4-Chloro-2-methylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring. Its molecular structure features a phenyl ring substituted with a chlorine atom at the para position and a methyl group at the ortho position relative to the boronic acid group. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, which is a characteristic feature of boronic acids due to their ability to form hydrogen bonds. 4-Chloro-2-methylphenylboronic acid is often utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds. Additionally, it can serve as a reagent in the development of pharmaceuticals and agrochemicals. Its reactivity is influenced by the boronic acid moiety, allowing it to participate in various chemical transformations, including the formation of boronate esters. Proper handling and storage are essential due to its potential reactivity and the presence of chlorine, which may pose environmental and health risks.

4-Chloro-2-methylphenylboronic acid

209919-30-2: 4-Chloro-2-Methylbenzeneboronic Acid

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CAS 209919-30-2: 4-Chloro-2-methylphenylboronic acid

4-Chloro-2-methylphenylboronic acid

Ref: 3D-FC55459

4-Chloro-2-methylbenzeneboronic acid

Ref: 54-OR7181

4-Chloro-2-methylphenylboronic acid

Ref: 7W-GK6200

4-Chloro-2-methylphenylboronic acid

Ref: 10-F045268

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

Ref: 3B-C2577

4-Chloro-2-methylphenylboronic acid

Ref: IN-DA00362G