BOC-(2R,3S)-2-amino-3-hydroxy-4-methylpentanoic acid, commonly referred to as BOC-AHMP, is a synthetic amino acid derivative characterized by its unique structural features. It contains a tert-butyloxycarbonyl (BOC) protecting group, which is commonly used in peptide synthesis to protect the amino group during chemical reactions. The compound has a chiral center, indicated by the (2R,3S) configuration, which contributes to its stereochemical properties and potential biological activity. The presence of both an amino group and a hydroxyl group in its structure allows for various interactions, making it a valuable building block in the synthesis of peptides and other bioactive molecules. BOC-AHMP is typically used in research and pharmaceutical applications, particularly in the development of compounds with specific biological functions. Its solubility and reactivity can vary depending on the solvent and conditions used, which is important for its application in organic synthesis. As with many amino acids, it may exhibit properties such as chirality, solubility in polar solvents, and potential for forming hydrogen bonds.

BOC-(2R,3S)-2-AMINO-3-HYDROXY-4-METHYLPENTANOIC ACID

182959-73-5: BOC-(2R,3S)-2-amino-3-hydroxy-4-methylpentanoic acid, commonly referred to as BOC-AHMP, is a synthetic amino acid derivative characterized by its unique structural features. It contains a tert-butyloxycarbonyl (BOC) protecting group, which is commonly used in peptide synthesis to protect the amino group during chemical reactions. The compound has a chiral center, indicated by the (2R,3S) configuration, which contributes to its stereochemical properties and potential biological activity. The presence of both an amino group and a hydroxyl group in its structure allows for various interactions, making it a valuable building block in the synthesis of peptides and other bioactive molecules. BOC-AHMP is typically used in research and pharmaceutical applications, particularly in the development of compounds with specific biological functions. Its solubility and reactivity can vary depending on the solvent and conditions used, which is important for its application in organic synthesis. As with many amino acids, it may exhibit properties such as chirality, solubility in polar solvents, and potential for forming hydrogen bonds.

CAS 182959-73-5

BOC-(2R,3S)-2-AMINO-3-HYDROXY-4-METHYLPENTANOIC ACID

(2R,3S)-2-((tert-Butoxycarbonyl)amino)-3-hydroxy-4-methylpentanoic acid

Ref: IN-DA00APCP

BOC-(2R,3S)-2-AMINO-3-HYDROXY-4-METHYLPENTANOIc acid

Ref: 10-F514130