CAS 877993-09-4

4-Phenylbiphenyl-4-ylboronic acid

Description:

4-Phenylbiphenyl-4-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a biphenyl structure with a phenyl substituent. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity due to the boronic acid group, which can participate in various chemical reactions, including Suzuki coupling, a widely used method for forming carbon-carbon bonds. The presence of the phenyl groups contributes to its stability and may influence its electronic properties, making it useful in organic synthesis and materials science. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. The compound's molecular structure and functional groups suggest potential applications in organic electronics, particularly in the development of organic semiconductors and light-emitting devices. Overall, 4-Phenylbiphenyl-4-ylboronic acid is a versatile compound with significant implications in both synthetic chemistry and material development.

Boronic acid, [1,1':4',1''-terphenyl]-4-yl-

CAS: 877993-09-4

Formula: C₁₈H₁₅BO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 274.1215

Ref: IN-DA00IERT

[1,1':4',1''-Terphenyl]-4-ylboronic acid

CAS: 877993-09-4

[1,1':4',1''-Terphenyl]-4-ylboronic acid

Purity: 97%

Molecular weight: 274.128g/mol

Ref: 54-OR74931

4-(4-BIPHENYL)PHENYL BORONIC ACID

CAS: 877993-09-4

Formula: C₁₈H₁₅BO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 274.13

Ref: 10-F466923