Loading AI tools
Chemical compound From Wikipedia, the free encyclopedia
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]
![]() | |
Names | |
---|---|
Preferred IUPAC name
2-Oxopent-4-enoic acid | |
Other names
2-Keto-4-pentenoic acid | |
Identifiers | |
3D model (JSmol) |
|
1851398 | |
ChEBI | |
ChemSpider | |
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C5H6O3 | |
Molar mass | 114.100 g·mol−1 |
Related compounds | |
Related compounds |
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).
|
Seamless Wikipedia browsing. On steroids.
Every time you click a link to Wikipedia, Wiktionary or Wikiquote in your browser's search results, it will show the modern Wikiwand interface.
Wikiwand extension is a five stars, simple, with minimum permission required to keep your browsing private, safe and transparent.