Urocanic acid
| Names | |
|---|---|
| Preferred IUPAC name
(2E)-3-(1H-imidazol-4-yl)prop-2-enoic acid | |
| Other names
(E)-3-(1H-imidazol-4-yl)acrylic acid | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.002.963 |
| MeSH | Urocanic+acid |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C6H6N2O2 | |
| Molar mass | 138.124 g/mol |
| Melting point | 225 °C (437 °F; 498 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Urocanic acid (formally trans-Urocanic acid) is an intermediate in the catabolism of L-histidine. The cis-urocanic acid isomer is rare.