5-Chloro-2-methylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, which is a common trait for boronic acids due to their ability to form hydrogen bonds. The presence of the chlorine atom and the methyl group on the phenyl ring influences its reactivity and solubility, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. The compound's reactivity, stability, and functionalization potential make it valuable in organic synthesis and materials science. Safety precautions should be taken when handling this substance, as with many organoboron compounds, due to potential toxicity and environmental concerns.

5-chloro-2-methylphenylboronic acid

148839-33-2: (5-Chloro-2-methylphenyl)boronic acid

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(5-Chloro-2-methylphenyl)boronic acid

5-Chloro-2-methylphenylboronic Acid (contains varying amounts of Anhydride)

CAS 148839-33-2: 5-chloro-2-methylphenylboronic acid

(5-Chloro-2-methylphenyl)boronic acid

Ref: 3D-FC139565

5-Chloro-2-methylphenylboronic Acid (contains varying amounts of Anhydride)

Ref: 3B-C2665

Boronic acid, B-(5-chloro-2-methylphenyl)-

Ref: IN-DA001L8R

5-Chloro-2-methylphenylboronic acid

Ref: 10-F093033

5-Chloro-2-methylbenzeneboronic acid

Ref: 54-OR10415

5-Chloro-2-methylphenylboronic acid

Ref: 7W-GK8242