(3-Bromo-2-fluoro-5-methyl-phenyl)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 bromine, fluorine, and a methyl group. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of the bromine and fluorine substituents can influence its reactivity and interactions, making it useful in various chemical applications, including cross-coupling reactions in organic synthesis. Boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor technology and drug delivery systems. Additionally, the specific arrangement of substituents on the phenyl ring can affect the compound's electronic properties and steric hindrance, impacting its reactivity in chemical reactions. Overall, (3-bromo-2-fluoro-5-methyl-phenyl)boronic acid is a versatile compound with significant utility in synthetic organic chemistry.

(3-bromo-2-fluoro-5-methyl-phenyl)boronic acid

957066-00-1: (3-Bromo-2-fluoro-5-methyl-phenyl)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 bromine, fluorine, and a methyl group. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of the bromine and fluorine substituents can influence its reactivity and interactions, making it useful in various chemical applications, including cross-coupling reactions in organic synthesis. Boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor technology and drug delivery systems. Additionally, the specific arrangement of substituents on the phenyl ring can affect the compound's electronic properties and steric hindrance, impacting its reactivity in chemical reactions. Overall, (3-bromo-2-fluoro-5-methyl-phenyl)boronic acid is a versatile compound with significant utility in synthetic organic chemistry.

CAS 957066-00-1

(3-bromo-2-fluoro-5-methyl-phenyl)boronic acid

Boronic acid,B-(3-bromo-2-fluoro-5-methylphenyl)-

Ref: IN-DA00IJDS

3-Borono-5-bromo-4-fluorotoluene

Ref: 54-PC412116

(3-Bromo-2-fluoro-5-methylphenyl)boronic acid

Ref: 10-F216254