CAS 943836-24-6

4-(Dibiphenyl-4-yl amino)phenylboronic acid

Description:

4-(Dibiphenyl-4-yl amino)phenylboronic acid, identified by its CAS number 943836-24-6, is an organic compound that features a boronic acid functional group, which is characterized by the presence of a boron atom bonded to a hydroxyl group and an aryl group. This compound typically exhibits properties associated with both boronic acids and amines, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as drug development and materials science. The presence of the dibiphenyl group enhances its electronic properties and solubility in organic solvents. Additionally, the compound may exhibit fluorescence, which can be advantageous for applications in sensing and imaging. Its structural characteristics suggest potential reactivity in cross-coupling reactions, commonly utilized in organic synthesis. Overall, 4-(Dibiphenyl-4-yl amino)phenylboronic acid is a versatile compound with significant implications in both academic research and industrial applications.

Synonyms:

• b-(4-(bis((1,1'-biphenyl)-4-yl)amino)phenyl)-boronic acid

(4-(Di([1,1'-biphenyl]-4-yl)amino)phenyl)boronicacid

CAS: 943836-24-6

Formula: C₃₀H₂₄BNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 441.3281

Ref: IN-DA00II4D

(4-(Di([1,1'-biphenyl]-4-yl)amino)phenyl)boronic acid

CAS: 943836-24-6

(4-(Di([1,1'-biphenyl]-4-yl)amino)phenyl)boronic acid

Purity: 97%

Ref: 54-OR1039263

(4-(Di([1,1′-biphenyl]-4-yl)amino)phenyl)boronic acid

CAS: 943836-24-6

Purity: 97%

Molecular weight: 441.3399963

Ref: 10-F762950