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CAS 918655-03-5

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[4-(2-Naphthyl)phenyl]boronic acid

Description:
[4-(2-Naphthyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a biphenyl structure. This compound features a phenyl ring substituted with a 2-naphthyl group, which contributes to its unique properties. It is typically a white to off-white solid that is soluble in organic solvents such as ethanol and dimethyl sulfoxide, but less soluble in water. The boronic acid moiety allows for reversible covalent bonding with diols, making it useful in various applications, including organic synthesis, medicinal chemistry, and materials science. Its ability to form complexes with carbohydrates and other biomolecules is particularly significant in the development of sensors and drug delivery systems. Additionally, [4-(2-Naphthyl)phenyl]boronic acid can participate in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic molecules. Overall, this compound is valued for its versatility in chemical reactions and potential applications in pharmaceuticals and materials development.
Formula:C16H13BO2
InChI:InChI=1/C16H13BO2/c18-17(19)16-9-7-13(8-10-16)15-6-5-12-3-1-2-4-14(12)11-15/h1-11,18-19H
SMILES:c1ccc2cc(ccc2c1)c1ccc(cc1)B(O)O
Synonyms:
  • boronic acid, B-[4-(2-naphthalenyl)phenyl]-
  • 4-(2-Naphthyl)Phenylboronic Acid
  • 4-(Naphthalen-2-yl)Phenylboronic acid
  • 4-(Naphthalene-2-Yl)Phenylboronic Acid
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