(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid

• CAT Number: I043144
• CAS Number: 220497-85-8
• Molecular Formula: C22H19NO5
• Molecular Weight: 377.39
• Purity: ≥95%
• Synonyms: (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(furan-2-yl)propanoic acid
• InChI: InChI=1S/C22H19NO5/c24-21(25)20(12-14-6-5-11-27-14)23-22(26)28-13-19-17-9-3-1-7-15(17)16-8-2-4-10-18(16)19/h1-11,19-20H,12-13H2,(H,23,26)(H,24,25)/t20-/m1/s1
• InChIKey: AJXDCHXGNUFBRC-HXUWFJFHSA-N
• SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@H](CC4=CC=CO4)C(=O)O

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(furan-2-yl)propanoic acid（Cat No.:I043144）is a chiral amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group on the amino group and a furan ring at the β-position. The Fmoc group is commonly used in solid-phase peptide synthesis (SPPS) to protect the amino functionality, allowing for selective deprotection during peptide assembly. The furan group introduces unique aromatic properties, which can be valuable in the development of bioactive molecules and peptides. This compound is useful in drug discovery and the design of peptides with specific interactions in biological pathways.