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CAS 836615-83-9

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{2,6-difluoro-3-[(2-fluorobenzyl)oxy]phenyl}boronic acid

Description:
{2,6-Difluoro-3-[(2-fluorobenzyl)oxy]phenyl}boronic acid is a boronic acid derivative characterized by its unique molecular structure, which includes a phenyl ring substituted with fluorine atoms and a boronic acid functional group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of fluorine atoms enhances its lipophilicity and can influence its biological activity. Additionally, the compound may exhibit moderate solubility in organic solvents and limited solubility in water, which is common for many boronic acids. Its reactivity can be leveraged in cross-coupling reactions, particularly in the synthesis of complex organic molecules. Overall, {2,6-difluoro-3-[(2-fluorobenzyl)oxy]phenyl}boronic acid is a valuable compound in the field of chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C13H10BF3O3
InChI:InChI=1/C13H10BF3O3/c15-9-4-2-1-3-8(9)7-20-11-6-5-10(16)12(13(11)17)14(18)19/h1-6,18-19H,7H2
SMILES:c1ccc(c(c1)COc1ccc(c(c1F)B(O)O)F)F
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