N-α-Z-N-ε-Boc-D-lysine

N-α-Z-N-ε-Boc-D-lysine is a protected lysine derivative in which the α-amino group is carbobenzyloxy (Z/Cbz) protected and the ε-amino group is tert-butoxycarbonyl (Boc) protected, while the side chain retains the characteristic (CH2)4 amine-bearing lysine skeleton. The molecule contains a free carboxylic acid functional group and a D-stereochemical configuration at the α-carbon as indicated by the product name, with two orthogonally protected amino functionalities that can be unmasked selectively under appropriate deprotection conditions. It is employed as a stepwise building block for peptide synthesis and related amide bond formation, enabling controlled incorporation of lysine residues with orthogonally removable protecting groups for sequential coupling and chemoselective derivatization.

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

CAT No: CP01455

CAS No:66845-42-9

Synonyms/Alias:Z-D-Lys(Boc)-OH;66845-42-9;Z-Lys(Boc)-OH;CBZ-D-LYS(BOC)-OH;Nalpha-Z-Nepsilon-Boc-D-lysine;Nalpha-Cbz-Nepsilon-Boc-D-Lysine;N-Benzyloxycarbonyl-N'-(tert-Butoxycarbonyl)-L-lysine;AmbotzZAA1151;PubChem12957;AC1OJJ8V;N|A-Z-N|A-Boc-D-lysine;96019_ALDRICH;N|A-Cbz-N|A-Boc-D-Lysine;Cbz-D-Lys(Boc)-OH.DCHA;SCHEMBL2467817;96019_FLUKA;MolPort-003-939-913;ACT03124;ZINC4521932;CZ-075;AKOS015841476;AJ-51476;AK-46019;BR-46019;SC-09719

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M.F/Formula
C19H28N2O6
M.W/Mr.
380.4
Abbr
Z-D-Lys(Boc)-OH
InChI
1S/C19H28N2O6/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/h4-6,9-10,15H,7-8,11-13H2,1-3H3,(H,20,24)(H,21,25)(H,22,23)/t15-/m1/s1
InChI Key
DYSBKEOCHROEGX-OAHLLOKOSA-N
Canonical SMILES
CC(C)(C)OC(=O)NCCCCC(C(=O)O)NC(=O)OCC1=CC=CC=C1

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