N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N5,N5-dimethyl-L-glutamine

• CAT Number: I043109
• CAS Number: 1146118-59-3
• Molecular Formula: C22H24N2O5
• Molecular Weight: 396.44
• Purity: ≥95%
• Synonyms: (2S)-5-(dimethylamino)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxopentanoic acid
• InChI: InChI=1S/C22H24N2O5/c1-24(2)20(25)12-11-19(21(26)27)23-22(28)29-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h3-10,18-19H,11-13H2,1-2H3,(H,23,28)(H,26,27)/t19-/m0/s1
• InChIKey: RSMCAOKIIZQPSD-IBGZPJMESA-N
• SMILES: CN(C)C(=O)CC[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N5,N5-dimethyl-L-glutamine（Cat No.:I043109）is a modified form of L-glutamine, featuring a fluorenylmethoxycarbonyl (Fmoc) protective group at the N2 position and two methyl groups at the N5 position. The Fmoc group is commonly used in peptide synthesis as a reversible protecting group for the amino functionality, preventing undesired reactions during peptide chain elongation. The dimethylation at N5 adds steric bulk, potentially influencing the compound’s interaction with enzymes or receptors. This derivative is valuable in peptide synthesis, particularly in creating peptides with specific functional properties or studying glutamine’s role in cellular processes.