CymitQuimica logo

CAS 2096333-80-9

:

B-(3-Chloro-8-isoquinolinyl)boronic acid

Description:
B-(3-Chloro-8-isoquinolinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a chloro-substituted isoquinoline moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the chloro group can influence its reactivity and solubility, while the isoquinoline structure may contribute to its biological activity. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Additionally, this compound may exhibit unique properties such as fluorescence or specific binding affinities, depending on its structural features. Its potential applications could extend to drug development, particularly in targeting specific biological pathways or as a building block in the synthesis of more complex molecules. As with all chemical substances, safety and handling precautions should be observed due to potential hazards associated with its components.
Formula:C9H7BClNO2
InChI:InChI=1S/C9H7BClNO2/c11-9-4-6-2-1-3-8(10(13)14)7(6)5-12-9/h1-5,13-14H
InChI key:InChIKey=BGXXCAYEDUMSSL-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C2=C(C=C(Cl)N=C2)C=CC1
Synonyms:
  • Boronic acid, B-(3-chloro-8-isoquinolinyl)-
  • B-(3-Chloro-8-isoquinolinyl)boronic acid
  • 3-Chloroisoquinoline-8-boronic acid
  • (3-Chloroisoquinolin-8-yl)boronic acid
  • 8-Borono-3-chloroisoquinoline, 8-Borono-3-chloro-2-azanaphthalene
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.