(S)-N-Fmoc-L-norleucine-13C6,15N

• CAT Number: R052204
• CAS Number: 1346617-52-4
• Molecular Formula: C21H23NO4
• Molecular Weight: 360.365
• Purity: ≥95%
• Synonyms: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-norleucine-13C6,15N; (S)-2-[[[(9H-Fluoren-9-yl)?methoxy]carbonyl]amino]hexanoic Acid-13C6,15N; (S)-N-Fmoc-norleucine-13C6,15N; FMOC-L-Norleucine-13C6,15N; Fmoc-norleucine-13C6,15N; N-(9-Fluorenyl-?methoxycarbony
• Storage: Room temperature
• IUPAC Name: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
• InChI: InChI=1S/C21H23NO4/c1-2-3-12-19(20(23)24)22-21(25)26-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,18-19H,2-3,12-13H2,1H3,(H,22,25)(H,23,24)/t19-/m0/s1/i1+1,2+1,3+1,12+1,19+1,20+1,22+1
• InChIKey: VCFCFPNRQDANPN-WPSJONIPSA-N
• SMILES: CCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

(S)-N-Fmoc-L-norleucine-13C6,15N is a deuterium-labeled derivative of (S)-N-Fmoc-L-norleucine, an amino acid commonly used in peptide synthesis. The 13C6 and 15N labels denote the presence of six carbon-13 and one nitrogen-15 isotopes, which enhance its utility in mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy by improving sensitivity and accuracy. This labeled compound is valuable for studying peptide synthesis and analyzing peptide structures, interactions, and conformations. It aids in the precise tracking of amino acids during peptide assembly and in the validation of synthetic methods and analytical techniques in peptide chemistry and related research.