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Names | |
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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).
|
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).
|
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]