
CAS 372521-91-0
:4-phenyl-1-naphthalene boronic acid
Description:
4-Phenyl-1-naphthalene boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring system, specifically at the 1-position, with a phenyl substituent at the 4-position. This compound typically exhibits properties such as being a white to off-white solid, and it is soluble in polar organic solvents like methanol and ethanol, but 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 and as a building block in the development of pharmaceuticals and materials science. Additionally, it can participate in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic molecules. The compound's structure contributes to its potential in sensor technology and drug delivery systems, where selective binding and release mechanisms are crucial. Overall, 4-phenyl-1-naphthalene boronic acid is a versatile compound with significant implications in both research and industrial applications.
- 4-Phenyl(naphthalene-1-yl)boronic acid
- 4-Phenylnaphthalene-1-boronic Acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
4-Phenylnaphthalene-1-boronic Acid (contains varying amounts of Anhydride)
CAS:Formula:C16H13BO2Purity:min. 98.0 area%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:248.094-PHENYLNAPHTHALEN-1-YLBORONIC ACID
CAS:Formula:C16H13BO2Purity:97%Color and Shape:SolidMolecular weight:248.08424-Phenylnaphthalene-1-boronic acid
CAS:4-Phenylnaphthalene-1-boronic acidPurity:98%Molecular weight:248.08g/mol(4-Phenylnaphthalen-1-yl)boronic acid
CAS:Formula:C16H13BO2Purity:98%Color and Shape:SolidMolecular weight:248.09



