(3-Fluoro-5-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has both a fluorine atom and a methyl group as substituents. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. Its structure allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. The presence of the boronic acid group makes it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, the fluorine atom can enhance the compound's biological activity and lipophilicity, while the methyl group may influence its steric properties. As with many boronic acids, it is important to handle this compound with care, as it can be sensitive to moisture and may require specific storage conditions to maintain stability. Overall, (3-fluoro-5-methylphenyl)boronic acid is a versatile building block in modern organic chemistry.

(3-fluoro-5-methylphenyl)boronic acid

850593-06-5: boronic acid, B-(3-fluoro-5-methylphenyl)-, 3-Fluoro-5-Methylbenzeneboronic Acid

(3-Fluoro-5-methylphenyl)boronic acid

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CAS 850593-06-5: (3-fluoro-5-methylphenyl)boronic acid

(3-Fluoro-5-methylphenyl)boronic acid

Ref: 10-F092397

(3-fluoro-5-methylphenyl)boronic Acid

Ref: 3D-FF104619

(3-Fluoro-5-methylphenyl)boronic acid

Ref: IN-DA004YHJ

3-Fluoro-5-methylbenzeneboronic acid

Ref: 54-PC1610

3-Fluoro-5-methylphenylboronic Acid (contains varying amounts of Anhydride)

Ref: 3B-F1068