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CAS 1149354-06-2

:

BOC-(S)-2-amino-2,4-dimethylpentanoicacid

Description:
BOC-(S)-2-amino-2,4-dimethylpentanoic acid, identified by its CAS number 1149354-06-2, is a chiral amino acid derivative characterized by the presence of a tert-butyloxycarbonyl (BOC) protecting group on the amino group. This compound features a branched aliphatic structure, with two methyl groups attached to the second carbon and one methyl group on the fourth carbon of the pentanoic acid backbone. The (S) configuration indicates that it has a specific stereochemistry, which is important for its biological activity and potential applications in pharmaceuticals and peptide synthesis. The BOC group serves as a protective moiety, allowing for selective reactions at the carboxylic acid or amine functionalities during synthetic processes. This compound is typically used in organic synthesis, particularly in the preparation of peptides, due to its ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino acid's chirality. Its solubility and reactivity can vary based on the solvent and conditions used in reactions.
Formula:C12H23NO4
Synonyms:
  • BOC-(S)-2-amino-2,4-dimethylpentanoicacid
  • (2S)-2-[(tert-butoxycarbonyl)amino]-2,4-dimethylpentanoic acid
  • L-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-2-methyl-
  • (S)-N-FMOC-N-BOC-Α-METHYLTRYPTOPHAN
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