(R)-N-(2,2-Difluoroethylidene)-1-phenylethylamine is a chiral amine characterized by its unique structural features, including a phenylethylamine backbone and a difluoroethylidene substituent. The presence of the difluoro group introduces significant electronegativity, which can influence the compound's reactivity and interaction with biological systems. As a chiral compound, it exists in two enantiomeric forms, with the (R) configuration being of particular interest in pharmaceutical applications due to its potential biological activity. The compound may exhibit properties such as moderate solubility in organic solvents and limited solubility in water, typical of many amines. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of selective ligands or inhibitors. Additionally, the difluoro group may enhance lipophilicity, affecting the compound's pharmacokinetics. Safety and handling considerations are essential, as with many fluorinated compounds, due to potential toxicity and environmental impact. Overall, this compound represents a valuable entity for further research in organic and medicinal chemistry.

(R)-N-(2,2-DIFLUOROETHYLIDENE)-1-PHENYLETHYLAMINE

160797-29-5: (R)-N-(2,2-Difluoroethylidene)-1-phenylethylamine is a chiral amine characterized by its unique structural features, including a phenylethylamine backbone and a difluoroethylidene substituent. The presence of the difluoro group introduces significant electronegativity, which can influence the compound's reactivity and interaction with biological systems. As a chiral compound, it exists in two enantiomeric forms, with the (R) configuration being of particular interest in pharmaceutical applications due to its potential biological activity. The compound may exhibit properties such as moderate solubility in organic solvents and limited solubility in water, typical of many amines. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of selective ligands or inhibitors. Additionally, the difluoro group may enhance lipophilicity, affecting the compound's pharmacokinetics. Safety and handling considerations are essential, as with many fluorinated compounds, due to potential toxicity and environmental impact. Overall, this compound represents a valuable entity for further research in organic and medicinal chemistry.

CAS 160797-29-5

(R)-N-(2,2-DIFLUOROETHYLIDENE)-1-PHENYLETHYLAMINE

(R)-N-(2,2-Difluoroethylidene)-1-phenylethylamine

Ref: IN-DA001VCL

(R)-N-(2,2-Difluoroethylidene)-1-phenylethylamine

Ref: 54-PC904768