(2R)-2-Amino-2-(4-bromo-2-fluorophenyl)ethan-1-ol, with the CAS number 1212983-75-9, is an organic compound characterized by its amino alcohol structure. It features a chiral center at the second carbon, which contributes to its stereochemistry, specifically the (2R) configuration. The presence of a bromine and a fluorine atom on the phenyl ring enhances its reactivity and potential biological activity, making it of interest in medicinal chemistry. This compound is likely to exhibit polar characteristics due to the hydroxyl (-OH) group, which can engage in hydrogen bonding, influencing its solubility in polar solvents. Additionally, the amino group (-NH2) can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The unique combination of halogen substituents may also impart specific electronic properties, affecting its interaction with biological targets. Overall, this compound's structural features suggest potential applications in pharmaceuticals, particularly in the development of drugs targeting specific receptors or enzymes.

(2R)-2-AMINO-2-(4-BROMO-2-FLUOROPHENYL)ETHAN-1-OL

1212983-75-9: (2R)-2-Amino-2-(4-bromo-2-fluorophenyl)ethan-1-ol, with the CAS number 1212983-75-9, is an organic compound characterized by its amino alcohol structure. It features a chiral center at the second carbon, which contributes to its stereochemistry, specifically the (2R) configuration. The presence of a bromine and a fluorine atom on the phenyl ring enhances its reactivity and potential biological activity, making it of interest in medicinal chemistry. This compound is likely to exhibit polar characteristics due to the hydroxyl (-OH) group, which can engage in hydrogen bonding, influencing its solubility in polar solvents. Additionally, the amino group (-NH2) can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The unique combination of halogen substituents may also impart specific electronic properties, affecting its interaction with biological targets. Overall, this compound's structural features suggest potential applications in pharmaceuticals, particularly in the development of drugs targeting specific receptors or enzymes.

(R)-2-Amino-2-(4-bromo-2-fluorophenyl)ethan-1-ol

CAS 1212983-75-9

(2R)-2-AMINO-2-(4-BROMO-2-FLUOROPHENYL)ETHAN-1-OL

(R)-2-Amino-2-(4-bromo-2-fluorophenyl)ethan-1-ol

Ref: 54-PC1006545