Z-Lys(Boc)-OH · DCHA

Z-Lys(Boc)-OH · DCHA is a protected lysine derivative in which the α-amino group is carbobenzyloxy (Z/Cbz) protected, the ε-amino side chain is Boc-protected, and the carboxyl group is present as a free acid, forming a salt with dicyclohexylamine (DCHA). The molecule contains two protected amine functionalities that control chemoselectivity during stepwise peptide assembly, while the Boc and Z groups provide orthogonal deprotection behavior relative to unprotected amino acid functionality. As a protected amino acid salt, it is used as a building block for peptide synthesis workflows and for preparing lysine-containing peptide intermediates where controlled handling of the ε-amino group is required.

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

CAT No: CP26816

CAS No:2212-76-2

Synonyms/Alias:2212-76-2;Dicyclohexylamine(S)-2-(((benzyloxy)carbonyl)amino)-6-((tert-butoxycarbonyl)amino)hexanoate;Z-LYS(BOC)-OHDCHA;Z-Lys(Boc)-OHdicyclohexylaminesalt;N-Cbz-N'-Boc-L-lysinedicyclohexylamine;Z-Lys(Boc)-OH(dicyclohexylammonium)salt;N-epsilon-butoxycarbonyl-N-alpha-Z-L-lysinedchasalt;EINECS218-663-1;Z-Lys(Boc)-OHCHA;15550_ALDRICH;AC1O538R;SCHEMBL4750337;15550_FLUKA;CTK1A5820;MolPort-003-926-853;C31H51N3O6;ANW-61101;CZ-040;AKOS015840976;AKOS015892644;Z-Lys(Boc)-OHdicyclohexylammoniumsalt;AK-61245;AN-50546;OR008863;TC-066813

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M.F/Formula
C31H51N3O6
M.W/Mr.
561.76
Size
5 g;25 g;100 g;
InChI
1S/C19H28N2O6.C12H23N/c1-19(2,3)27-17(24)20-12-8-7-11-15(16(22)23)21-18(25)26-13-14-9-5-4-6-10-14;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h4-6,9-10,15H,7-8,11-13H2,1-3H3,(H,20,24)(H,21,25)(H,22,23);11-13H,1-10H2/t15-;/m0./s1
InChI Key
VTDLJMATIHSOTR-RSAXXLAASA-N
Canonical SMILES
CC(C)(C)OC(=O)NCCCCC(C(=O)O)NC(=O)OCC1=CC=CC=C1.C1CCC(CC1)NC2CCCCC2

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