3-Methoxy-4-(trifluoromethoxy)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with both a methoxy group and a trifluoromethoxy group, which can influence its electronic properties and reactivity. The trifluoromethoxy group is particularly notable for its strong electron-withdrawing effects, which can enhance the acidity of the boronic acid moiety. The presence of the methoxy group can also affect solubility and reactivity. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the unique substituents may impart specific biological activities or enhance the compound's utility in pharmaceutical applications. Overall, 3-Methoxy-4-(trifluoromethoxy)phenylboronic acid is a versatile compound with significant potential in both synthetic and medicinal chemistry.

3-Mthoxy-4-(trifluoromethoxy)phenylboronic acid

2096329-73-4: 3-Methoxy-4-(trifluoromethoxy)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with both a methoxy group and a trifluoromethoxy group, which can influence its electronic properties and reactivity. The trifluoromethoxy group is particularly notable for its strong electron-withdrawing effects, which can enhance the acidity of the boronic acid moiety. The presence of the methoxy group can also affect solubility and reactivity. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the unique substituents may impart specific biological activities or enhance the compound's utility in pharmaceutical applications. Overall, 3-Methoxy-4-(trifluoromethoxy)phenylboronic acid is a versatile compound with significant potential in both synthetic and medicinal chemistry.

CAS 2096329-73-4

3-Mthoxy-4-(trifluoromethoxy)phenylboronic acid

3-Methoxy-4-(trifluoromethoxy)phenylboronic acid

Ref: IN-DA01EHHU

3-Methoxy-4-(trifluoromethoxy)phenylboronic acid

Ref: 54-PC901713

(3-Methoxy-4-(trifluoromethoxy)phenyl)boronic acid

Ref: 10-F694291