Boronic acid, specifically (2,4-dichloro-5-ethoxyphenyl)-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is substituted with both ethoxy and dichloro groups. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity in various chemical reactions, particularly in Suzuki coupling reactions, which are important in organic synthesis for forming carbon-carbon bonds. The presence of the ethoxy group enhances its solubility and reactivity, while the dichloro substituents can influence its electronic properties and steric hindrance. Boronic acids are known for their ability to form reversible complexes with diols, making them useful in applications such as drug delivery and sensor technology. Additionally, the specific arrangement of substituents in this compound can affect its biological activity and potential applications in medicinal chemistry. Overall, (2,4-dichloro-5-ethoxyphenyl)boronic acid is a versatile compound with significant implications in both synthetic and applied chemistry.

Boronic acid, (2,4-dichloro-5-ethoxyphenyl)-

915200-81-6: Boronic acid, specifically (2,4-dichloro-5-ethoxyphenyl)-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is substituted with both ethoxy and dichloro groups. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity in various chemical reactions, particularly in Suzuki coupling reactions, which are important in organic synthesis for forming carbon-carbon bonds. The presence of the ethoxy group enhances its solubility and reactivity, while the dichloro substituents can influence its electronic properties and steric hindrance. Boronic acids are known for their ability to form reversible complexes with diols, making them useful in applications such as drug delivery and sensor technology. Additionally, the specific arrangement of substituents in this compound can affect its biological activity and potential applications in medicinal chemistry. Overall, (2,4-dichloro-5-ethoxyphenyl)boronic acid is a versatile compound with significant implications in both synthetic and applied chemistry.

CAS 915200-81-6

Boronic acid, (2,4-dichloro-5-ethoxyphenyl)-

2,4-Dichloro-5-ethoxyphenylboronic acid

Ref: IN-DA00GTE8

2,4-Dichloro-5-ethoxyphenylboronic acid

Ref: 54-OR360391