trans-1-benzyl 3-methyl 4-methoxypyrrolidine-1,3-dicarboxylate
$300.00
CAS No.: 2386461-85-2
Catalog No.: 193020
Purity: 95%
MF: C15H19NO5
MW: 293.319
Storage: 2-8 degree Celsius
SMILES: CO[C@H]1[C@@H](CN(C1)C(=O)OCC1=CC=CC=C1)C(=O)OC
Catalog No.: 193020
Purity: 95%
MF: C15H19NO5
MW: 293.319
Storage: 2-8 degree Celsius
SMILES: CO[C@H]1[C@@H](CN(C1)C(=O)OCC1=CC=CC=C1)C(=O)OC
trans-1-benzyl 3-methyl 4-methoxypyrrolidine-1,3-dicarboxylate; CAS No.: 2386461-85-2; trans-1-benzyl 3-methyl 4-methoxypyrrolidine-1,3-dicarboxylate. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C15H18NO6 and a molecular weight of 302.31 g/mol. It demonstrates a melting point in the range of 142-146 C and shows 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 trans-1-benzyl 3-methyl 4-methoxypyrrolidine-1,3-dicarboxylate may cause skin irritation. The ester groups require careful handling in strongly basic environments. APPLICATIONS: In medicinal chemistry, trans-1-benzyl 3-methyl 4-methoxypyrrolidine-1,3-dicarboxylate serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its methoxy substituent enables improved solubility in biological systems for enhanced bioavailability. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The pyrrolidine ring system also facilitates coordination with metal ions, making it valuable for creating coordination polymers in materials science applications, as evidenced by structural chemistry publications.
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