(2-Methyl-4-carboxyphenyl)boronic acid, with the CAS number 158429-66-4, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a carboxylic acid and a methyl substituent. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the carboxylic acid group. It exhibits properties typical of boronic acids, including the ability to form reversible complexes with diols, which makes it useful in various applications, including organic synthesis and medicinal chemistry. The carboxylic acid group contributes to its acidity and potential reactivity, while the methyl group can influence its steric and electronic properties. This compound is often utilized in the development of pharmaceuticals and as a building block in organic synthesis, particularly in the formation of carbon-carbon bonds through cross-coupling reactions. Its unique structure allows for specific interactions in biological systems, making it a subject of interest in drug design and development.

(2-METHYL-4-CARBOXYPHENYL)BORONIC ACID

158429-66-4: (2-Methyl-4-carboxyphenyl)boronic acid, with the CAS number 158429-66-4, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a carboxylic acid and a methyl substituent. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the carboxylic acid group. It exhibits properties typical of boronic acids, including the ability to form reversible complexes with diols, which makes it useful in various applications, including organic synthesis and medicinal chemistry. The carboxylic acid group contributes to its acidity and potential reactivity, while the methyl group can influence its steric and electronic properties. This compound is often utilized in the development of pharmaceuticals and as a building block in organic synthesis, particularly in the formation of carbon-carbon bonds through cross-coupling reactions. Its unique structure allows for specific interactions in biological systems, making it a subject of interest in drug design and development.

CAS 158429-66-4

(2-METHYL-4-CARBOXYPHENYL)BORONIC ACID

Benzoic acid, 4-borono-3-methyl-

Ref: IN-DA001Q6Z

(2-Methyl-4-carboxyphenyl)boronic acid

Ref: 54-OR360223

4-Borono-3-methylbenzoic acid

Ref: 10-F323798