Fenamic acid: Difference between revisions
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Revision as of 08:15, 26 February 2010
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Names | |
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IUPAC name
2-(phenylamino)benzoic acid
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Other names
N-phenylanthranilic acid
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Identifiers | |
3D model (JSmol)
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ECHA InfoCard | 100.001.879 |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
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).
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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
- ^ a b C. F. H. Allen and G. H. W. McKee (1943). "Acridone". Organic Syntheses; Collected Volumes, vol. 2, p. 15.