2,4,6-Trichlorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with three chlorine atoms at the 2, 4, and 6 positions. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. It exhibits properties typical of boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of chlorine substituents enhances its reactivity and can influence its electronic properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, 2,4,6-trichlorophenylboronic acid can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a widely used method for forming carbon-carbon bonds in organic synthesis. Safety precautions should be taken when handling this compound, as boronic acids can be irritants and may pose environmental hazards.

2,4,6-Trichlorophenylboronic acid

73852-18-3: 2,4,6-Trichlorobenzeneboronic acid

CAS 73852-18-3: 2,4,6-Trichlorophenylboronic acid

2,4,6-Trichlorobenzeneboronic acid

Ref: 54-OR3330

2,4,6-Trichlorophenylboronic Acid (contains varying amounts of Anhydride)

Ref: 3B-T3382

2,4,6-Trichlorophenylboronic acid

Ref: IN-DA005W7D

2,4,6-Trichlorophenylboronic acid

Ref: 10-F319120