Fenamic acid

Names
Preferred IUPAC name 2-Anilinobenzoic acid
Other names N-phenylanthranilic acid
Identifiers
CAS Number	91-40-7 Y
3D model ( JSmol)	Interactive image
ChEBI	CHEBI:34756 N
ChEMBL	ChEMBL23832 N
ChemSpider	4233 N
ECHA InfoCard	100.001.879
IUPHAR/BPS	4182
PubChem CID	4386
UNII	952VN06WBB Y
CompTox Dashboard ( EPA)	DTXSID6059025
InChI InChI=1S/C13H11NO2/c15-13(16)11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9,14H,(H,15,16) N Key: ZWJINEZUASEZBH-UHFFFAOYSA-N N InChI=1/C13H11NO2/c15-13(16)11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9,14H,(H,15,16) Key: ZWJINEZUASEZBH-UHFFFAOYAQ
SMILES C1=CC=C(C=C1)NC2=CC=CC=C2C(=O)O
Properties
Chemical formula	C13H11NO2
Molar mass	213.23 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N  verify ( what is YN ?) Infobox references

Fenamic acid is an organic compound, which, especially in its ester form, is called fenamate. ^[1]: 458 serves as a parent structure for several nonsteroidal anti-inflammatory drugs (NSAIDs), including mefenamic acid, tolfenamic acid, flufenamic acid, and meclofenamic acid. These drugs are commonly referred to as "anthranilic acid derivatives" or "fenamates" because fenamic acid is a derivative of anthranilic acid. ^{[2]: 235  [3]: 17  [2]}

Fenamic acid can be synthesized from 2-chlorobenzoic acid and can be converted into acridone. ^[4]

References