[2-(Bromomethyl)-4-fluoro-phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a bromomethyl group and a fluorophenyl moiety, contributing to its reactivity and potential for further functionalization. Typically, boronic acids exhibit moderate solubility in polar solvents and can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is valuable in the formation of carbon-carbon bonds. The presence of the bromine atom enhances its electrophilic character, while the fluorine atom can influence the electronic properties of the aromatic ring. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals, as well as in materials science for creating functionalized polymers and other advanced materials. Its specific reactivity and properties would depend on the surrounding conditions and the presence of other reactants.

[2-(bromomethyl)-4-fluoro-phenyl]boronic acid

850568-01-3: [2-(Bromomethyl)-4-fluoro-phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a bromomethyl group and a fluorophenyl moiety, contributing to its reactivity and potential for further functionalization. Typically, boronic acids exhibit moderate solubility in polar solvents and can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is valuable in the formation of carbon-carbon bonds. The presence of the bromine atom enhances its electrophilic character, while the fluorine atom can influence the electronic properties of the aromatic ring. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals, as well as in materials science for creating functionalized polymers and other advanced materials. Its specific reactivity and properties would depend on the surrounding conditions and the presence of other reactants.

(2-(Bromomethyl)-4-fluorophenyl)boronic acid

2-(Bromomethyl)-4-fluorobenzeneboronic acid

CAS 850568-01-3

[2-(bromomethyl)-4-fluoro-phenyl]boronic acid

(2-(Bromomethyl)-4-fluorophenyl)boronic acid

Ref: IN-DA004SIA

2-(Bromomethyl)-4-fluorobenzeneboronic acid

Ref: 54-PC1643

(2-(Bromomethyl)-4-fluorophenyl)boronic acid

Ref: 10-F218429