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CAS 870778-86-2

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

Description:
{3-bromo-2-[(2-fluorobenzyl)oxy]phenyl}boronic acid, with the CAS number 870778-86-2, 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 bromine atom and a fluorobenzyl ether moiety, contributing to its unique reactivity and potential applications in medicinal chemistry and organic synthesis. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, the fluorine atom can enhance the compound's lipophilicity and influence its biological activity. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structural characteristics suggest potential applications in drug development, particularly in the design of inhibitors or other biologically active molecules. As with many organoboron compounds, careful handling and storage are recommended due to their sensitivity to moisture and air.
Formula:C13H11BBrFO3
InChI:InChI=1/C13H11BBrFO3/c15-11-6-3-5-10(14(17)18)13(11)19-8-9-4-1-2-7-12(9)16/h1-7,17-18H,8H2
SMILES:c1ccc(c(c1)COc1c(cccc1Br)B(O)O)F
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