(R)-(+)-1-(4-Cyanophenyl)ethylamine is an organic compound characterized by its chiral structure, which includes a phenyl group substituted with a cyano group at the para position relative to the ethylamine moiety. This compound features a stereocenter, contributing to its enantiomeric form, which is significant in various applications, particularly in pharmaceuticals and organic synthesis. The presence of the cyano group enhances its reactivity and polarity, making it useful in various chemical reactions, including nucleophilic substitutions and as a building block in the synthesis of more complex molecules. The amine functional group imparts basic properties, allowing it to participate in acid-base reactions. Additionally, the compound's solubility characteristics can vary based on the solvent used, influencing its application in different chemical environments. Overall, (R)-(+)-1-(4-Cyanophenyl)ethylamine is notable for its potential in medicinal chemistry and as a chiral auxiliary in asymmetric synthesis.

(R)-(+)-1-(4-Cyanophenyl)ethylamine

210488-53-2: 4-[(1S)-1-aminoethyl]benzonitrile

(R)-1-(4-Cyanophenyl)ethylamine

(R)-4-(1-Aminoethyl)benzonitrile

Benzonitrile, 4-[(1R)-1-aminoethyl]-

This product is an enantioselective chiral reagent that can be used in biotransformations. It reacts with microorganisms to produce biologically active inositol phosphates. The product has been shown to be an innovative laboratory reagent for the preparation of chiral, enantiomerically pure phosphates. This product also has lipase-catalyzed reactions to produce enantiomerically pure lipids from a variety of substrates.

CAS 210488-53-2: (R)-(+)-1-(4-Cyanophenyl)ethylamine

(R)-1-(4-Cyanophenyl)ethylamine

Ref: 10-F208985

(R)-4-(1-Aminoethyl)benzonitrile

Ref: 54-OR77235

Benzonitrile, 4-[(1R)-1-aminoethyl]-

Ref: IN-DA002KTA

4-[(1R)-1-Aminoethyl]-benzonitrile

Ref: 3D-FA151222