Fmoc-L-Cyclopentylalanine is a synthetic amino acid derivative characterized by the presence of a cyclopentyl group attached to the alpha carbon of the alanine structure. The "Fmoc" (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, commonly used in peptide synthesis to prevent unwanted reactions during the coupling process. This compound is typically utilized in the field of organic chemistry and peptide synthesis due to its unique side chain, which can impart specific steric and electronic properties to peptides. The cyclopentyl group can enhance the hydrophobic character of the amino acid, potentially influencing the folding and stability of peptides in aqueous environments. Fmoc-L-Cyclopentylalanine is often employed in the development of novel peptides for research purposes, including studies on protein structure and function, as well as in drug design. Its CAS number, 371770-32-0, allows for easy identification and procurement in chemical databases and suppliers.

Fmoc-L-CyClopentylalanine

371770-32-0: Fmoc-Cpa-OH,  (9H-Fluoren-9-yl)MethOxy]Carbonyl β-Cyclopentyl-L-Alanine,  FMOC-L-CYCPENTALA-OH,  N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-2-CYCLOPENTYL-L-ALANINE,  FMoc-(S)-3-Cyclopentylalanine,  FMOC-ALA(CPEN)-OH

FMOC-L-CYCPENTALA-OH

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CAS 371770-32-0: Fmoc-L-CyClopentylalanine

FMOC-L-CYCPENTALA-OH

Ref: IN-DA00C7ZR

Fmoc-Cpa-OH

Ref: 3D-WPA77032

Fmoc-(S)-3-Cyclopentylalanine

Ref: 54-OR919154

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-cyclopentylpropanoic acid

Ref: 10-F337558