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CAS 849052-24-0

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

Description:
{3-bromo-2-[(3-methoxybenzyl)oxy]phenyl}boronic acid, with the CAS number 849052-24-0, 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 methoxybenzyl ether moiety, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. The boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, the presence of the methoxy group can enhance solubility and influence the compound's electronic properties. Typically, boronic acids exhibit moderate stability under ambient conditions but can be sensitive to moisture and air, necessitating careful handling and storage. Overall, this compound's structural features suggest potential utility in drug development and materials science, particularly in the synthesis of complex organic molecules.
Formula:C14H14BBrO4
InChI:InChI=1/C14H14BBrO4/c1-19-11-5-2-4-10(8-11)9-20-14-12(15(17)18)6-3-7-13(14)16/h2-8,17-18H,9H2,1H3
SMILES:COc1cccc(c1)COc1c(cccc1Br)B(O)O
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