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Z-L-Aha-OH*DCHA

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.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

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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M.F/Formula
C24H37N5O4
M.W/Mr.
278,26*181,34 g/mole
Size
1 g;5 g;
InChI
1S/C12H14N4O4.C12H23N/c13-16-14-7-6-10(11(17)18)15-12(19)20-8-9-4-2-1-3-5-9;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-5,10H,6-8H2,(H,15,19)(H,17,18);11-13H,1-10H2/t10-;/m0./s1
InChI Key
WWXXNIKKZNJTKM-PPHPATTJSA-N
Canonical SMILES
C1CCC(CC1)NC2CCCCC2.C1=CC=C(C=C1)COC(=O)NC(CCN=[N+]=[N-])C(=O)O

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