1219424-59-5 | 1-Benzyl-3-n-cbz-amino-2,5-dioxo-pyrrolidine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$47.00	$33.00
5g	95%	in stock	$131.00	$92.00
10g	95%	in stock	$211.00	$148.00

Description

• Catalog Number: AA54792
• Chemical Name: 1-Benzyl-3-n-cbz-amino-2,5-dioxo-pyrrolidine
• CAS Number: 1219424-59-5
• Molecular Formula: C19H18N2O4
• Molecular Weight: 338.3572
• MDL Number: MFCD12965073
• SMILES: O=C(NC1CC(=O)N(C1=O)Cc1ccccc1)OCc1ccccc1

Upstream Synthesis Route

Benzyl (1-benzyl-2,5-dioxopyrrolidin-3-yl)carbamate, often referred to as Boc-L-proline, is a versatile compound widely utilized in chemical synthesis. Its unique chemical structure and reactivity make it a valuable building block in the preparation of various compounds and materials.In organic synthesis, Boc-L-proline is commonly employed as a protecting group for the carboxylic acid functionality present in amino acids or peptides. By selectively masking the carboxyl group with the Boc (tert-butoxycarbonyl) moiety, Boc-L-proline enables specific chemical transformations to be carried out without affecting other reactive sites within the molecule. This protection-deprotection strategy is crucial in the synthesis of complex peptides and natural products, where precise control over reaction pathways and regioselectivity is essential.Furthermore, Boc-L-proline serves as a key component in the preparation of chiral ligands, catalysts, and pharmaceutical intermediates. Its incorporation in the design of asymmetric catalysts allows for the enantioselective synthesis of various molecules, facilitating the production of optically pure compounds with high stereoselectivity. In pharmaceutical chemistry, Boc-L-proline derivatives have been utilized in the development of novel drug candidates and prodrug systems, exploiting their stability and reactivity profiles for targeted drug delivery and controlled release applications.Overall, the application of Benzyl (1-benzyl-2,5-dioxopyrrolidin-3-yl)carbamate in chemical synthesis encompasses a broad range of synthetic methodologies and strategic transformations, making it a fundamental and indispensable reagent in modern organic chemistry research and industrial processes.