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CAS 256383-45-6

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B-(4-Nonylphenyl)boronic acid

Description:
B-(4-Nonylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a nonylphenyl moiety. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents, such as ethanol and dichloromethane, while being less soluble in water due to its hydrophobic nonylphenyl group. It is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds in the development of pharmaceuticals and advanced materials. The boronic acid group allows for reversible binding with diols, making it useful in sensor applications and in the development of boron-based materials. Additionally, B-(4-Nonylphenyl)boronic acid may exhibit biological activity, necessitating careful handling and consideration of its environmental impact. As with many organoboron compounds, it is important to follow safety guidelines during its use and disposal.
Formula:C15H25BO2
InChI:InChI=1S/C15H25BO2/c1-2-3-4-5-6-7-8-9-14-10-12-15(13-11-14)16(17)18/h10-13,17-18H,2-9H2,1H3
InChI key:InChIKey=VONVJOGSLHAKOX-UHFFFAOYSA-N
SMILES:C(CCCCCCCC)C1=CC=C(B(O)O)C=C1
Synonyms:
  • (4-Nonylphenyl)Boronic Acid
  • 4-N-Nonylphenylboronicacid
  • 4-Nonylphenylboronic acid
  • 4-Nonylphenylboronicacid
  • B-(4-Nonylphenyl)boronic acid
  • Boronic acid, (4-nonylphenyl)-
  • Boronic acid, B-(4-nonylphenyl)-
  • p-Nonylphenylboronic acid
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