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CAS 870718-02-8

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(3-bromo-5-methyl-2-propoxyphenyl)boronic acid

Description:
(3-bromo-5-methyl-2-propoxyphenyl)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 useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a bromine atom, a methyl group, and a propoxy group, contributing to its unique reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its reactivity can be influenced by the electronic and steric effects of the substituents on the phenyl ring. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and air, which can affect its stability and reactivity.
Formula:C10H14BBrO3
InChI:InChI=1/C10H14BBrO3/c1-3-4-15-10-8(11(13)14)5-7(2)6-9(10)12/h5-6,13-14H,3-4H2,1-2H3
SMILES:CCCOc1c(cc(C)cc1Br)B(O)O
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