N-ε-Z-D-lysine is a protected lysine derivative in which the ε-amino group is carbamated with a benzyloxycarbonyl (Z, Cbz) protecting group, while the α-amino and α-carboxyl functionalities remain present as the free functional groups of the amino acid. The molecule is specified as the D stereochemical form of lysine, bearing a side-chain (-(CH2)4-) terminating in the Z-protected ε-nitrogen and thus presenting a controlled, masked primary amine for chemoselective transformations. In peptide and amino-acid derivative synthesis, N-ε-Z-D-lysine functions as a protected building block that supports stepwise assembly by limiting reactivity at the ε-position while the α-amino and carboxyl groups can be used for further coupling and elaboration.
CAT No: CP01470
CAS No:34404-32-5
Synonyms/Alias:34404-32-5;H-D-Lys(Z)-OH;N6-[(Phenylmethoxy)carbonyl]-R-lysine;(R)-2-Amino-6-(((benzyloxy)carbonyl)amino)hexanoicacid;D-Lys(Z)-OH;N-e-Z-D-lysine;AmbotzHAA6320;AC1LT505;SCHEMBL5816135;N6-(Benzyloxycarbonyl)-D-lysine;CKGCFBNYQJDIGS-GFCCVEGCSA-N;MolPort-003-940-657;ZINC1707768;AC-12926;AJ-30689;AK-49708;BC205413;ST2402616;K-7855;Q-101586;(2R)-2-amino-6-(phenylmethoxycarbonylamino)hexanoicacid;(2R)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoicacid;(2R)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoicacid
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