CAS number | 870774-29-1 |
Molecular formula | C16H13BO2 |
Product name | 3-(naphthalene-2-yl)phenylboronic acid |
Molecular Structure |
Molecular Weight:248.08400
PSA:40.46000
LogP:2.18660
3-(Naphthalene-2-yl)phenylboronic acid is a boronic acid compound with a wide range of applications in organic synthesis, medicinal chemistry and nanotechnology. It is a white crystalline solid with a molecular formula of C13H10BNO2.
3-(Naphthalene-2-yl)phenylboronic acid is widely used as a reagent in organic synthesis and catalysis. It can be used as a catalyst in the synthesis of a variety of organic compounds, such as amines, esters, and amides. It can also be used as a ligand in the formation of metal complexes with transition metals, such as palladium, ruthenium, and nickel. Additionally, it is used in the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals.
In medicinal chemistry, 3-(Naphthalene-2-yl)phenylboronic acid is used as an intermediate for the synthesis of a range of drugs, particularly those that target cancer, inflammation, and cardiovascular diseases. It is also used as a ligand for the preparation of metal complexes for use as drug delivery agents.
In nanotechnology, 3-(Naphthalene-2-yl)phenylboronic acid is used in the preparation of nanomaterials, such as quantum dots and carbon nanotubes. It can be used as a linker molecule to attach a range of functional groups to nanomaterials, allowing for the production of nanomaterials with tailored properties and applications.
3-(Naphthalene-2-yl)phenylboronic acid is a versatile compound with a wide range of applications in organic synthesis, medicinal chemistry, and nanotechnology. It is available in a variety of forms, including powder, granules, and liquid solutions. It is stable in air and can be stored at room temperature for long periods of time. It is also soluble in common organic solvents such as dimethyl sulfoxide, dimethylformamide, and tetrahydrofuran.