Nα, Nε-Bis-boc-L-lysine

• CAT Number: R005818
• CAS Number: 2483-46-7
• Molecular Formula: C16H30N2O6
• Molecular Weight: 346.424
• Purity: ≥95%
• Synonyms: Nα,Nε-Diboc-L-lysine; N2,N6-Bis[(1,1-dimethylethoxy)carbonyl]-L-lysine; (S)-2,6-Bis(tert-butoxycarbonylamino)hexanoic Acid; Di[N-(tert-butoxycarbonyl)]-L-lysine; NSC 164052
• Storage: -20°C
• IUPAC Name: (2S)-2,6-bis[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
• InChI: InChI=1S/C16H30N2O6/c1-15(2,3)23-13(21)17-10-8-7-9-11(12(19)20)18-14(22)24-16(4,5)6/h11H,7-10H2,1-6H3,(H,17,21)(H,18,22)(H,19,20)/t11-/m0/s1
• InChIKey: FBVSXKMMQOZUNU-NSHDSACASA-N
• SMILES: CC(C)(C)OC(=O)NCCCCC(C(=O)O)NC(=O)OC(C)(C)C

Nα, Nε-Bis-boc-L-lysine(CAT: R005818) is a compound used in organic synthesis and peptide chemistry. Its mode of action involves serving as a protected form of L-lysine, an essential amino acid. The compound contains two tert-butoxycarbonyl (Boc) protecting groups, one each on the α and ε amino groups of lysine. These protecting groups shield the amino groups from undesired reactions during peptide synthesis, allowing selective deprotection at a later stage. Nα, Nε-Bis-boc-L-lysine finds applications in peptide coupling, solid-phase peptide synthesis, and the construction of peptide-based drugs and bioactive molecules.