CAS 745784-09-2
:B-(4-Chloro-3-quinolinyl)boronic acid
Description:
B-(4-Chloro-3-quinolinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a quinoline derivative. This compound typically exhibits a white to off-white solid appearance and is soluble in polar organic solvents, such as methanol and dimethyl sulfoxide, while being less soluble in non-polar solvents. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. The presence of the chloro substituent on the quinoline ring can influence its reactivity and biological activity, potentially enhancing its role as a pharmacophore in drug development. Additionally, B-(4-Chloro-3-quinolinyl)boronic acid may exhibit properties such as moderate stability under ambient conditions, but it should be handled with care due to the potential reactivity of boronic acids with moisture and other nucleophiles. Overall, this compound serves as an important building block in the synthesis of complex organic molecules.
Formula:C9H7BClNO2
InChI:InChI=1S/C9H7BClNO2/c11-9-6-3-1-2-4-8(6)12-5-7(9)10(13)14/h1-5,13-14H
InChI key:InChIKey=RCOYQAVBYWNJAL-UHFFFAOYSA-N
SMILES:ClC=1C2=C(N=CC1B(O)O)C=CC=C2
Synonyms:- (4-Chloroquinolin-3-yl)boronic acid
- Boronic acid, (4-chloro-3-quinolinyl)-
- B-(4-Chloro-3-quinolinyl)boronic acid
- (4-Chloroquinolin-3-yl)boronicacid
- Boronic acid, B-(4-chloro-3-quinolinyl)-
- (4-chloro-3-quinolinyl)-Boronic acid
- 4-Chloroquinoline-3-boronic acid, 97%
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