5,5-Difluoropiperidine-2-carboxylic acid is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The presence of two fluorine atoms at the 5-position of the piperidine ring significantly influences its chemical properties, including increased lipophilicity and potential reactivity. The carboxylic acid functional group at the 2-position contributes to its acidity and ability to participate in various chemical reactions, such as esterification and amidation. This compound may exhibit biological activity, making it of interest in pharmaceutical research and development. Its molecular structure allows for potential interactions with biological targets, which can be explored for therapeutic applications. Additionally, the fluorine substituents can enhance metabolic stability and alter the pharmacokinetic profile of derivatives. As with many fluorinated compounds, 5,5-difluoropiperidine-2-carboxylic acid may also exhibit unique properties in terms of solubility and reactivity, making it a valuable compound in synthetic organic chemistry and medicinal chemistry.

5,5-difluoropiperidine-2-carboxylic acid

1255663-89-8: 5,5-Difluoropiperidine-2-carboxylic acid is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The presence of two fluorine atoms at the 5-position of the piperidine ring significantly influences its chemical properties, including increased lipophilicity and potential reactivity. The carboxylic acid functional group at the 2-position contributes to its acidity and ability to participate in various chemical reactions, such as esterification and amidation. This compound may exhibit biological activity, making it of interest in pharmaceutical research and development. Its molecular structure allows for potential interactions with biological targets, which can be explored for therapeutic applications. Additionally, the fluorine substituents can enhance metabolic stability and alter the pharmacokinetic profile of derivatives. As with many fluorinated compounds, 5,5-difluoropiperidine-2-carboxylic acid may also exhibit unique properties in terms of solubility and reactivity, making it a valuable compound in synthetic organic chemistry and medicinal chemistry.

CAS 1255663-89-8

5,5-difluoropiperidine-2-carboxylic acid

5,5-Difluoro-2-piperidinecarboxylic acid

Ref: IN-DA000NVW

5,5-DIFLUORO-2-PIPERIDINECARBOXYLIC ACID

Ref: 10-F467672