(1R,2R)-(+)-N-(4-Toluenesulphonyl)-1,2-diaminocyclohexane is a chiral organic compound characterized by its specific stereochemistry, indicated by the (1R,2R) configuration. This compound features a cyclohexane ring with two amino groups (–NH2) at the 1 and 2 positions, which contribute to its potential as a ligand in coordination chemistry. The presence of the toluenesulphonyl group enhances its reactivity and solubility in organic solvents, making it useful in various synthetic applications. The sulphonyl group also serves as a protective group for amines, facilitating selective reactions. This compound is of interest in medicinal chemistry and asymmetric synthesis due to its chirality, which can influence biological activity and interaction with other molecules. Its CAS number, 174291-96-4, allows for easy identification in chemical databases. Overall, this compound exemplifies the intersection of organic synthesis and stereochemistry, highlighting its potential utility in developing pharmaceuticals and other fine chemicals.

(1R,2R)-(+)-N-(4-TOLUENESULPHONYL)-1,2-DIAMINOCYCLOHEXANE

174291-96-4: (1R,2R)-(+)-N-(4-Toluenesulphonyl)-1,2-diaminocyclohexane is a chiral organic compound characterized by its specific stereochemistry, indicated by the (1R,2R) configuration. This compound features a cyclohexane ring with two amino groups (–NH2) at the 1 and 2 positions, which contribute to its potential as a ligand in coordination chemistry. The presence of the toluenesulphonyl group enhances its reactivity and solubility in organic solvents, making it useful in various synthetic applications. The sulphonyl group also serves as a protective group for amines, facilitating selective reactions. This compound is of interest in medicinal chemistry and asymmetric synthesis due to its chirality, which can influence biological activity and interaction with other molecules. Its CAS number, 174291-96-4, allows for easy identification in chemical databases. Overall, this compound exemplifies the intersection of organic synthesis and stereochemistry, highlighting its potential utility in developing pharmaceuticals and other fine chemicals.

(1R,2R)-()-N-p-Tosyl-1,2-cyclohexanediamine

N-((1R,2R)-2-Aminocyclohexyl)-4-Methylbenzenesulfonamide

CAS 174291-96-4

(1R,2R)-(+)-N-(4-TOLUENESULPHONYL)-1,2-DIAMINOCYCLOHEXANE

(1R,2R)-()-N-p-Tosyl-1,2-cyclohexanediamine

Ref: IN-DA003BG4

N-((1R,2R)-2-Aminocyclohexyl)-4-Methylbenzenesulfonamide

Ref: 54-OR1013926

N-((1R,2R)-2-Aminocyclohexyl)-4-methylbenzenesulfonamide

Ref: 10-F547081