CAS 190788-62-6
:QUINOLINE-8-BORONIC ACID, PINACOL ESTER
Description:
Quinoline-8-boronic acid, pinacol ester, is an organoboron compound characterized by the presence of a quinoline moiety and a boronic acid functional group that is protected as a pinacol ester. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as dichloromethane and ethanol. It is often utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its ability to act as a boron source. The pinacol ester protection enhances its stability and solubility, making it easier to handle in various chemical reactions. Additionally, quinoline derivatives are known for their biological activity, which may extend to this compound, although specific biological properties would require further investigation. Safety data indicates that, like many organoboron compounds, it should be handled with care, as it may pose risks if ingested or inhaled. Overall, quinoline-8-boronic acid, pinacol ester, is a valuable intermediate in synthetic organic chemistry with potential applications in pharmaceuticals and materials science.
Formula:C15H20BNO3
Synonyms:- QUINOLINE-8-BORONIC ACID,PINACOL ESTER
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Found 3 products.
Quinoline-8-boronic acid pinacol ester, 95%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C15H18BNO2Purity:95%Molecular weight:255.128-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl);quinoline
CAS:Formula:C15H18BNO2Purity:95%Molecular weight:255.11998-Quinolineboronic acid pinacol ester
CAS:<p>8-Quinolineboronic acid pinacol ester</p>Molecular weight:255.12g/mol


