Boronic acid, specifically the compound with the name "Boronic acid, B-[4-[[[(4-methoxyphenyl)methyl]amino]carbonyl]phenyl]-" and CAS number 874460-08-9, is characterized by its boron-containing functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a boronic acid moiety attached to a phenyl ring that is further substituted with a methoxy group and an amide functional group. The presence of the methoxy group enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, and can serve as important intermediates in the development of pharmaceuticals. Additionally, the specific structural features of this compound may impart unique properties, such as selective binding to certain biomolecules, making it of interest in medicinal chemistry and materials science. Overall, this compound exemplifies the diverse applications of boronic acids in various chemical and biological contexts.

Boronic acid,B-[4-[[[(4-methoxyphenyl)methyl]amino]carbonyl]phenyl]-

874460-08-9: Boronic acid, specifically the compound with the name "Boronic acid, B-[4-[[[(4-methoxyphenyl)methyl]amino]carbonyl]phenyl]-" and CAS number 874460-08-9, is characterized by its boron-containing functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a boronic acid moiety attached to a phenyl ring that is further substituted with a methoxy group and an amide functional group. The presence of the methoxy group enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, and can serve as important intermediates in the development of pharmaceuticals. Additionally, the specific structural features of this compound may impart unique properties, such as selective binding to certain biomolecules, making it of interest in medicinal chemistry and materials science. Overall, this compound exemplifies the diverse applications of boronic acids in various chemical and biological contexts.

(4-((4-Methoxybenzyl)carbamoyl)phenyl)boronic acid

<p>N-(4-Methoxybenzyl) 4-boronobenzamide</p>

CAS 874460-08-9

Boronic acid,B-[4-[[[(4-methoxyphenyl)methyl]amino]carbonyl]phenyl]-

(4-((4-Methoxybenzyl)carbamoyl)phenyl)boronic acid

Ref: IN-DA004HHX

N-(4-Methoxybenzyl) 4-boronobenzamide

Ref: 54-OR360442

(4-((4-Methoxybenzyl)carbamoyl)phenyl)boronic acid

Ref: 10-F217372