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CAS 870718-03-9

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(3-bromo-2-butoxy-5-methylphenyl)boronic acid

Description:
(3-bromo-2-butoxy-5-methylphenyl)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, making it valuable in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a bromine atom and a butoxy group attached to a phenyl ring, which contributes to its hydrophobic characteristics and influences its reactivity. The presence of the boronic acid group allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as well as in materials science for creating boron-containing polymers. Its molecular structure suggests it may exhibit moderate solubility in organic solvents while being less soluble in water due to the hydrophobic butoxy group. Additionally, the compound's reactivity can be influenced by the electronic effects of the bromine and methyl substituents on the aromatic ring, which can affect its behavior in chemical reactions. Overall, this compound is of interest for its synthetic utility and potential applications in various fields of chemistry.
Formula:C11H16BBrO3
InChI:InChI=1/C11H16BBrO3/c1-3-4-5-16-11-9(12(14)15)6-8(2)7-10(11)13/h6-7,14-15H,3-5H2,1-2H3
SMILES:CCCCOc1c(cc(C)cc1Br)B(O)O
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