For research use only. Not for therapeutic Use.
(S)-2-Amino-5-(tert-butoxy)-5-oxopentanoic acid(Cat No.:R061615)is a modified amino acid derivative commonly used in peptide synthesis. It features a tert-butoxy group at the 5-position of the pentanoic acid backbone, which provides steric protection and improves the stability of the compound during synthetic procedures. The 5-oxo group adds functional versatility, making it useful for further chemical modifications or conjugation reactions. The (S)-configuration of the amino group ensures stereochemical specificity during peptide formation. After synthesis, the tert-butoxy group can be removed under mild acidic conditions, allowing for further functionalization or elongation of peptides.
CAS Number | 2419-56-9 |
Synonyms | (2S)-2-amino-5-[(2-methylpropan-2-yl)oxy]-5-oxopentanoic acid |
Molecular Formula | C9H17NO4 |
Purity | ≥95% |
IUPAC Name | (2S)-2-amino-5-[(2-methylpropan-2-yl)oxy]-5-oxopentanoic acid |
InChI | InChI=1S/C9H17NO4/c1-9(2,3)14-7(11)5-4-6(10)8(12)13/h6H,4-5,10H2,1-3H3,(H,12,13)/t6-/m0/s1 |
InChIKey | OIOAKXPMBIZAHL-LURJTMIESA-N |
SMILES | CC(C)(C)OC(=O)CC[C@@H](C(=O)O)N |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |