(S)-BOC-2-amino-3-(3-indolyl)-propionitrile, with the CAS number 138165-79-4, is a chemical compound characterized by its chiral nature, featuring a BOC (tert-butyloxycarbonyl) protecting group on the amino group. This compound contains an indole moiety, which contributes to its potential biological activity, particularly in medicinal chemistry. The presence of the propionitrile functional group indicates that it has a nitrile (-C≡N) group, which can participate in various chemical reactions, including nucleophilic additions and cycloadditions. The BOC group is commonly used in peptide synthesis as a temporary protecting group for amines, allowing for selective reactions without affecting the amino functionality. This compound is of interest in the development of pharmaceuticals, particularly in the context of drug design targeting specific biological pathways. Its stereochemistry is crucial for its biological activity, as the (S) configuration can influence the interaction with biological targets, such as enzymes or receptors. Overall, (S)-BOC-2-amino-3-(3-indolyl)-propionitrile is a versatile compound with significant implications in organic synthesis and drug development.

(S)-BOC-2-AMINO-3-(3-INDOLYL)-PROPIONITRILE

138165-79-4: (S)-BOC-2-amino-3-(3-indolyl)-propionitrile, with the CAS number 138165-79-4, is a chemical compound characterized by its chiral nature, featuring a BOC (tert-butyloxycarbonyl) protecting group on the amino group. This compound contains an indole moiety, which contributes to its potential biological activity, particularly in medicinal chemistry. The presence of the propionitrile functional group indicates that it has a nitrile (-C≡N) group, which can participate in various chemical reactions, including nucleophilic additions and cycloadditions. The BOC group is commonly used in peptide synthesis as a temporary protecting group for amines, allowing for selective reactions without affecting the amino functionality. This compound is of interest in the development of pharmaceuticals, particularly in the context of drug design targeting specific biological pathways. Its stereochemistry is crucial for its biological activity, as the (S) configuration can influence the interaction with biological targets, such as enzymes or receptors. Overall, (S)-BOC-2-amino-3-(3-indolyl)-propionitrile is a versatile compound with significant implications in organic synthesis and drug development.

CAS 138165-79-4

(S)-BOC-2-AMINO-3-(3-INDOLYL)-PROPIONITRILE

Boc-(s)-2-amino-3-(3-indolyl)-propionitrile

Ref: IN-DA001836

(S)-tert-Butyl (1-cyano-2-(1H-indol-3-yl)ethyl)carbamate

Ref: 10-F436081