CAS 692-29-5
:4-Oxobutanoic acid
Description:
4-Oxobutanoic acid, also known as 4-oxobutanoate or 4-ketopentanoic acid, is a five-carbon dicarboxylic acid characterized by the presence of a ketone functional group at the fourth carbon position. Its molecular formula is C5H8O3, and it features both a carboxylic acid group and a ketone, which contribute to its reactivity and potential applications in organic synthesis. This compound is typically a colorless to pale yellow liquid or solid, depending on its state and purity. It is soluble in water and polar organic solvents, making it versatile for various chemical reactions. 4-Oxobutanoic acid can participate in condensation reactions, serving as a building block in the synthesis of more complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it may exhibit biological activity, which can be of interest in medicinal chemistry. Proper handling and storage are essential, as with many organic acids, to ensure safety and stability.
Formula:C4H6O3
InChI:InChI=1S/C4H6O3/c5-3-1-2-4(6)7/h3H,1-2H2,(H,6,7)
InChI key:InChIKey=UIUJIQZEACWQSV-UHFFFAOYSA-N
SMILES:C(C(O)=O)CC=O
Synonyms:- 3-Formylpropanoic acid
- 3-Formylpropionic acid
- 4-Oxobutyric Acid
- Butanoic Acid, 4-Oxo-
- Butyraldehydic acid
- Propanoic acid, 3-formyl-
- Succinaldehydic acid
- Succinic acid semialdehyde
- Succinic semialdehyde
- β-Formylpropionic acid
- γ-Oxybutyric acid
- See more synonyms
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Found 4 products.
β-Formylpropionic Acid
CAS:Controlled Product<p>Applications β-Formylpropionic Acid is used in the synthesis of potent and orally available nonpeptide antagonist of human gonadotropin-releasing hormone receptor. It is also a reagent in the synthesis of human melanocortin-4 receptor antagonists with a pyrrolidinone moiety.<br>References Chen, C. et al.: J. Med. Chem., 51, 7478 (2008); Jiang, W. et al.: Bioorg. Med. Med. Chem. Lett., 17, 5610 (2007);<br></p>Formula:C4H6O3Color and Shape:NeatMolecular weight:102.09Succinicsemialdehyde
CAS:<p>Succinicsemialdehyde is a semialdehyde that is formed by the oxidative degradation of succinic acid. Succinicsemialdehyde has been shown to have high affinity for 5-HT3 receptors, which are found in the gastrointestinal tract and are involved in intestinal motility and bowel disease. The 5-HT3 receptor has been shown to be an important target for the treatment of irritable bowel syndrome. This semialdehyde also inhibits polymerase chain reaction (PCR) activity, which may be due to its ability to inhibit DNA synthesis. Succinicsemialdehyde has been shown to inhibit enzymes involved in energy metabolism, such as glutamate dehydrogenase and pyruvate formate lyase. The structural analysis of this molecule shows a keto group at C2, which indicates that it is a keto acid.</p>Formula:C4H6O3Purity:Min. 95%Color and Shape:PowderMolecular weight:102.09 g/mol



