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CAS 870777-28-9

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{3-chloro-4-[(2-fluorobenzyl)oxy]phenyl}boronic acid

Description:
{3-chloro-4-[(2-fluorobenzyl)oxy]phenyl}boronic acid, with the CAS number 870777-28-9, 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 chlorophenyl moiety and a fluorobenzyl ether, contributing to its unique reactivity and potential applications in medicinal chemistry and organic synthesis. The presence of the chlorine and fluorine substituents can influence the electronic properties and steric hindrance of the molecule, affecting its interactions in biological systems. Boronic acids are often utilized in Suzuki coupling reactions, making this compound potentially valuable in the synthesis of complex organic molecules. Additionally, the solubility and stability of this compound in various solvents can vary, which is important for its practical applications. Overall, {3-chloro-4-[(2-fluorobenzyl)oxy]phenyl}boronic acid is a versatile compound with significant implications in chemical research and development.
Formula:C13H11BClFO3
InChI:InChI=1/C13H11BClFO3/c15-11-7-10(14(17)18)5-6-13(11)19-8-9-3-1-2-4-12(9)16/h1-7,17-18H,8H2
SMILES:c1ccc(c(c1)COc1ccc(cc1Cl)B(O)O)F
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