CAS 268218-94-6: [4-(phenylcarbonyl)phenyl]boronic acid

Description: [4-(Phenylcarbonyl)phenyl]boronic acid, with the CAS number 268218-94-6, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a phenylcarbonyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and materials science. The presence of the phenylcarbonyl moiety enhances its reactivity and solubility in organic solvents. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic chemistry. The compound's structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the ability of boronic acids to interact with biological targets. Overall, [4-(phenylcarbonyl)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

Formula: C₁₃H₁₁BO₃

InChI: InChI=1/C13H11BO3/c15-13(10-4-2-1-3-5-10)11-6-8-12(9-7-11)14(16)17/h1-9,16-17H

Synonyms:

• 4-Benzoylphenylboronic acid

4-BENZOYLBENZENEBORONIC ACID

CAS: 268218-94-6

• Formula: C₁₃H₁₁BO₃
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 226.0356

4-Benzoylbenzeneboronic acid

CAS: 268218-94-6

• Purity: 98%
• Molecular weight: 226.04g/mol

(4-Benzoylphenyl)boronic acid

CAS: 268218-94-6

• Purity: 95.0%
• Color and Shape: Solid
• Molecular weight: 226.0399932861328

4-Benzoylphenylboronic acid

CAS: 268218-94-6

4-Benzoylphenylboronic acid is a molecule that has been synthesised in the laboratory. It is a …

• Formula: C₁₃H₁₁BO₃
• Purity: Min. 95%
• Molecular weight: 226.04 g/mol