2-Quinolinyl-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a quinoline ring system. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents like methanol and dimethyl sulfoxide, but generally insoluble in non-polar solvents. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. It can participate in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic molecules. Additionally, the quinoline structure contributes to its potential biological activity, as quinoline derivatives are known for their diverse pharmacological properties. The compound's reactivity and functional versatility make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety data should be consulted for handling and storage, as boronic acids can be sensitive to moisture and may require specific precautions.

2-quinolinyl-boronic acid

745784-12-7: 2-Quinolinyl-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a quinoline ring system. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents like methanol and dimethyl sulfoxide, but generally insoluble in non-polar solvents. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. It can participate in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic molecules. Additionally, the quinoline structure contributes to its potential biological activity, as quinoline derivatives are known for their diverse pharmacological properties. The compound's reactivity and functional versatility make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety data should be consulted for handling and storage, as boronic acids can be sensitive to moisture and may require specific precautions.

CAS 745784-12-7

2-quinolinyl-boronic acid

quinolin-2-ylboronic acid

Ref: IN-DA003U3H

Quinoline-2-boronic acid

Ref: 7W-GK1614

Quinoline-2-boronic acid

Ref: 54-OR8861

Quinolin-2-ylboronic acid

Ref: 10-F694135