Boronic acid, specifically the compound with the name "Boronic acid, B-[3-[[4-(heptyloxy)phenoxy]methyl]phenyl]-" and CAS number 870778-93-1, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with a heptyloxyphenyl moiety. This structure imparts unique properties, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis, drug development, and materials science. The heptyloxy group enhances the compound's solubility in organic solvents and may influence its biological activity. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic chemistry. Additionally, the presence of the boron atom allows for potential applications in sensors and as intermediates in the synthesis of complex organic molecules. Overall, this compound exemplifies the versatility and utility of boronic acids in both academic research and industrial applications.

Boronic acid,B-[3-[[4-(heptyloxy)phenoxy]methyl]phenyl]-

870778-93-1: Boronic acid, specifically the compound with the name "Boronic acid, B-[3-[[4-(heptyloxy)phenoxy]methyl]phenyl]-" and CAS number 870778-93-1, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with a heptyloxyphenyl moiety. This structure imparts unique properties, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis, drug development, and materials science. The heptyloxy group enhances the compound's solubility in organic solvents and may influence its biological activity. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic chemistry. Additionally, the presence of the boron atom allows for potential applications in sensors and as intermediates in the synthesis of complex organic molecules. Overall, this compound exemplifies the versatility and utility of boronic acids in both academic research and industrial applications.

CAS 870778-93-1

Boronic acid,B-[3-[[4-(heptyloxy)phenoxy]methyl]phenyl]-

3-(4'-Heptyloxyphenoxymethyl)phenylboronic acid

Ref: IN-DA003BQ0

3-(4'-Heptyloxyphenoxymethyl)phenylboronic acid

Ref: 54-OR360425