Boronic acid, specifically B-(2,3-difluoro-4-propylphenyl)-, is an organoboron compound characterized by the presence of a boron atom bonded to a phenyl group that is substituted with fluorine and a propyl group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and materials science. The presence of fluorine atoms can enhance the compound's lipophilicity and influence its reactivity and stability. Additionally, the propyl group contributes to the hydrophobic character of the molecule. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic chemistry. The specific structural features of B-(2,3-difluoro-4-propylphenyl)- may also impart unique electronic properties, potentially making it suitable for applications in pharmaceuticals or agrochemicals. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry.

Boronic acid,B-(2,3-difluoro-4-propylphenyl)-

844699-71-4: Boronic acid, specifically B-(2,3-difluoro-4-propylphenyl)-, is an organoboron compound characterized by the presence of a boron atom bonded to a phenyl group that is substituted with fluorine and a propyl group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and materials science. The presence of fluorine atoms can enhance the compound's lipophilicity and influence its reactivity and stability. Additionally, the propyl group contributes to the hydrophobic character of the molecule. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic chemistry. The specific structural features of B-(2,3-difluoro-4-propylphenyl)- may also impart unique electronic properties, potentially making it suitable for applications in pharmaceuticals or agrochemicals. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry.

CAS 844699-71-4

Boronic acid,B-(2,3-difluoro-4-propylphenyl)-

Boronic acid,B-(2,3-difluoro-4-propylphenyl)-

Ref: IN-DA008I24