Cyclohexanemethanamine, Nα-dimethyl-, (S)-, with the CAS number 138785-57-6, is an organic compound characterized by its chiral amine structure. It features a cyclohexane ring attached to a methanamine group, with two methyl groups on the nitrogen atom, contributing to its Nα-dimethyl designation. The (S)- prefix indicates that it has a specific stereochemistry, which can influence its biological activity and interactions. This compound is typically colorless to pale yellow and may exhibit a distinct amine odor. It is soluble in polar organic solvents and may have limited solubility in water. Cyclohexanemethanamine derivatives are often studied for their potential applications in pharmaceuticals, particularly as intermediates in the synthesis of biologically active compounds. The presence of the cyclohexane ring can impart unique steric and electronic properties, making it a subject of interest in medicinal chemistry and materials science. As with many amines, it may participate in various chemical reactions, including alkylation and acylation, and can act as a base in acid-base reactions.

Cyclohexanemethanamine, N,a-dimethyl-, (S)-

138785-57-6: Cyclohexanemethanamine, Nα-dimethyl-, (S)-, with the CAS number 138785-57-6, is an organic compound characterized by its chiral amine structure. It features a cyclohexane ring attached to a methanamine group, with two methyl groups on the nitrogen atom, contributing to its Nα-dimethyl designation. The (S)- prefix indicates that it has a specific stereochemistry, which can influence its biological activity and interactions. This compound is typically colorless to pale yellow and may exhibit a distinct amine odor. It is soluble in polar organic solvents and may have limited solubility in water. Cyclohexanemethanamine derivatives are often studied for their potential applications in pharmaceuticals, particularly as intermediates in the synthesis of biologically active compounds. The presence of the cyclohexane ring can impart unique steric and electronic properties, making it a subject of interest in medicinal chemistry and materials science. As with many amines, it may participate in various chemical reactions, including alkylation and acylation, and can act as a base in acid-base reactions.

CAS 138785-57-6

Cyclohexanemethanamine, N,a-dimethyl-, (S)-

[(1S)-1-cyclohexylethyl](methyl)amine

Ref: 3D-NFA78557