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CAS 871126-24-8

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{2-[(3-fluorobenzyl)oxy]phenyl}boronic acid

Description:
{2-[(3-fluorobenzyl)oxy]phenyl}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. This compound features a phenyl ring substituted with a 3-fluorobenzyl ether, enhancing its reactivity and potential applications in organic synthesis and medicinal chemistry. The fluorine atom introduces electronegativity, which can influence the compound's electronic properties and reactivity. Typically, boronic acids are utilized in Suzuki coupling reactions, making this compound valuable in the synthesis of complex organic molecules. Additionally, the presence of the boronic acid group allows for potential applications in drug development, particularly in targeting specific biological pathways. The compound is likely to be a white to off-white solid, soluble in polar organic solvents, and may exhibit moderate stability under standard laboratory conditions. As with many organoboron compounds, careful handling is advised due to potential reactivity and the need for specific storage conditions to maintain stability.
Formula:C13H12BFO3
InChI:InChI=1/C13H12BFO3/c15-11-5-3-4-10(8-11)9-18-13-7-2-1-6-12(13)14(16)17/h1-8,16-17H,9H2
SMILES:c1ccc(c(c1)B(O)O)OCc1cccc(c1)F
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