CAS 156635-87-9
:4-Benzyloxy-2,3-difluorobenzeneboronic acid
Description:
4-Benzyloxy-2,3-difluorobenzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in forming covalent bonds with various nucleophiles. This compound features a benzene ring substituted with both a benzyloxy group and two fluorine atoms, contributing to its unique electronic properties and potential applications in organic synthesis and medicinal chemistry. The difluorobenzene moiety enhances the compound's lipophilicity and may influence its biological activity. The boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the benzyloxy group can provide stability and solubility in organic solvents. Overall, 4-Benzyloxy-2,3-difluorobenzeneboronic acid is a versatile compound with significant implications in chemical research and development, particularly in the fields of pharmaceuticals and materials science.
Formula:BCoF4
InChI:InChI=1/BF4.Co/c2-1(3,4)5;/q-1;+2
SMILES:[B-](F)(F)(F)F.[Co]
Synonyms:- 4-Benzyloxy-2,3-difluorobenzeneboronic acid 98%
- 4-Benzyloxy-2,3-difluorobenzeneboronicacid98%
- Borate(1-), Tetrafluoro-, Cobalt(2+)
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Found 3 products.
Boronic acid, [2,3-difluoro-4-(phenylmethoxy)phenyl]- (9CI)
CAS:Formula:C13H11BF2O3Purity:97%Color and Shape:SolidMolecular weight:264.03244-Benzyloxy-2,3-difluorobenzeneboronic acid
CAS:<p>4-Benzyloxy-2,3-difluorobenzeneboronic acid</p>Formula:C13H11BF2O3Purity:98%Color and Shape: white solidMolecular weight:264.03g/mol4-Benzyloxy-2,3-difluorophenylboronic acid
CAS:Formula:C13H11BF2O3Purity:97%Color and Shape:SolidMolecular weight:264.03


