Atomfair Pyrrolidine-2,4-dicarboxylic acid Pdc-2,4 C6H9NO4

Description Pyrrolidine-2,4-dicarboxylic acid (CAS No. 6320-02-1) is a high-purity, organic compound with the molecular formula C6H9NO4. This dicarboxylic acid derivative of pyrrolidine is a valuable building block in pharmaceutical and biochemical research, particularly in the synthesis of peptidomimetics and enzyme inhibitors. Its rigid pyrrolidine backbone and dual carboxylic acid functionalities make it an ideal scaffold for designing bioactive molecules. Available in >98% purity (HPLC), this compound is supplied as a white to off-white crystalline powder, ensuring consistency for sensitive applications. Store under inert conditions at 2-8??C to maintain stability. Suitable for use in: Medicinal chemistry research Peptide modification studies Enzyme…

Description

Pyrrolidine-2,4-dicarboxylic acid (CAS No. 6320-02-1) is a high-purity, organic compound with the molecular formula C₆H₉NO₄. This dicarboxylic acid derivative of pyrrolidine is a valuable building block in pharmaceutical and biochemical research, particularly in the synthesis of peptidomimetics and enzyme inhibitors. Its rigid pyrrolidine backbone and dual carboxylic acid functionalities make it an ideal scaffold for designing bioactive molecules. Available in >98% purity (HPLC), this compound is supplied as a white to off-white crystalline powder, ensuring consistency for sensitive applications. Store under inert conditions at 2-8??C to maintain stability. Suitable for use in:

Medicinal chemistry research
Peptide modification studies
Enzyme inhibitor development
Chiral synthesis applications

CAS No: 6320-02-1
Molecular Formula: C6H9NO4
Molecular Weight: 159.14
Exact Mass: 159.05315777
Monoisotopic Mass: 159.05315777
IUPAC Name: pyrrolidine-2,4-dicarboxylic acid
SMILES: C1C(CNC1C(=O)O)C(=O)O
Synonyms: Pyrrolidine-2,4-dicarboxylic acid, 99319-03-6, 2,4-Pyrrolidinedicarboxylic acid, Pdc-2,4, Pyrrolidine-2,4-dicarboxylate

Application

Pyrrolidine-2,4-dicarboxylic acid serves as a versatile intermediate in pharmaceutical research, particularly for developing constrained peptide analogs due to its rigid pyrrolidine structure. The compound’s dual carboxyl groups enable facile conjugation chemistry for creating novel enzyme inhibitors targeting metalloproteases and other carboxylate-recognizing enzymes. Researchers utilize this scaffold in structure-activity relationship studies to explore bioactive conformations of peptide-based therapeutics.

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