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

• CAT Number: I043132
• CAS Number: 220497-90-5
• Molecular Formula: C22H19NO4S
• Molecular Weight: 393.46
• Purity: ≥95%
• Synonyms: (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-thiophen-3-ylpropanoic acid
• InChI: InChI=1S/C22H19NO4S/c24-21(25)20(11-14-9-10-28-13-14)23-22(26)27-12-19-17-7-3-1-5-15(17)16-6-2-4-8-18(16)19/h1-10,13,19-20H,11-12H2,(H,23,26)(H,24,25)/t20-/m1/s1
• InChIKey: LSBZJMRHROCYGY-HXUWFJFHSA-N
• SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@H](CC4=CSC=C4)C(=O)O

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(thiophen-3-yl)propanoic acid（Cat  No.:I043132）is a synthetic compound with a chiral center at the 2-position, making it the (R)-enantiomer. It features a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis, along with a thiophene ring at the 3-position of a propanoic acid backbone. This compound combines aromatic and sulfur-containing structures, offering potential bioactivity in medicinal chemistry, particularly in drug development and peptide chemistry. It may serve as a building block in drug design, targeting specific receptor or enzyme interactions.