106982-77-8 | (S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-5-oxopyrrolidine-2-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$60.00	$42.00
250mg	97%	in stock	$137.00	$96.00
1g	97%	in stock	$328.00	$230.00
5g	97%	in stock	$1,007.00	$705.00
10g	97%	in stock	$1,535.00	$1,074.00

Description

• Catalog Number: AE51881
• Chemical Name: (S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-5-oxopyrrolidine-2-carboxylic acid
• CAS Number: 106982-77-8
• Molecular Formula: C20H17NO5
• Molecular Weight: 351.35268
• MDL Number: MFCD27952004
• SMILES: OC(=O)[C@@H]1CCC(=O)N1C(=O)OCC1c2ccccc2-c2c1cccc2

Upstream Synthesis Route

FMoc-5-oxo-L-proline, also known as 5-oxo-L-proline with a 9-fluorenylmethyloxycarbonyl (FMoc) protecting group, is a valuable building block in chemical synthesis. This compound is commonly utilized in peptide chemistry and organic synthesis due to its versatility and compatibility with standard peptide coupling procedures.In peptide synthesis, FMoc-5-oxo-L-proline serves as a key intermediate for the preparation of peptide analogs and modified amino acids. The FMoc protecting group allows for selective deprotection under mild conditions, facilitating the synthesis of complex peptides with high purity. Additionally, the presence of the 5-oxo group provides unique reactivity, enabling further functionalization and diversification of peptide structures.Furthermore, FMoc-5-oxo-L-proline can be employed in the synthesis of peptidomimetics, drug conjugates, and bioconjugates with tailored pharmacological properties. Its strategic incorporation into peptide sequences can modulate biological activity, enhance stability, and improve pharmacokinetic profiles of peptide-based therapeutics.Overall, the application of FMoc-5-oxo-L-proline in chemical synthesis offers a powerful tool for the efficient and precise assembly of peptide molecules with customized functionality and bioactivity.