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CAS 943153-22-8

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5-Chloro-2-methoxypyridine-3-boronic acid

Description:
5-Chloro-2-methoxypyridine-3-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 chemical reactions, particularly in Suzuki coupling reactions. This compound features a pyridine ring substituted with a chlorine atom and a methoxy group, contributing to its unique reactivity and solubility properties. The boronic acid moiety enhances its utility in organic synthesis, especially in the formation of carbon-carbon bonds. It is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. The presence of the chlorine atom can influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with other chemical species. Additionally, the methoxy group can provide steric hindrance and influence the compound's overall stability and reactivity. As with many boronic acids, it is important to handle this compound with care due to its potential reactivity and the need for proper storage conditions to maintain its integrity.
Formula:C6H7BClNO3
InChI:InChI=1/C6H7BClNO3/c1-12-6-5(7(10)11)2-4(8)3-9-6/h2-3,10-11H,1H3
SMILES:COc1c(cc(cn1)Cl)B(O)O
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