CAS 128676-84-6
:2-Chloroquinoline-3-boronic acid
Description:
2-Chloroquinoline-3-boronic acid is an organic compound characterized by its boronic acid functional group and a chloro-substituted quinoline structure. It typically appears as a solid and is soluble in polar organic solvents. The presence of the boronic acid group allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, which are essential in the synthesis of biaryl compounds. The chloro group enhances its reactivity and can serve as a leaving group in nucleophilic substitution reactions. This compound is often utilized in medicinal chemistry and materials science due to its potential applications in drug development and organic synthesis. Additionally, it may exhibit biological activity, making it of interest in pharmaceutical research. Safety data should be consulted for handling, as boronic acids can be sensitive to moisture and may require specific storage conditions. Overall, 2-Chloroquinoline-3-boronic acid is a versatile building block in organic synthesis with significant implications in various chemical fields.
Formula:C9H7BClNO2
InChI:InChI=1/C9H7BClNO2/c11-9-7(10(13)14)5-6-3-1-2-4-8(6)12-9/h1-5,13-14H
SMILES:c1ccc2c(c1)cc(c(Cl)n2)B(O)O
Synonyms:- (2-Chloroquinolin-3-Yl)Boronic Acid
- 2-Chloroquinolin-3-boronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
Boronic acid, B-(2-chloro-3-quinolinyl)-
CAS:Formula:C9H7BClNO2Purity:95%Color and Shape:SolidMolecular weight:207.42142-Chloroquinoline-3-boronic acid
CAS:<p>2-Chloroquinoline-3-boronic acid</p>Purity:96%Color and Shape:SolidMolecular weight:207.42g/mol
