(2,5-Difluoropyridin-4-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has two fluorine substituents at the 2 and 5 positions. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and having moderate stability under standard conditions. The presence of the boronic acid group allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The fluorine atoms can influence the electronic properties of the molecule, potentially enhancing its reactivity and selectivity in chemical transformations. Additionally, the compound may exhibit interesting biological activities, which can be explored in pharmaceutical applications. Overall, (2,5-difluoropyridin-4-yl)boronic acid serves as a versatile building block in the development of complex organic molecules.

(2,5-difluoropyridin-4-yl)boronic acid

1263375-23-0: 2,5-Difluoropyridin-4-Ylboronic Acid, 2,5-Difluoropyridine-4-boronic acid

2,5-Difluoropyridine-4-boronic acid

Boronic acid, B-(2,5-difluoro-4-pyridinyl)-

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CAS 1263375-23-0: (2,5-difluoropyridin-4-yl)boronic acid

2,5-Difluoropyridine-4-boronic acid

Ref: 54-PC412380

Boronic acid, B-(2,5-difluoro-4-pyridinyl)-

Ref: IN-DA000SNS

(2,5-Difluoropyridin-4-yl)boronic acid

Ref: 3D-FD160064

2,5-DIFLUOROPYRIDIN-4-YLBORONIC ACID

Ref: 10-F301767