N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-((5-(dimethylamino)naphthalen-1-yl)sulfonyl)-L-lysine

• CAT Number: M028476
• CAS Number: 118584-90-0
• Molecular Formula: C33H35N3O6S
• Molecular Weight: 601.71
• Purity: ≥95%
• Synonyms: (2S)-6-[[5-(dimethylamino)naphthalen-1-yl]sulfonylamino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
• InChI: InChI=1S/C33H35N3O6S/c1-36(2)30-18-9-16-27-26(30)15-10-19-31(27)43(40,41)34-20-8-7-17-29(32(37)38)35-33(39)42-21-28-24-13-5-3-11-22(24)23-12-4-6-14-25(23)28/h3-6,9-16,18-19,28-29,34H,7-8,17,20-21H2,1-2H3,(H,35,39)(H,37,38)/t29-/m0/s1
• InChIKey: SLBNIPMLSUPCFW-LJAQVGFWSA-N
• SMILES: CN(C)C1=CC=CC2=C1C=CC=C2S(=O)(=O)NCCCC[C@@H](C(=O)O)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35

N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-((5-(dimethylamino)naphthalen-1-yl)sulfonyl)-L-lysine（Cat No.:M028476）is a complex, modified form of L-lysine, designed for use in peptide synthesis and biochemical research. The molecule features two distinct protective groups: a fluorenylmethoxycarbonyl (Fmoc) group at the N2 position and a sulfonyl group attached to a naphthalene ring with a dimethylamino group at the N6 position. These modifications serve to protect the lysine’s amino groups during peptide assembly, enabling selective removal of the protecting groups under specific conditions. This compound is useful in creating peptides with precise structural and functional properties.