(S)-4,4,4-Trifluoro-3-hydroxybutyric acid is a fluorinated organic compound characterized by the presence of three fluorine atoms and a hydroxyl group attached to a butyric acid backbone. This compound is notable for its unique trifluoromethyl group, which significantly influences its chemical reactivity and physical properties. The presence of the hydroxyl group contributes to its potential as a chiral building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The trifluoromethyl group enhances lipophilicity and can improve the metabolic stability of derivatives. This compound is typically used in research settings, particularly in studies related to fluorinated compounds and their applications in medicinal chemistry. Its chiral nature allows for the exploration of stereochemistry in reactions, making it a valuable tool in asymmetric synthesis. Safety data should be consulted for handling, as fluorinated compounds can exhibit unique toxicological profiles. Overall, (S)-4,4,4-trifluoro-3-hydroxybutyric acid represents a significant compound in the field of synthetic organic chemistry.

(S)-4,4,4-TRIFLUORO-3-HYDROXYBUTYRIC ACID

128899-79-6: (S)-4,4,4-Trifluoro-3-hydroxybutyric acid is a fluorinated organic compound characterized by the presence of three fluorine atoms and a hydroxyl group attached to a butyric acid backbone. This compound is notable for its unique trifluoromethyl group, which significantly influences its chemical reactivity and physical properties. The presence of the hydroxyl group contributes to its potential as a chiral building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The trifluoromethyl group enhances lipophilicity and can improve the metabolic stability of derivatives. This compound is typically used in research settings, particularly in studies related to fluorinated compounds and their applications in medicinal chemistry. Its chiral nature allows for the exploration of stereochemistry in reactions, making it a valuable tool in asymmetric synthesis. Safety data should be consulted for handling, as fluorinated compounds can exhibit unique toxicological profiles. Overall, (S)-4,4,4-trifluoro-3-hydroxybutyric acid represents a significant compound in the field of synthetic organic chemistry.

CAS 128899-79-6

(S)-4,4,4-TRIFLUORO-3-HYDROXYBUTYRIC ACID

(S)-4,4,4-Trifluoro-3-hydroxybutyric acid

Ref: IN-DA000YHE

(3S)-3-Hydroxy-4,4,4-trifluorobutanoic acid

Ref: 54-PC0622