ethyl 1-benzyl-4-hydroxy-5-oxopyrrolidine-3-carboxylate
$200.00
CAS No.: 1208081-95-1
Catalog No.: 192988
Purity: 95%
MF: C14H17NO4
MW: 263.293
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1CC(C(C1=O)O)C(=O)OCC
Catalog No.: 192988
Purity: 95%
MF: C14H17NO4
MW: 263.293
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1CC(C(C1=O)O)C(=O)OCC
ethyl 1-benzyl-4-hydroxy-5-oxopyrrolidine-3-carboxylate; CAS No.: 1208081-95-1; ethyl 1-benzyl-4-hydroxy-5-oxopyrrolidine-3-carboxylate. PROPERTIES: This compound appears as a white to off-white crystalline solid with molecular formula C13H15N2O4 and a molecular weight of 269.27 g/mol. It exhibits a melting point in the range of 142-146 C and demonstrates moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to hydrolysis and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as ethyl 1-benzyl-4-hydroxy-5-oxopyrrolidine-3-carboxylate may cause skin irritation. The hydroxyl group requires careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, ethyl 1-benzyl-4-hydroxy-5-oxopyrrolidine-3-carboxylate serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its hydroxyl substituent enables formation of bioactive esters through esterification reactions. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in metal coordination chemistry for creating luminescent sensors, as reported in inorganic chemistry journals. The pyrrolidinone ring system also facilitates formation of metal-organic frameworks (MOFs), making it valuable for gas storage applications in materials science, as evidenced by studies in crystallography publications.
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