Boronic acid, specifically B-[4-[(ethoxymethyl)thio]phenyl]- (CAS 2096331-89-2), 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 an ethoxymethylthio group. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid moiety, which can engage in hydrogen bonding. The ethoxymethylthio substituent enhances its reactivity and may influence its interaction with biological molecules, making it of interest in medicinal chemistry and materials science. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is a key feature in applications such as drug design and sensor development. Additionally, the compound may exhibit unique electronic properties due to the conjugation between the boron atom and the aromatic system, potentially leading to interesting photophysical behavior. Overall, this compound's structure and functional groups contribute to its versatility in various chemical applications.

Boronic acid, B-[4-[(ethoxymethyl)thio]phenyl]-

2096331-89-2: Boronic acid, specifically B-[4-[(ethoxymethyl)thio]phenyl]- (CAS 2096331-89-2), 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 an ethoxymethylthio group. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid moiety, which can engage in hydrogen bonding. The ethoxymethylthio substituent enhances its reactivity and may influence its interaction with biological molecules, making it of interest in medicinal chemistry and materials science. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is a key feature in applications such as drug design and sensor development. Additionally, the compound may exhibit unique electronic properties due to the conjugation between the boron atom and the aromatic system, potentially leading to interesting photophysical behavior. Overall, this compound's structure and functional groups contribute to its versatility in various chemical applications.

CAS 2096331-89-2

Boronic acid, B-[4-[(ethoxymethyl)thio]phenyl]-

4-(Ethoxymethylthio)phenylboronic acid

Ref: IN-DA01EHDV

(4-((Ethoxymethyl)thio)phenyl)boronic acid

Ref: 54-OR1055332

4-(Ethoxymethylthio)phenylboronic acid

Ref: 10-F623552