B-(2-Chloro-3-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated aromatic ring. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. The presence of the chloro and methyl substituents on the phenyl ring can influence its reactivity and interactions, making it useful in various chemical applications, 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 is significant in biological and medicinal chemistry contexts. The compound's unique structure allows it to participate in diverse chemical transformations, making it valuable in organic synthesis and material science. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential toxicity and reactivity.

B-(2-Chloro-3-methylphenyl)boronic acid

915070-53-0: Boronic acid, (2-chloro-3-methylphenyl)-, Boronic acid, B-(2-chloro-3-methylphenyl)-, 2-Chloro-3-methylphenylboronic acid, B-(2-Chloro-3-methylphenyl)boronic acid

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CAS 915070-53-0: B-(2-Chloro-3-methylphenyl)boronic acid

2-Chloro-3-methylphenylboronic acid

Ref: 3D-FC160965

(2-Chloro-3-methylphenyl)boronic acid

Ref: 10-F216083

2-Chloro-3-methylphenylboronic acid

Ref: 54-OR360967

2-CHLORO-3-METHYLPHENYLBORONIC ACID

Ref: IN-DA00GTDH