(2S)-2-Amino-2-[4-chloro-3-(trifluoromethyl)phenyl]ethan-1-ol, with CAS number 1213059-76-7, is an organic compound characterized by its amino alcohol structure. It features a chiral center at the second carbon, which contributes to its stereochemistry. The presence of a 4-chloro-3-(trifluoromethyl)phenyl group indicates significant electron-withdrawing properties, which can influence the compound's reactivity and interactions with biological targets. The trifluoromethyl group enhances lipophilicity and can affect the compound's pharmacokinetic properties. This compound is likely to exhibit polar characteristics due to the hydroxyl (-OH) group, which can engage in hydrogen bonding. Its potential applications may include roles in medicinal chemistry, particularly in the development of pharmaceuticals, given its structural features that may interact with specific biological pathways. Overall, the compound's unique combination of functional groups and stereochemistry makes it a subject of interest in various chemical and biological studies.

(2S)-2-AMINO-2-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL

1213059-76-7: (2S)-2-Amino-2-[4-chloro-3-(trifluoromethyl)phenyl]ethan-1-ol, with CAS number 1213059-76-7, is an organic compound characterized by its amino alcohol structure. It features a chiral center at the second carbon, which contributes to its stereochemistry. The presence of a 4-chloro-3-(trifluoromethyl)phenyl group indicates significant electron-withdrawing properties, which can influence the compound's reactivity and interactions with biological targets. The trifluoromethyl group enhances lipophilicity and can affect the compound's pharmacokinetic properties. This compound is likely to exhibit polar characteristics due to the hydroxyl (-OH) group, which can engage in hydrogen bonding. Its potential applications may include roles in medicinal chemistry, particularly in the development of pharmaceuticals, given its structural features that may interact with specific biological pathways. Overall, the compound's unique combination of functional groups and stereochemistry makes it a subject of interest in various chemical and biological studies.

CAS 1213059-76-7

(2S)-2-AMINO-2-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL

(2S)-2-AMINO-2-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL

Ref: IN-DA009Z87

(S)-2-Amino-2-(4-chloro-3-(trifluoromethyl)phenyl)ethanol

Ref: 10-F455004