CAS 870774-29-1
:3-(2-Naphthyl)phenylboronic acid
Description:
3-(2-Naphthyl)phenylboronic acid 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 2-naphthyl group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with moderate solubility in polar organic solvents like methanol and ethanol, while being less soluble in non-polar solvents. The boronic acid group allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis, medicinal chemistry, and as a reagent in Suzuki coupling reactions. Additionally, the presence of the naphthyl moiety can enhance the compound's electronic properties and stability. Its unique structure contributes to its potential utility in drug development and materials science, particularly in the design of sensors and catalysts. As with many boronic acids, it is important to handle this compound with care, as it may have specific safety and environmental considerations.
Formula:C16H13BO2
Synonyms:- Boronic acid, [3-(2-naphthalenyl)phenyl]-
- 3-(Naphthalen-2-yl)phenylboronic acid
- 3-(2-Naphthyl)benzeneboronic acid
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Found 4 products.
3-(2-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride)
CAS:Formula:C16H13BO2Purity:97.0 to 108.0 %Color and Shape:White to Almost white powder to crystalMolecular weight:248.093-(Naphthalene-2-yl)phenylboronic acid
CAS:Formula:C16H13BO2Purity:98%Color and Shape:SolidMolecular weight:248.0842(3-(Naphthalen-2-yl)phenyl)boronic acid
CAS:(3-(Naphthalen-2-yl)phenyl)boronic acidPurity:98%Molecular weight:248.08g/mol



