Z-L-Dap(N3)-OH*CHA is a protected, modified amino acid derivative featuring an azido-functionalized side chain on a diaminopropyl framework, where "Z" denotes a benzyloxycarbonyl (Cbz/Z) protecting group on the amino functionality and the "N3" indicates a terminal azide substituent. The molecule bears both an amino-protecting carbamate and a free carboxylic acid (-COOH), and the "L-Dap" designation specifies the stereochemical form relative to L-2,3-diaminopropionic acid while the appended "*CHA" indicates an additional structural association that can be relevant to handling or solid-state/solvation form. In peptide chemistry and chemical biology, the azide side chain provides a chemical handle for bioorthogonal conjugation or labeling workflows, while the Cbz-protected amino group supports controlled chemoselectivity during stepwise synthesis of azide-bearing peptide or amino acid building blocks.
CAT No: CP25989
CAS No:684270-44-8
Synonyms/Alias:Z-L-Aza-OH*CHA;Z-Aza-OH*CHA;Cbz-L-Aza-OH*CHA;Cbz-Aza-OH*CHA;Z-L-beta-azidoalanine cyclohexylamine salt;N-alpha-Benzyloxycarbonyl-3-azido-L-alanine cyclohexylamine salt
Chemical Name:(S)-2-Benzyloxycarbonylamino-3-azidopropanoic acid cyclohexylamine
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