(2S,4S)-4-BOC-amino pyrrolidine-2-carboxylic acid methyl ester hydrochloride, with CAS number 1217779-15-1, is a chiral amino acid derivative characterized by its pyrrolidine ring structure. The "BOC" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, facilitating its use in peptide synthesis and other organic reactions. The compound features a carboxylic acid moiety, which is esterified with a methyl group, enhancing its solubility and reactivity. The hydrochloride salt form indicates the presence of hydrochloric acid, which improves the compound's stability and solubility in aqueous solutions. This substance is of interest in pharmaceutical chemistry, particularly in the development of biologically active compounds and as an intermediate in the synthesis of various pharmaceuticals. Its stereochemistry, denoted by the (2S,4S) configuration, is crucial for its biological activity, as the spatial arrangement of atoms can significantly influence the compound's interactions with biological targets.

(2S,4S)-4-BOC-aMino Pyrrolidine-2-carboxylic acid Methylester-HCl

1217779-15-1: (2S,4S)-4-BOC-amino pyrrolidine-2-carboxylic acid methyl ester hydrochloride, with CAS number 1217779-15-1, is a chiral amino acid derivative characterized by its pyrrolidine ring structure. The "BOC" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, facilitating its use in peptide synthesis and other organic reactions. The compound features a carboxylic acid moiety, which is esterified with a methyl group, enhancing its solubility and reactivity. The hydrochloride salt form indicates the presence of hydrochloric acid, which improves the compound's stability and solubility in aqueous solutions. This substance is of interest in pharmaceutical chemistry, particularly in the development of biologically active compounds and as an intermediate in the synthesis of various pharmaceuticals. Its stereochemistry, denoted by the (2S,4S) configuration, is crucial for its biological activity, as the spatial arrangement of atoms can significantly influence the compound's interactions with biological targets.

CAS 1217779-15-1

(2S,4S)-4-BOC-aMino Pyrrolidine-2-carboxylic acid Methylester-HCl

(2S,4S)-Methyl 4-((tert-butoxycarbonyl)amino)pyrrolidine-2-carboxylate hydrochloride

Ref: IN-DA009GS0