(2,6-Difluoro-4-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with two fluorine atoms and a methoxy group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with moderate solubility in polar solvents like water and alcohols due to the boronic acid moiety. The presence of fluorine atoms enhances its electronic properties, making it useful in various applications, including medicinal chemistry and materials science. The methoxy group can influence the compound's reactivity and solubility, while the boronic acid functionality allows for participation in Suzuki coupling reactions, which are valuable in organic synthesis. Additionally, this compound may exhibit unique biological activities, making it a subject of interest in pharmaceutical research. Proper handling and storage are essential, as boronic acids can be sensitive to moisture and air, which may affect their stability and reactivity.

(2,6-difluoro-4-methoxyphenyl)boronic acid

406482-20-0: 2,6-Difluoro-4-methoxyphenylboronic acid

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(2,6-difluoro-4-methoxyphenyl)boronic Acid

2,6-Difluoro-4-methoxyphenylboronic acid

2,6-Difluoro-4-methoxybenzeneboronic acid

CAS 406482-20-0: (2,6-difluoro-4-methoxyphenyl)boronic acid

(2,6-difluoro-4-methoxyphenyl)boronic Acid

Ref: 3D-FD105122

2,6-Difluoro-4-methoxyphenylboronic acid

Ref: 10-F078459

2,6-Difluoro-4-methoxybenzeneboronic acid

Ref: 54-PC3437

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

Ref: 3B-D4728

Boronic acid, (2,6-difluoro-4-methoxyphenyl)-

Ref: IN-DA00I7Z4