B-(3-Methyl-5-propoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a propoxy group and a methyl group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the propoxy and methyl substituents can influence its solubility, reactivity, and overall stability. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic synthesis. Additionally, the specific arrangement of substituents in B-(3-Methyl-5-propoxyphenyl)boronic acid may impart unique electronic and steric properties, affecting its reactivity and interaction with biological targets. Overall, this compound is of interest in both synthetic chemistry and potential pharmaceutical applications due to its versatile reactivity and functional group characteristics.

B-(3-Methyl-5-propoxyphenyl)boronic acid

1256346-06-1: B-(3-Methyl-5-propoxyphenyl)boronic acid, Boronic acid, B-(3-methyl-5-propoxyphenyl)-

CAS 1256346-06-1: B-(3-Methyl-5-propoxyphenyl)boronic acid

3-Methyl-5-propoxyphenylboronic acid

Ref: 54-OR361465

3-Methyl-5-propoxyphenylboronic acid

Ref: 3D-GAC34606

(3-Methyl-5-propoxyphenyl)boronic acid

Ref: 10-F228591

Boronic acid, B-(3-methyl-5-propoxyphenyl)-

Ref: IN-DA000O1N