L15193 3-(Hydroxymethyl)benzeneboronic acid, 98%
SDS
3-(Hydroxymethyl)benzeneboronic acid, 98%
Chemical Properties
Applications
Reactant used for copper-mediated trifluoromethylation, copper-catalyzed transformations from arylboronic acids in water, Mitsunobu, Suzuki, and amidation reactions with hydroxyphenylamino bromopyrazinecarboxylate. Reactant involved in the synthesis of biologically active molecules including Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors via Suzuki coupling reactions, HIV protease inhibitors with antiviral activity against drug-resistant viruses, Pyrrole derivatives for use as PDE4B inhibitors.
Notes
Literature References
Cheng-Pan Zhang et. al. Copper-mediated trifluoromethylation of arylboronic acids by trifluoromethyl sulfonium salts.. ChemicalCommunications.2011, 47,(33), 9516-9518.
Haijun Yang et. al. General copper-catalyzed transformations of functional groups from arylboronic acids in water. Chemistry: A European Journal.2011, 17, (20), 5652-5660.
GHS Hazard and Precautionary Statements
Hazard Statements: H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Precautionary Statements: P261-P280a-P305+P351+P338-P304+P340-P405-P501a
Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.
