N-ε-2-chloro-Z-L-lysine is a Z-protected, L-lysine-derived amino acid derivative in which the ε-amino group is functionalized with a 2-chloro substituent, yielding a lysine side chain bearing a chloro handle. The molecule contains an α-amino group and a carboxyl group consistent with an amino acid scaffold, while the N-ε position is modified and the Z (benzyloxycarbonyl-type) protection on the amino functionality controls chemoselectivity by suppressing undesired amine reactivity during peptide-related transformations. In synthesis and chemical biology workflows, the chlorinated ε-substituent provides a site for further derivatization or incorporation into protected lysine building blocks for preparing substituted amino acid and peptide analogues.
CAT No: CP01466
CAS No:42390-97-6
Synonyms/Alias:H-Lys(2-Cl-Z)-OH;42390-97-6;AC1MBOX6;SCHEMBL4413196;MolPort-002-915-555;RJC01689;ZINC2556571;CCG-47813;AKOS025289381;MCULE-4635419929;AK170099;X3377;K-8807;L-Lysine,N6-[[(2-chlorophenyl)methoxy]carbonyl]-;SR-01000637406-1;(2S)-2-amino-6-[(2-chlorophenyl)methoxycarbonylamino]hexanoicacid
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