N-ε-2-chloro-Z-D-lysine

N-ε-2-chloro-Z-D-lysine is a protected, non-natural lysine derivative in which the ε-amino group is acylated with a Z-type protecting group and the side chain bears a 2-chloro substituent on the terminal carbon. The molecule contains a free α-amino and α-carboxyl functional group alongside a chlorinated ε-side-chain handle, with the D stereochemical designation specified for the lysine backbone. In peptide and amino acid synthesis, the Z-protected ε-amino functionality supports chemoselective stepwise coupling while the 2-chloro substituent provides a reactive site for further derivatization or for incorporation into structure-activity and chemical labeling workflows.

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

CAT No: CP01465

CAS No:201014-19-9

Synonyms/Alias:H-D-LYS(2-CL-Z)-OH;Nepsilon-2-Chloro-Z-D-lysine;201014-19-9;SCHEMBL3925964;CTK8F0219;MolPort-020-003-829;ZINC2556570;RT-014685;V4160;K-5875

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M.F/Formula
C14H19ClN2O4
M.W/Mr.
314.7
Abbr
H-D-Lys(2-Cl-Z)-OH
InChI
1S/C14H19ClN2O4/c15-11-6-2-1-5-10(11)9-21-14(20)17-8-4-3-7-12(16)13(18)19/h1-2,5-6,12H,3-4,7-9,16H2,(H,17,20)(H,18,19)/t12-/m1/s1
InChI Key
YCQVFPIEKSYHFI-GFCCVEGCSA-N
Canonical SMILES
C1=CC=C(C(=C1)COC(=O)NCCCCC(C(=O)O)N)Cl

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