Z-L-Aha-OH*DCHA is a protected, amino acid derivative featuring an L-configured amino acid backbone bearing a Z (benzyloxycarbonyl/Cbz-type) carbamate protecting group and a carboxylic acid functionality, with the side chain corresponding to Aha (aminohexanoic acid) and the molecule presented as a DCHA salt complex. The structure contains an N-protecting carbamate that masks the amino group to control chemoselectivity during coupling, while the free carboxylic acid and the protonated salt form with DCHA provide defined handling characteristics for solid-phase or solution-phase peptide assembly. Z-L-Aha-OH*DCHA is used as a stepwise building block for the preparation of peptides and peptide-related intermediates where controlled incorporation of the Aha residue and protection of the amino functionality are required for sequential synthesis and downstream deprotection strategies.
CAT No: CP25275
CAS No:1263047-43-3
Synonyms/Alias:Z-L-AHA-OHDCHA;7927AH;KM5487;C12H23N.C12H14N4O4;1263047-43-3
Chemical Name:Z-L-Dab(N3)-OH, N-alpha-Benzyloxycarbonyl-4-azido-L-homoalanine, (S)-2-Benzyloxycarbonylamino-4-azidobutanoic acid dicyclohexylamine
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