CAS 1821-02-9
:2-Oxovaleric acid
Description:
2-Oxovaleric acid, also known as 4-oxopentanoic acid, is a five-carbon dicarboxylic acid characterized by the presence of a ketone functional group adjacent to a carboxylic acid group. Its molecular formula is C5H8O3, and it features a carbonyl group (C=O) at the second carbon position, which contributes to its reactivity and potential applications in organic synthesis. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in water and organic solvents, making it versatile for various chemical reactions. 2-Oxovaleric acid can participate in condensation reactions, serving as a precursor for the synthesis of more complex molecules, including pharmaceuticals and agrochemicals. Additionally, it may play a role in metabolic pathways, particularly in the degradation of certain amino acids. Safety data indicates that it should be handled with care, as it may cause irritation upon contact with skin or eyes. Overall, 2-oxovaleric acid is an important compound in both industrial and biochemical contexts.
Formula:C5H8O3
InChI:InChI=1S/C5H8O3/c1-2-3-4(6)5(7)8/h2-3H2,1H3,(H,7,8)
InChI key:InChIKey=KDVFRMMRZOCFLS-UHFFFAOYSA-N
SMILES:C(CCC)(C(O)=O)=O
Synonyms:- 2-Keto-n-valeric acid
- 2-Ketopentanoate
- 2-Ketopentanoic acid
- 2-Ketovaleric acid
- 2-Oxo-n-valeric acid
- 2-Oxopentanoic acid
- A-ketovaleric acid free acid
- Ketovalericacid
- Pentanoic acid, 2-oxo-
- Valeric acid, 2-oxo-
- α-Ketovaleric acid
- α-Oxo-n-valeric acid
- α-Oxopentanoic acid
- α-Oxovaleric acid
- See more synonyms
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Found 6 products.
2-Oxovaleric acid
CAS:<p>2-Oxovaleric acid (2-Oxopentanoic acid) is a potential biomarker for identifying aortic valve stenosis (AVS).</p>Formula:C5H8O3Color and Shape:LiquidMolecular weight:116.122-Oxovaleric Acid
CAS:Formula:C5H8O3Purity:>95.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:116.122-Oxovaleric acid
CAS:<p>2-Oxovaleric acid is a monocarboxylic acid that is produced by the oxidation of 2-oxopentanoic acid. It was first discovered as an inhibitory compound for glutamate dehydrogenase, which catalyzes the conversion of glutamate to alpha-ketoglutarate. This inhibition leads to a buildup of glutamate in the cell, which can cause metabolic disorders. The importance of 2-oxovaleric acid was demonstrated using a chromatographic method on type strain cells. The electron microscopic images showed that 2-oxovaleric acid inhibited the growth of bacteria by binding to extracellular Ca2+, carbon source, and animals.</p>Formula:C5H8O3Purity:Min. 95%Molecular weight:116.12 g/mol




