Boronic acid, specifically 3-(methoxymethoxy)phenyl boronic acid, is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a methoxymethoxy group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and possessing moderate stability under standard conditions. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. Its unique structure enables it to participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the methoxymethoxy substituent can influence the compound's reactivity and solubility, enhancing its utility in drug development and material science. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their role in developing complex molecular architectures.

Boronic acid,[3-(methoxymethoxy)phenyl]- (9CI)

216443-40-2: Boronic acid, specifically 3-(methoxymethoxy)phenyl boronic acid, is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a methoxymethoxy group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and possessing moderate stability under standard conditions. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. Its unique structure enables it to participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the methoxymethoxy substituent can influence the compound's reactivity and solubility, enhancing its utility in drug development and material science. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their role in developing complex molecular architectures.

CAS 216443-40-2

Boronic acid,[3-(methoxymethoxy)phenyl]- (9CI)

(3-(Methoxymethoxy)phenyl)boronic acid

Ref: IN-DA007PO0

3-(Methoxymethoxy)phenylboronic acid

Ref: 54-OR360231

(3-(Methoxymethoxy)phenyl)boronic acid

Ref: 10-F219075