(5-Bromo-3-fluoropyridin-2-yl)methanol is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of bromine and fluorine substituents at the 5 and 3 positions, respectively, contributes to its unique reactivity and physical properties. The hydroxymethyl group (-CH2OH) attached to the nitrogen-containing ring enhances its potential for hydrogen bonding, making it soluble in polar solvents. This compound may exhibit biological activity due to its structural features, which can interact with various biological targets. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Additionally, the presence of halogen atoms can influence the compound's lipophilicity and metabolic stability. As with many halogenated compounds, safety and environmental considerations are important, as they may pose risks during synthesis and disposal. Overall, (5-bromo-3-fluoropyridin-2-yl)methanol is a versatile compound with significant implications in chemical research and application.

(5-bromo-3-fluoropyridin-2-yl)methanol

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(5-Bromo-3-fluoropyridin-2-yl)methanol

5-Bromo-3-fluoro-2-(hydroxymethyl)pyridine

CAS 1206968-92-4: (5-bromo-3-fluoropyridin-2-yl)methanol

(5-Bromo-3-fluoropyridin-2-yl)methanol

Ref: IN-DA00347Z

5-Bromo-3-fluoro-2-(hydroxymethyl)pyridine

Ref: 54-PC52069

(5-Bromo-3-fluoropyridin-2-yl)methanol

Ref: 10-F461074

5-Bromo-3-fluoro-2-(hydroxymethyl)pyridine

Ref: 3D-GYB96892

(5-Bromo-3-fluoropyridin-2-yl)methanol

Ref: FT-G14978