2-Oxopent-4-enoic acid
Appearance
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Names | |
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Preferred IUPAC name
2-Oxopent-4-enoic acid | |
Other names
2-Keto-4-pentenoic acid
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Identifiers | |
3D model (JSmol)
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1851398 | |
ChEBI | |
ChemSpider | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C5H6O3 | |
Molar mass | 114.100 g·mol−1 |
Related compounds | |
Related compounds
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Pentenoic acid; 4-Hydroxy-3-pentenoic acid; 2-Amino-5-chloro-4-pentenoic acid; (2R)-2-Methylpent-4-enoic acid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2-Oxopent-4-enoic acid (2-oxopent-4-enoate) is formed by the dehydration of 4-hydroxy-2-oxopentanoate by 2-oxopent-4-enoate hydratase or by the hydrolysis of 2-hydroxymuconate semialdehyde by 2-hydroxymuconate-semialdehyde hydrolase.[1]
References
[edit]- ^ Sala-Trepat JM, Evans WC (1971). "The meta cleavage of catechol by Azotobacter species 4-Oxalocrotonate pathway". Eur. J. Biochem. 20 (3): 400–13. doi:10.1111/j.1432-1033.1971.tb01406.x. PMID 4325686.
External links
[edit]- Oxopentenoate, biocyc.org