3,5-Difluoropyridine-2-carboxylic acid is a heterocyclic organic compound characterized by a pyridine ring substituted with two fluorine atoms at the 3 and 5 positions and a carboxylic acid group at the 2 position. This compound typically exhibits a polar nature due to the presence of the carboxylic acid functional group, which can engage in hydrogen bonding, influencing its solubility in polar solvents like water. The fluorine substituents enhance the compound's reactivity and lipophilicity, making it of interest in various chemical syntheses and pharmaceutical applications. Its molecular structure contributes to its potential as an intermediate in the synthesis of agrochemicals and pharmaceuticals. The compound's properties, such as melting point, boiling point, and spectral characteristics, can vary based on environmental conditions and purity. As with many fluorinated compounds, it may exhibit unique electronic properties, making it valuable in materials science and medicinal chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

3,5-Difluoropyridine-2-carboxylic acid

745784-04-7: 2-Pyridinecarboxylic acid, 3,5-difluoro-, 3,5-Difluoro-2-pyridinecarboxylic acid, 3,5-Difluoropicolinic acid, 3,5-Difluoropyridine-2-carboxylic acid

3,5-difluoropyridine-2-carboxylic acid

3,5-Difluoropyridine-2-carboxylic acid is the carboxylate form of 3,5-difluoropyridine. It has been used in the synthesis of antidiabetic drugs and devices. This compound is a ligand for a number of metal ions. 3,5-Difluoropyridine-2-carboxylic acid undergoes uptake by rat adipocytes and has been shown to be crystallographically active.

CAS 745784-04-7: 3,5-Difluoropyridine-2-carboxylic acid

3,5-difluoropyridine-2-carboxylic acid

Ref: IN-DA0036IT

3,5-Difluoropyridine-2-carboxylic acid

Ref: 54-PC10530

3,5-difluoropyridine-2-carboxylic Acid

Ref: 3D-FD104686

3,5-Difluoropyridine-2-carboxylic acid

Ref: 10-F046203