Fenamic acid
From Self-sufficiency
| Fenamic acid | |
|---|---|
| File:Fenamic acid.png | |
| 2-(phenylamino)benzoic acid | |
| Other names N-phenylanthranilic acid | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 91-40-7 |
| PubChem | 4386 |
| SMILES | Script error: No such module "collapsible list". |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C13H11NO2 |
| Molar mass | 213.23 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Fenamic acid is a molecule which serves as a parent structure for several non-steroidal anti-inflammatory drugs, including mefenamic acid, tolfenamic acid, flufenamic acid, and meclofenamic acid.
This compound may be synthesized by the reaction of 2-chlorobenzoic acid and aniline, with base and copper oxide catalyst in the Goldberg reaction.[1]
The self-condensation of fenamic acid yields acridone.[1]
References
- ↑ 1.0 1.1 C. F. H. Allen and G. H. W. McKee (1943), "Acridone", Org. Synth.; Coll. Vol., 2: 15 Missing or empty
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