Rel-(1R,3S)-3-[(Phenylmethyl)amino]cyclohexanol, identified by its CAS number 1089695-63-5, is a chiral organic compound characterized by its cyclohexanol backbone, which features a phenylmethylamino substituent. This compound exhibits stereochemistry, with specific configurations at the 1 and 3 positions of the cyclohexanol ring, contributing to its potential biological activity and interactions. The presence of the phenylmethyl group enhances its lipophilicity, which may influence its solubility and permeability in biological systems. As a secondary amine, it can participate in hydrogen bonding and may interact with various biological targets, making it of interest in medicinal chemistry. The compound's structural features suggest potential applications in pharmaceuticals, particularly in the development of drugs targeting the central nervous system or other therapeutic areas. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its properties can be further explored through spectroscopic methods and biological assays to determine its efficacy and safety profiles.

rel-(1R,3S)-3-[(Phenylmethyl)amino]cyclohexanol

1089695-63-5: Rel-(1R,3S)-3-[(Phenylmethyl)amino]cyclohexanol, identified by its CAS number 1089695-63-5, is a chiral organic compound characterized by its cyclohexanol backbone, which features a phenylmethylamino substituent. This compound exhibits stereochemistry, with specific configurations at the 1 and 3 positions of the cyclohexanol ring, contributing to its potential biological activity and interactions. The presence of the phenylmethyl group enhances its lipophilicity, which may influence its solubility and permeability in biological systems. As a secondary amine, it can participate in hydrogen bonding and may interact with various biological targets, making it of interest in medicinal chemistry. The compound's structural features suggest potential applications in pharmaceuticals, particularly in the development of drugs targeting the central nervous system or other therapeutic areas. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its properties can be further explored through spectroscopic methods and biological assays to determine its efficacy and safety profiles.

CAS 1089695-63-5

rel-(1R,3S)-3-[(Phenylmethyl)amino]cyclohexanol