FMOC-ALA-GLY-OH

• CAT Number: M027070
• CAS Number: 116747-54-7
• Molecular Formula: C20H20N2O5
• Molecular Weight: 368.39
• Purity: ≥95%
• Storage: Desiccate at +4℃
• IUPAC Name: 2-[[(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoyl]amino]acetic acid
• InChI: InChI=1S/C20H20N2O5/c1-12(19(25)21-10-18(23)24)22-20(26)27-11-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,12,17H,10-11H2,1H3,(H,21,25)(H,22,26)(H,23,24)/t12-/m0/s1
• InChIKey: GOCNEQGFDAXBQE-LBPRGKRZSA-N
• SMILES: CC(C(=O)NCC(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

Fmoc-Ala-Gly-OH (Cat No.: M027070) is a protected dipeptide composed of alanine and glycine, with the N-terminal amino group protected by a 9-fluorenylmethyloxycarbonyl (Fmoc) group. This compound is commonly used in solid-phase peptide synthesis (SPPS) to build longer peptide chains in a controlled, stepwise manner. The Fmoc group allows for mild, base-labile deprotection without affecting other protective groups. Fmoc-Ala-Gly-OH is useful in structure–activity relationship studies, peptide drug design, and biochemical research involving sequence-specific interactions or folding studies.