The chemical substance known as (1S,2R)-2-(cyclohexylamino)-1,2-diphenylethanol, with the CAS number 142452-42-4, is a chiral compound characterized by its specific stereochemistry, indicated by the (1S,2R) configuration. This compound features a diphenylethanol backbone, which consists of two phenyl groups attached to a central ethyl chain that bears a hydroxyl (-OH) group. The presence of the cyclohexylamino group introduces a secondary amine functionality, contributing to its potential biological activity. The stereochemistry of this compound is crucial, as it can influence its interactions with biological targets, such as receptors or enzymes. Typically, compounds of this nature may exhibit properties such as solubility in organic solvents, moderate to high melting points, and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The specific arrangement of atoms and functional groups also suggests that it may participate in hydrogen bonding, which can affect its solubility and reactivity in various chemical environments.

(1S,2R)-2-(CYCLOHEXYLAMINO)-1,2-DIPHENYLETHANOL

142452-42-4: The chemical substance known as (1S,2R)-2-(cyclohexylamino)-1,2-diphenylethanol, with the CAS number 142452-42-4, is a chiral compound characterized by its specific stereochemistry, indicated by the (1S,2R) configuration. This compound features a diphenylethanol backbone, which consists of two phenyl groups attached to a central ethyl chain that bears a hydroxyl (-OH) group. The presence of the cyclohexylamino group introduces a secondary amine functionality, contributing to its potential biological activity. The stereochemistry of this compound is crucial, as it can influence its interactions with biological targets, such as receptors or enzymes. Typically, compounds of this nature may exhibit properties such as solubility in organic solvents, moderate to high melting points, and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The specific arrangement of atoms and functional groups also suggests that it may participate in hydrogen bonding, which can affect its solubility and reactivity in various chemical environments.

CAS 142452-42-4

(1S,2R)-2-(CYCLOHEXYLAMINO)-1,2-DIPHENYLETHANOL

(1S,2R)-2-(CYCLOHEXYLAMINO)-1,2-DIPHENYLETHANOL

Ref: IN-DA007L48

(1S,2R)-2-(Cyclohexylamino)-1,2-diphenylethanol

Ref: 10-F011657