Z-L-Phe-OSu is a protected amino acid derivative consisting of L-phenylalanine bearing an N-benzyloxycarbonyl (Z, Cbz) protecting group and a reactive N-hydroxysuccinimide (OSu) ester at the carboxyl terminus. The molecule contains a carbamate-protected amino functionality and an activated ester that can undergo nucleophilic acyl substitution, while the phenyl side chain provides a hydrophobic aromatic group for residue-level structure-property studies. Z-L-Phe-OSu is used in peptide coupling and bioconjugation workflows as an activated amino acid building block that can form amide bonds with nucleophiles such as amines under standard acylation conditions.
CAT No: CP25775
CAS No:3397-32-8
Synonyms/Alias:Z-PHE-OSU;3397-32-8;C21H20N2O6;AmbotzZAA1237;SCHEMBL5689118;MolPort-006-115-310;7956AH;ZINC71788225;AKOS016369135;MCULE-6019819182;AK170092;KB-105428;FT-0698281;K-7793;N-(Benzyloxycarbonyl)-L-phenylalaninesuccinimidylester;N-Benzyloxycarbonylphenylalanine-N-hydroxysuccinimideester;L-Phenylalanine,N-[(phenylmethoxy)carbonyl]-,2,5-dioxo-1-pyrrolidinylester
Chemical Name:N-alpha-Benzyloxycarbonyl-L-phenylalanine succinimidyl ester
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