CAS 919347-69-6
:5-formylpyridin-3-ylboronic acid
Description:
5-Formylpyridin-3-ylboronic acid is an organic compound characterized by the presence of a pyridine ring substituted with both a formyl group and a boronic acid group. The molecular structure features a boron atom bonded to a hydroxyl group and an organic moiety, which in this case is a pyridine derivative. This compound typically exhibits properties such as being a solid at room temperature and is soluble in polar solvents like water and alcohols due to the presence of the boronic acid functional group. It is often utilized in organic synthesis, particularly in Suzuki coupling reactions, where it acts as a boron-containing reagent to form carbon-carbon bonds. The formyl group can also serve as a reactive site for further functionalization, making this compound valuable in medicinal chemistry and material science. Additionally, the presence of both the formyl and boronic acid functionalities allows for diverse reactivity, enabling the synthesis of various derivatives and complex molecules.
Formula:C6H6BNO3
InChI:InChI=1/C6H6BNO3/c9-4-5-1-6(7(10)11)3-8-2-5/h1-4,10-11H
SMILES:c1c(cncc1B(O)O)C=O
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
(5-formylpyridin-3-yl)boronic acid
CAS:Formula:C6H6BNO3Purity:>95%Color and Shape:SolidMolecular weight:150.92775-Formylpyridin-3-ylboronic acid
CAS:<p>5-Formylpyridin-3-ylboronic acid</p>Purity:≥95%Molecular weight:150.93g/mol

