Boc-Lys(2-Cl-Z)-OH TCI B6148

Chemical Identity

Other names: Boc-Lys(2-Cl-Z)-OH · N2-(tert-Butoxycarbonyl)-N6-[[(2-chlorobenzyl)oxy]carbonyl]-L-lysine · Nalpha-(tert-Butoxycarbonyl)-Nepsilon-(2-chlorocarbobenzoxy)-L-lysine · Boc-Lys(2-Cl-Cbz)-OH · Nalpha-Boc-Nepsilon-(2-chloro-Cbz)-L-
CAS No.: 54613-99-9
PubChem: CID 7269331·SID 468590940
Formula: C19H27ClN2O6
Molecular weight: 414.88 g/mol
Purity: >98.0%(T)
Storage: 0-10°C
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-6-[(2-chlorophenyl)methoxycarbonylamino]-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
SMILES: CC(C)(C)OC(=O)NC(CCCCNC(=O)OCC1=CC=CC=C1Cl)C(=O)O
InChIKey: ATUMDPHEFWGCJF-HNNXBMFYSA-N
MDL: MDL00038386

Rp 900.900,00

~~Rp 645.750,00~~ Rp 900.900,00

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Berat 5g 25g

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Boc-Lys(2-Cl-Z)-OH is a doubly protected lysine derivative widely employed as a building block in solid-phase peptide synthesis (SPPS). The Boc group protects the α-amino terminus while the 2-Cl-Z group safeguards the ε-amino side chain, enabling selective orthogonal deprotection during peptide chain elongation. This high-purity TCI reagent is suitable for the synthesis of branched peptides, cyclic peptides, and peptide conjugates in pharmaceutical and biochemical research settings.