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CAS 870717-99-0

:

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

Description:
(3-Bromo-2-methoxy-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. This compound features a phenyl ring substituted with a bromine atom, a methoxy group, and a methyl group, contributing to its unique reactivity and solubility properties. The presence of the boronic acid moiety allows it to participate in various chemical reactions, including Suzuki coupling, which is widely used in organic synthesis for forming carbon-carbon bonds. Additionally, the bromine substituent can serve as a leaving group in nucleophilic substitution reactions. The methoxy and methyl groups can influence the electronic properties of the molecule, potentially enhancing its reactivity or solubility in organic solvents. Overall, (3-bromo-2-methoxy-5-methylphenyl)boronic acid is a valuable compound in synthetic organic chemistry, particularly in the development of pharmaceuticals and advanced materials.
Formula:C8H10BBrO3
InChI:InChI=1/C8H10BBrO3/c1-5-3-6(9(11)12)8(13-2)7(10)4-5/h3-4,11-12H,1-2H3
SMILES:Cc1cc(c(c(c1)Br)OC)B(O)O
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