(2,3-Difluoro-4-pyridinyl)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 3 positions. This compound typically exhibits properties associated with both boronic acids and pyridine derivatives, including moderate solubility in polar solvents and potential reactivity with various electrophiles due to the boronic acid moiety. The fluorine atoms can influence the electronic properties of the molecule, potentially enhancing its reactivity and stability. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in various applications, including organic synthesis and medicinal chemistry. The presence of the pyridine ring may also contribute to the compound's biological activity, as pyridine derivatives are often found in pharmaceuticals. Overall, (2,3-Difluoro-4-pyridinyl)boronic acid is a versatile compound with potential applications in drug development and materials science.

(2,3-Difluoro-4-pyridinyl)boronic acid

1263374-42-0: 2,3-Difluoropyridin-4-Ylboronic Acid, 2,3-Difluoropropyl Acetate, 1-Propanol,2,3-difluoro-,acetate

2,3-Difluoropyridine-4-boronic acid

(2,3-Difluoropyridin-4-yl)boronic acid

Boronic acid, B-(2,3-difluoro-4-pyridinyl)-

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CAS 1263374-42-0: (2,3-Difluoro-4-pyridinyl)boronic acid

2,3-Difluoropyridine-4-boronic acid

Ref: 54-PC412378

(2,3-Difluoropyridin-4-yl)boronic acid

Ref: 10-F498951

Boronic acid, B-(2,3-difluoro-4-pyridinyl)-

Ref: IN-DA000SNT

(2,3-Difluoropyridin-4-yl)boronic acid

Ref: 3D-FD160063