CAS 849062-09-5
:(2,6-difluoro-3-formylphenyl)boronic acid
Description:
(2,6-Difluoro-3-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with two fluorine atoms at the 2 and 6 positions and an aldehyde group at the 3 position, contributing to its reactivity and potential for further functionalization. The presence of fluorine atoms can enhance the compound's lipophilicity and influence its electronic properties, which may affect its interactions in biological systems. Additionally, boronic acids are often utilized in Suzuki coupling reactions, allowing for the formation of carbon-carbon bonds, which is a valuable tool in the synthesis of complex organic molecules. Overall, (2,6-difluoro-3-formylphenyl)boronic acid exhibits unique chemical properties that make it a significant compound in both research and industrial applications.
Formula:C7H5BF2O3
InChI:InChI=1/C7H5BF2O3/c9-5-2-1-4(3-11)7(10)6(5)8(12)13/h1-3,12-13H
SMILES:c1cc(c(c(c1C=O)F)B(O)O)F
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Found 3 products.
2,6-Difluoro-3-formylphenylboronic acid
CAS:Formula:C7H5BF2O3Purity:98%Color and Shape:SolidMolecular weight:185.92062,6-Difluoro-3-formylphenylboronic acid
CAS:<p>2,6-Difluoro-3-formylphenylboronic acid</p>Purity:≥95%Molecular weight:185.92g/mol
