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CAS 36329-85-8

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Boronic acid,B-(3-phenylpropyl)-

Description:
Boronic acid, B-(3-phenylpropyl)-, with the CAS number 36329-85-8, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a 3-phenylpropyl 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. It is often employed in Suzuki coupling reactions, which are pivotal for constructing carbon-carbon bonds in the synthesis of complex organic molecules. The presence of the phenyl group contributes to its hydrophobic character, while the boronic acid functionality allows for interactions with biological molecules, potentially facilitating drug design and development. Additionally, boronic acids can act as pH-sensitive compounds, exhibiting changes in solubility and reactivity based on the pH of the environment. Overall, B-(3-phenylpropyl)-boronic acid is a versatile compound with significant utility in both synthetic and biological contexts.
Formula:C9H13BO2
Synonyms:
  • Boronicacid, (3-phenylpropyl)- (9CI)
  • (3-Phenylpropyl)boronic acid
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