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CAS 83345-44-2

:

(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutanoic acid

Description:
(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutanoic acid, with the CAS number 83345-44-2, is an amino acid derivative characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group on the amino functional group. This compound features a chiral center at the 3-position, which contributes to its stereochemistry and potential biological activity. The hydroxy group at the 4-position enhances its solubility in polar solvents and may participate in hydrogen bonding, influencing its reactivity and interactions in biological systems. The Boc group serves as a protective moiety, commonly used in peptide synthesis to prevent unwanted reactions during the coupling of amino acids. This compound is typically utilized in organic synthesis and pharmaceutical applications, particularly in the development of peptide-based drugs. Its stability, solubility, and reactivity make it a valuable intermediate in the synthesis of more complex molecules. As with many amino acid derivatives, it may exhibit specific biological properties, including potential roles in metabolic pathways or as precursors to bioactive compounds.
Formula:C9H17NO5
InChI:InChI=1/C9H17NO5/c1-9(2,3)15-8(14)10-6(5-11)4-7(12)13/h6,11H,4-5H2,1-3H3,(H,10,14)(H,12,13)/t6-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](CC(=O)O)CO)O
Synonyms:
  • (3S)-3-[(tert-Butoxycarbonyl)amino]-4-hydroxybutanoic acid
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