Boronic acid, specifically B-(6-bromo-5-methyl-3-pyridinyl)-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a pyridine ring that is substituted with a bromine atom and a methyl group. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid group, which can engage in hydrogen bonding. The bromine substituent can influence the compound's reactivity, making it useful in various chemical reactions, including Suzuki coupling, which is a method for forming carbon-carbon bonds. The methyl group can affect the electronic properties of the pyridine ring, potentially enhancing its nucleophilicity. Boronic acids are known for their ability to form reversible complexes with diols, which is a key feature in applications such as sensor technology and drug design. Overall, this compound is significant in organic synthesis and medicinal chemistry due to its versatile reactivity and functionalization potential.

Boronic acid,B-(6-bromo-5-methyl-3-pyridinyl)-

1003043-34-2: 2-Bromo-3-methylpyridine-5-boronicacid, 6-Bromo-5-methylpyridine-3-boronic acid, 2-Bromo-3-methylpyridine-5-boronic acid

6-Bromo-5-methylpyridine-3-boronic acid

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CAS 1003043-34-2: Boronic acid,B-(6-bromo-5-methyl-3-pyridinyl)-

6-Bromo-5-methylpyridine-3-boronic acid

Ref: 10-F210951

6-Bromo-5-methylpyridine-3-boronicacid

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6-Bromo-5-methylpyridine-3-boronic acid

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Boronic acid, B-(6-bromo-5-methyl-3-pyridinyl)-

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