Boronic acid, specifically (3-ethoxy-4-methoxyphenyl)-, is an organic compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with ethoxy and methoxy groups. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar solvents like water and alcohols, due to the presence of the boronic acid moiety. The ethoxy and methoxy substituents enhance its lipophilicity and can influence its reactivity, particularly in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. Boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. Additionally, the presence of the boron atom contributes to unique electronic properties, which can be exploited in the design of sensors and catalysts. Overall, this compound is significant in both synthetic organic chemistry and medicinal chemistry.

Boronic acid, (3-ethoxy-4-methoxyphenyl)-

915201-13-7: Boronic acid, specifically (3-ethoxy-4-methoxyphenyl)-, is an organic compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with ethoxy and methoxy groups. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar solvents like water and alcohols, due to the presence of the boronic acid moiety. The ethoxy and methoxy substituents enhance its lipophilicity and can influence its reactivity, particularly in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. Boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. Additionally, the presence of the boron atom contributes to unique electronic properties, which can be exploited in the design of sensors and catalysts. Overall, this compound is significant in both synthetic organic chemistry and medicinal chemistry.

3-Ethoxy-4-methoxyphenylboronic acid

<p>3-Ethoxy-4-methoxyphenylboronic acid</p>

CAS 915201-13-7

Boronic acid, (3-ethoxy-4-methoxyphenyl)-

3-Ethoxy-4-methoxyphenylboronic acid

Ref: IN-DA00H1UV

3-Ethoxy-4-methoxyphenylboronic acid

Ref: 54-OR361199

(3-Ethoxy-4-methoxyphenyl)boronic acid

Ref: 10-F210285