For research use only. Not for therapeutic Use.
(S)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid(Cat No.:R059433)is a modified amino acid derivative used in peptide synthesis. It features a tert-butoxycarbonyl (Boc) protective group on the amino group, which prevents side reactions and ensures controlled peptide chain assembly. The compound also contains a pent-4-enoic acid structure with an unsaturated alkene group, providing opportunities for further chemical modifications or conjugation reactions. The Boc group can be removed under mild acidic conditions, revealing the free amino group for further peptide elongation or functionalization. This compound is valuable for advanced synthetic chemistry and drug development applications.
CAS Number | 90600-20-7 |
Synonyms | (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pent-4-enoic acid |
Molecular Formula | C10H17NO4 |
Purity | ≥95% |
IUPAC Name | (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pent-4-enoic acid |
InChI | InChI=1S/C10H17NO4/c1-5-6-7(8(12)13)11-9(14)15-10(2,3)4/h5,7H,1,6H2,2-4H3,(H,11,14)(H,12,13)/t7-/m0/s1 |
InChIKey | BUPDPLXLAKNJMI-ZETCQYMHSA-N |
SMILES | CC(C)(C)OC(=O)N[C@@H](CC=C)C(=O)O |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |