |
| Dr. Ehrenstorfer | 250mg | price on request | |
| GLPBio | 10mM (in 1ml dmso) | 578.32 Pln | |
| GLPBio | 50mg | 648.53 Pln | |
| Biosynth | 100g | price on request | |
| Biosynth | 50g | price on request | |
| Biosynth | 250g | price on request | |
| Sigma-Aldrich | 250MG | 291.00 Pln | |
| HPC Standards | 1x250mg | 311.15 Pln |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Mefenamic acid is an aminobenzoic acid that is anthranilic acid in which one of the hydrogens attached to the nitrogen is replaced by a 2,3-dimethylphenyl group. Although classed as a non-steroidal anti-inflammatory drug, its anti-inflammatory properties are considered to be minor. It is used to relieve mild to moderate pain, including headaches, dental pain, osteoarthritis and rheumatoid arthritis. It has a role as a non-steroidal anti-inflammatory drug, an analgesic, an antipyretic, an EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor, a xenobiotic, an antirheumatic drug and an environmental contaminant. It is an aminobenzoic acid and a secondary amino compound.
Source: ChEBI
| Molecular formula | C15H15NO2 |
|---|---|
| Molecular weight | 241.28 g/mol |
| IUPAC name | 2-(2,3-dimethylanilino)benzoic acid |
| InChIKey | HYYBABOKPJLUIN-UHFFFAOYSA-N |
| SMILES | CC1=C(C(=CC=C1)NC2=CC=CC=C2C(=O)O)C |
Computed by PubChem (NCBI)