2-(Benzyl(methyl)amino)-1-phenylethanol, identified by its CAS number 895573-64-5, is an organic compound characterized by its complex structure featuring both an alcohol and an amine functional group. This compound typically exhibits a chiral center, which can lead to the existence of enantiomers, potentially influencing its biological activity and interactions. The presence of the benzyl and phenyl groups contributes to its hydrophobic characteristics, while the hydroxyl group enhances its solubility in polar solvents. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its synthesis often involves multi-step organic reactions, and it may serve as an intermediate in the development of pharmaceuticals or other biologically active compounds. Additionally, its stability and reactivity can be influenced by the surrounding environment, such as pH and temperature, which are important considerations in both laboratory and industrial applications. Overall, 2-(benzyl(methyl)amino)-1-phenylethanol represents a versatile structure with potential applications in various fields of chemistry and biochemistry.

2-(benzyl(methyl)amino)-1-phenylethanol

895573-64-5: 2-(Benzyl(methyl)amino)-1-phenylethanol, identified by its CAS number 895573-64-5, is an organic compound characterized by its complex structure featuring both an alcohol and an amine functional group. This compound typically exhibits a chiral center, which can lead to the existence of enantiomers, potentially influencing its biological activity and interactions. The presence of the benzyl and phenyl groups contributes to its hydrophobic characteristics, while the hydroxyl group enhances its solubility in polar solvents. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its synthesis often involves multi-step organic reactions, and it may serve as an intermediate in the development of pharmaceuticals or other biologically active compounds. Additionally, its stability and reactivity can be influenced by the surrounding environment, such as pH and temperature, which are important considerations in both laboratory and industrial applications. Overall, 2-(benzyl(methyl)amino)-1-phenylethanol represents a versatile structure with potential applications in various fields of chemistry and biochemistry.

CAS 895573-64-5

2-(benzyl(methyl)amino)-1-phenylethanol

3-(5-methyl-1,2,4-oxadiazol-3-yl)piperidine

Ref: IN-DA003ZMT