Boronic acid, (4-methoxy-3-pyridinyl)-, identified by CAS number 355004-67-0, is an organic compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols. The methoxy group enhances its solubility and reactivity, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. The pyridine ring contributes to its aromatic properties and can influence its electronic characteristics, making it a potential candidate for applications in pharmaceuticals and agrochemicals. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor technologies and drug delivery systems. Overall, this compound's unique structural features and reactivity profile make it a valuable substance in both research and industrial applications.

Boronic acid, (4-methoxy-3-pyridinyl)-

355004-67-0: (4-Methoxy-3-pyridinyl)-boronic acid, 4-Methoxypyridine-3-Boronic Acid, (4-Methoxypyridin-3-Yl)Boronic Acid

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CAS 355004-67-0: Boronic acid, (4-methoxy-3-pyridinyl)-

4-Methoxy-3-pyridineboronic acid hydrate, 97%

Ref: AC-37838

4-Methoxy-3-pyridineboronic acid

Ref: 10-F219361

4-Methoxypyridine-3-boronic acid

Ref: 54-OR7236

(4-Methoxypyridin-3-yl)boronic acid

Ref: IN-DA0032CX