(2S)-2-Amino-2-[2-(trifluoromethyl)phenyl]ethan-1-ol hydrochloride is a chemical compound characterized by its amino alcohol structure, which features a chiral center at the second carbon atom. The presence of a trifluoromethyl group on the phenyl ring enhances its lipophilicity and may influence its biological activity. This compound is typically encountered as a hydrochloride salt, which improves its solubility in water and facilitates its handling in various applications. The amino group (-NH2) and hydroxyl group (-OH) contribute to its potential as a building block in pharmaceutical synthesis, particularly in the development of drugs targeting specific biological pathways. The trifluoromethyl group is known for imparting unique electronic properties, making this compound of interest in medicinal chemistry. Its stereochemistry, denoted by the (2S) configuration, is crucial for its interaction with biological targets, as enantiomers can exhibit significantly different pharmacological effects. Overall, this compound represents a valuable entity in the realm of organic synthesis and drug development.

(2S)-2-AMINO-2-[2-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL HYDROCHLORIDE

1391449-79-8: (2S)-2-Amino-2-[2-(trifluoromethyl)phenyl]ethan-1-ol hydrochloride is a chemical compound characterized by its amino alcohol structure, which features a chiral center at the second carbon atom. The presence of a trifluoromethyl group on the phenyl ring enhances its lipophilicity and may influence its biological activity. This compound is typically encountered as a hydrochloride salt, which improves its solubility in water and facilitates its handling in various applications. The amino group (-NH2) and hydroxyl group (-OH) contribute to its potential as a building block in pharmaceutical synthesis, particularly in the development of drugs targeting specific biological pathways. The trifluoromethyl group is known for imparting unique electronic properties, making this compound of interest in medicinal chemistry. Its stereochemistry, denoted by the (2S) configuration, is crucial for its interaction with biological targets, as enantiomers can exhibit significantly different pharmacological effects. Overall, this compound represents a valuable entity in the realm of organic synthesis and drug development.

CAS 1391449-79-8

(2S)-2-AMINO-2-[2-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL HYDROCHLORIDE

(S)-2-Amino-2-(2-(trifluoromethyl)phenyl)ethan-1-ol hydrochloride

Ref: IN-DA01XBL5

(S)-2-Amino-2-(2-(trifluoromethyl)phenyl)ethan-1-ol hydrochloride

Ref: 54-PC57466