{4-[(Trifluoroethenyl)oxy]phenyl}boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a trifluoroethenyl ether. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications including organic synthesis and materials science. The trifluoroethenyl group introduces significant electron-withdrawing characteristics, which can influence the reactivity and stability of the compound. Additionally, the presence of fluorine atoms often enhances lipophilicity and can affect the compound's solubility in organic solvents. The compound may also exhibit interesting optical properties due to the conjugated system formed by the phenyl and trifluoroethenyl moieties. Overall, {4-[(trifluoroethenyl)oxy]phenyl}boronic acid is a versatile compound with potential applications in medicinal chemistry, particularly in the development of pharmaceuticals and agrochemicals.

{4-[(trifluoroethenyl)oxy]phenyl}boronic acid

213701-14-5: {4-[(Trifluorovinyl)oxy]phenyl}boronic acid, Boronic acid, B-[4-[(1,2,2-trifluoroethenyl)oxy]phenyl]-

CAS 213701-14-5: {4-[(trifluoroethenyl)oxy]phenyl}boronic acid

4-(Trifluorovinyloxyphenyl)boronic acid

Ref: 10-F023228

4-(Trifluorovinyloxyphenyl)boronic acid

Ref: IN-DA00C17L