Z-Lys(Boc)-ONp

Z-Lys(Boc)-ONp contains a lysine α-amino acid framework bearing an Nα-protecting benzyloxycarbonyl (Z) group and a Boc-protected side-chain amino (Lys(Boc)), with the carboxyl functionality converted to an ONp ester (ONp = p-nitrophenyl ester). The molecule therefore presents a protected α-amino acid moiety, a Boc-protected ε-amino group, and an activated carboxyl ester that can undergo nucleophilic acyl substitution under appropriate conditions while the Z and Boc groups help control chemoselectivity by masking the amines. Z-Lys(Boc)-ONp is used as a protected, activated amino acid derivative and acylating intermediate in peptide synthesis workflows and in solution-phase or solid-phase assembly strategies where stepwise coupling of the protected lysine residue is required.

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

CAT No: CP26815

CAS No:2212-69-3

Synonyms/Alias:Z-Lys(Boc)-ONp;2212-69-3;(S)-4-Nitrophenyl2-(((benzyloxy)carbonyl)amino)-6-((tert-butoxycarbonyl)amino)hexanoate;SCHEMBL7302025;CTK8E9760;MolPort-003-939-914;1216AB;ZINC71788211;AKOS015841480;AKOS016002115;AK-49576;AB0089596;KB-118005;TC-066815;ST24036192;Z-N-Epsilon-boc-L-lysine4-nitrophenylester;J-300185;Q-101588

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M.F/Formula
C25H31N3O8
M.W/Mr.
501.54
Size
5 g;25 g;
InChI
1S/C25H31N3O8/c1-25(2,3)36-23(30)26-16-8-7-11-21(27-24(31)34-17-18-9-5-4-6-10-18)22(29)35-20-14-12-19(13-15-20)28(32)33/h4-6,9-10,12-15,21H,7-8,11,16-17H2,1-3H3,(H,26,30)(H,27,31)/t21-/m0/s1
InChI Key
XBMRVOHLFIZDDV-NRFANRHFSA-N
Canonical SMILES
CC(C)(C)OC(=O)NCCCCC(C(=O)OC1=CC=C(C=C1)[N+](=O)[O-])NC(=O)OCC2=CC=CC=C2

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