FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLY-OH

• CAT Number: M097962
• CAS Number: 141743-15-9
• Molecular Formula: C24H28N2O6
• Molecular Weight: 440.496
• Purity: ≥95%
• Storage: Store at -80C
• IUPAC Name: 2-[9H-fluoren-9-ylmethoxycarbonyl-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethyl]amino]acetic acid
• InChI: InChI=1S/C24H28N2O6/c1-24(2,3)32-22(29)25-12-13-26(14-21(27)28)23(30)31-15-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,20H,12-15H2,1-3H3,(H,25,29)(H,27,28)
• InChIKey: SMLJSDLXJRGOKW-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NCCN(CC(=O)O)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

FMOC-N-(N-BETA-BOC-AMINOETHYL)-GLY-OH(CAT: M097962) is a chemical compound utilized in peptide synthesis and protection strategies. Its action target involves the modification and protection of amino acids during peptide assembly. The mode of action includes the addition of the FMOC (9-fluorenylmethoxycarbonyl) protecting group to the amine of N-(N-beta-boc-aminoethyl)-glycine, shielding it from unwanted reactions during peptide synthesis. Pharmacologically, FMOC-N-(N-beta-boc-aminoethyl)-glycine itself does not have direct medical applications. Instead, it plays a crucial role in solid-phase peptide synthesis, allowing the stepwise assembly of peptides with specific sequences. It is commonly used in custom peptide synthesis for research, drug discovery, and biochemical studies.