FMOC-GLU(OALL)-OH

• CAT Number: M115405
• CAS Number: 133464-46-7
• Molecular Formula: C23H23NO6
• Molecular Weight: 409.44
• Purity: ≥95%
• Storage: -20°C
• IUPAC Name: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-prop-2-enoxypentanoic acid
• InChI: InChI=1S/C23H23NO6/c1-2-13-29-21(25)12-11-20(22(26)27)24-23(28)30-14-19-17-9-5-3-7-15(17)16-8-4-6-10-18(16)19/h2-10,19-20H,1,11-14H2,(H,24,28)(H,26,27)/t20-/m0/s1
• InChIKey: LRBARFFNYOKIAX-FQEVSTJZSA-N
• SMILES: C=CCOC(=O)CCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

Fmoc-Glu(OAll)-OH（Cat No.:M115405） is a protected form of the amino acid glutamic acid, used in peptide synthesis. “Fmoc” stands for 9-fluorenyl methoxycarbonyl, a common protecting group for the amino group that can be removed under mild basic conditions without affecting other parts of the molecule. “Glu” refers to glutamic acid, and “(OAll)” indicates that the side chain carboxyl group is protected with an allyl ester (OAll). This protection can be removed through palladium-catalyzed deprotection methods. This specific compound allows for the selective deprotection of different parts during the synthesis process, facilitating the construction of complex peptide chains.