CAS 395087-89-5

Boronic acid, 3-dibenzofuranyl-

Description:

Boronic acid, 3-dibenzofuranyl- (CAS 395087-89-5) is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a dibenzofuranyl moiety. 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 medicinal chemistry. The dibenzofuranyl group contributes to its aromatic character, potentially influencing its solubility and reactivity. Boronic acids are known for their role in Suzuki coupling reactions, which are vital for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the presence of the dibenzofuranyl structure may impart specific electronic and steric properties, affecting the compound's reactivity and interaction with biological targets. Overall, boronic acids like this one are valuable in both academic research and industrial applications due to their versatility and functionalization potential.

Formula: C₁₂H₉BO₃

dibenzo[b,d]furan-3-ylboronic acid

CAS: 395087-89-5

Formula: C₁₂H₉BO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 212.0091

Ref: IN-DA00CMCG

3-Dibenzofuranyl boronic acid

CAS: 395087-89-5

3-Dibenzofuranyl boronic acid

Purity: 99%

Molecular weight: 212.01g/mol

Ref: 54-OR55134

DIBENZO[B,D]FURAN-3-YLBORONIC ACID

CAS: 395087-89-5

Formula: C₁₂H₉BO₃

Purity: 97%

Molecular weight: 212.01

Ref: 10-F538570