(αS,3S)-α-[(tert-Butyloxycarbonyl)aMino]-2-oxo-3-pyrrolidinepropanoic acid Methyl Ester CAS:328086-60-8

The molecule features a pyrrolidine ring, a five-membered saturated nitrogen-containing heterocycle. This ring is attached to a propanoic acid moiety, which includes a carboxyl group (-COOH). The presence of the carboxyl group makes the compound acidic and capable of forming salts or esters. An amino group (-NH2) is also present, but it is protected by a tert-butyloxycarbonyl (BOC) protecting group, which prevents it from participating in reactions. This protection is often used in synthetic chemistry to ensure that the amino group remains intact until the desired reaction is carried out. The (αS,3S) configuration indicates that the molecule has two chiral centers, one at the alpha position of the carboxyl group and the other at the 3-position of the pyrrolidine ring. The absolute configurations of these centers determine the spatial arrangement of the atoms and can influence the molecule's biological activity and reactivity. Overall, this compound is likely to be of interest in the fields of organic synthesis and medicinal chemistry, where its protected amino group and functionalized pyrrolidine ring can be used to construct more complex molecules with potential therapeutic applications.