6,6,6-Trifluoro-5-oxohexanoic acid is a fluorinated organic compound characterized by the presence of three fluorine atoms, a ketone functional group, and a carboxylic acid group. Its molecular structure features a six-carbon chain with a ketone located at the fifth carbon and a carboxylic acid at the terminal position. The trifluoromethyl group significantly influences its chemical properties, enhancing its acidity and reactivity compared to non-fluorinated analogs. This compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its fluorinated nature can impart unique characteristics such as increased lipophilicity and stability against metabolic degradation. Additionally, the presence of the carboxylic acid group allows for potential interactions in various chemical reactions, including esterification and amidation. Safety data should be consulted for handling, as fluorinated compounds can exhibit specific toxicological profiles. Overall, 6,6,6-trifluoro-5-oxohexanoic acid is notable for its unique structural features and potential applications in chemical synthesis.

6,6,6-trifluoro-5-oxohexanoic acid

184157-09-3: 6,6,6-Trifluoro-5-oxohexanoic acid is a fluorinated organic compound characterized by the presence of three fluorine atoms, a ketone functional group, and a carboxylic acid group. Its molecular structure features a six-carbon chain with a ketone located at the fifth carbon and a carboxylic acid at the terminal position. The trifluoromethyl group significantly influences its chemical properties, enhancing its acidity and reactivity compared to non-fluorinated analogs. This compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its fluorinated nature can impart unique characteristics such as increased lipophilicity and stability against metabolic degradation. Additionally, the presence of the carboxylic acid group allows for potential interactions in various chemical reactions, including esterification and amidation. Safety data should be consulted for handling, as fluorinated compounds can exhibit specific toxicological profiles. Overall, 6,6,6-trifluoro-5-oxohexanoic acid is notable for its unique structural features and potential applications in chemical synthesis.

CAS 184157-09-3

6,6,6-trifluoro-5-oxohexanoic acid

6,6,6-Trifluoro-5-oxohexanoic acid

Ref: 54-PC111782

5-Oxo-6,6,6-trifluorohexanoic acid

Ref: 10-F207276