The chemical substance known as (1S,2R,4S)-2-(hydroxymethyl)-4-phenylcyclohexanaminium, with the CAS number 195190-88-6, is a chiral amine characterized by its cyclohexane ring structure, which includes a hydroxymethyl group and a phenyl substituent. This compound exhibits basic properties due to the presence of the aminium group, making it capable of forming salts with acids. Its stereochemistry, indicated by the (1S,2R,4S) configuration, suggests specific spatial arrangements of its atoms, which can influence its reactivity and interactions with biological systems. The presence of the hydroxymethyl group contributes to its potential solubility in polar solvents, while the phenyl group may enhance hydrophobic interactions. Such structural features may also impart biological activity, making it of interest in medicinal chemistry. Overall, this compound's unique characteristics stem from its stereochemistry and functional groups, which can affect its physical and chemical properties, as well as its potential applications in pharmaceuticals or as a biochemical probe.

(1S,2R,4S)-2-(hydroxymethyl)-4-phenylcyclohexanaminium

195190-88-6: The chemical substance known as (1S,2R,4S)-2-(hydroxymethyl)-4-phenylcyclohexanaminium, with the CAS number 195190-88-6, is a chiral amine characterized by its cyclohexane ring structure, which includes a hydroxymethyl group and a phenyl substituent. This compound exhibits basic properties due to the presence of the aminium group, making it capable of forming salts with acids. Its stereochemistry, indicated by the (1S,2R,4S) configuration, suggests specific spatial arrangements of its atoms, which can influence its reactivity and interactions with biological systems. The presence of the hydroxymethyl group contributes to its potential solubility in polar solvents, while the phenyl group may enhance hydrophobic interactions. Such structural features may also impart biological activity, making it of interest in medicinal chemistry. Overall, this compound's unique characteristics stem from its stereochemistry and functional groups, which can affect its physical and chemical properties, as well as its potential applications in pharmaceuticals or as a biochemical probe.

CAS 195190-88-6

(1S,2R,4S)-2-(hydroxymethyl)-4-phenylcyclohexanaminium

2-cis-Hydroxymethyl-4-trans-phenyl-1-cyclohexylamine

Ref: IN-DA003878

cis-(2-Amino-trans-5-phenyl-cyclohexyl)-methanol

Ref: 54-OR309429