1060769-55-2 | (S)-Fmoc-2-amino-5-[(N'-Pbf-N''-tert-butoxy)-guanidino]-pentanoic acid

Packsize	Purity	Availability	Price	Discounted Price
25mg	98%	in stock	$399.00	$279.00
100mg	98%	in stock	$800.00	$560.00
250mg	98%	in stock	$1,509.00	$1,056.00
1g	98%	in stock	$3,126.00	$2,188.00

Description

• Catalog Number: AE16003
• Chemical Name: (S)-Fmoc-2-amino-5-[(N'-Pbf-N''-tert-butoxy)-guanidino]-pentanoic acid
• CAS Number: 1060769-55-2
• Molecular Formula: C38H48N4O8S
• Molecular Weight: 720.8747
• MDL Number: MFCD18782824
• SMILES: O=C(N[C@H](C(=O)O)CCC/N=C(NS(=O)(=O)c1c(C)c(C)c2c(c1C)CC(O2)(C)C)/NOC(C)(C)C)OCC1c2ccccc2-c2c1cccc2

Upstream Synthesis Route

The (S)-Fmoc-2-amino-5-[(N'-Pbf-N''-tert-butoxy)-guanidino]-pentanoic acid is a versatile compound widely utilized in chemical synthesis due to its unique properties and functionality. It serves as a key building block in peptide synthesis, particularly in the solid-phase peptide synthesis (SPPS) method. This compound plays a crucial role in protecting and activating amino groups during the assembly of peptide chains, allowing for controlled and efficient elongation of the desired peptide sequence.Moreover, (S)-Fmoc-2-amino-5-[(N'-Pbf-N''-tert-butoxy)-guanidino]-pentanoic acid is commonly employed in the modification and derivatization of peptides, enabling the introduction of specific functional groups or labels for various research and therapeutic applications. Its guanidino group confers unique reactivity and selectivity, making it a valuable tool for chemists in designing and synthesizing complex peptide structures with precise control over the chemical modifications.In addition to peptide chemistry, this compound finds utility in medicinal chemistry, combinatorial chemistry, and bioconjugation strategies, where precise and high-yielding synthesis of peptide conjugates is essential for drug discovery, biomaterials development, and biochemical research. Its compatibility with standard peptide coupling protocols further enhances its versatility and applicability in diverse synthetic pathways, making it a sought-after reagent in modern chemical synthesis endeavors.