2-Oxopyrrolidine-3-carboxylic acid, also known as proline-2-carboxylic acid, is a cyclic amino acid characterized by its five-membered ring structure containing both a carbonyl and a carboxylic acid functional group. This compound is notable for its role in various biochemical processes, particularly in protein synthesis and metabolism. It exhibits properties typical of amino acids, such as the ability to participate in hydrogen bonding due to its polar functional groups. The presence of the carbonyl group contributes to its reactivity, making it a potential intermediate in organic synthesis. Additionally, 2-oxopyrrolidine-3-carboxylic acid can exist in different tautomeric forms, influencing its chemical behavior. Its solubility in water and organic solvents varies, which can affect its applications in pharmaceuticals and biochemistry. Overall, this compound is of interest in both synthetic and biological chemistry due to its structural features and functional versatility.

2-oxopyrrolidine-3-carboxylic acid

96905-67-8: 3-Pyrrolidinecarboxylic Acid, 2-Oxo-

3-Pyrrolidinecarboxylic acid, 2-oxo-

2-Oxopyrrolidine-3-carboxylic acid is a carboxylic acid that has been shown to be an effective substrate for the oxidation of alcohols and racemates. The oxidative hydrolysis of 2-oxopyrrolidine-3-carboxylic acid yields lactones, which can then be used as starting materials for the synthesis of boronic esters. This molecule also has been shown to undergo aromatisation with phenylhydrazine and nitrogen atoms. 2-Oxopyrrolidine-3-carboxylic acid can be used in various reactions such as the synthesis of drugs and pharmaceuticals, pesticides, dyes, and intermediates for other chemicals.

CAS 96905-67-8: 2-oxopyrrolidine-3-carboxylic acid

3-Pyrrolidinecarboxylic acid, 2-oxo-

Ref: IN-DA00IJVH

2-Oxopyrrolidine-3-carboxylic acid

Ref: 3D-FO145104

2-Oxo-pyrrolidine-3-carboxylic acid

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