(2S,4R)-1-((S)-2-((tert-butoxycarbonyl)amino)non-8-enoyl)-4-hydroxypyrrolidine-2-carboxylic acid

• CAT Number: I043093
• CAS Number: 552335-47-4
• Molecular Formula: C19H32N2O6
• Molecular Weight: 384.47
• Purity: ≥95%
• Synonyms: (2S,4R)-4-hydroxy-1-[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]non-8-enoyl]pyrrolidine-2-carboxylic acid
• InChI: InChI=1S/C19H32N2O6/c1-5-6-7-8-9-10-14(20-18(26)27-19(2,3)4)16(23)21-12-13(22)11-15(21)17(24)25/h5,13-15,22H,1,6-12H2,2-4H3,(H,20,26)(H,24,25)/t13-,14+,15+/m1/s1
• InChIKey: OMMAVELVJUFTFD-ILXRZTDVSA-N
• SMILES: CC(C)(C)OC(=O)N[C@@H](CCCCCC=C)C(=O)N1C[C@@H](C[C@H]1C(=O)O)O

(2S,4R)-1-((S)-2-((tert-Butoxycarbonyl)amino)non-8-enoyl)-4-hydroxypyrrolidine-2-carboxylic acid（Cat No.:I043093）is a complex Boc-protected amino acid derivative used in peptide synthesis and pharmaceutical research. The pyrrolidine ring enhances rigidity, influencing peptide conformation, while the hydroxyl group provides additional functional versatility. The tert-butoxycarbonyl (Boc) group protects the amine, enabling controlled deprotection in synthetic pathways. Its non-8-enoyl side chain adds hydrophobic character, making it valuable in drug discovery, bioactive peptide synthesis, and enzyme inhibitor development. This compound plays a crucial role in designing structurally constrained peptides for medicinal and biochemical applications.