Boronic acid, specifically 2-(phenylmethoxy)-5-(trifluoromethyl)phenyl boronic acid, 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 phenylmethoxy group and a trifluoromethyl group. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The trifluoromethyl group enhances its electronic properties, potentially increasing its lipophilicity and influencing its biological activity. Boronic acids are known for their ability to form reversible complexes with diols, which is a key feature in applications such as drug design and sensor development. Additionally, the presence of the phenylmethoxy group may contribute to the compound's stability and reactivity profile. Overall, this compound's unique structure and functional groups make it a significant candidate for various chemical applications, particularly in the development of pharmaceuticals and agrochemicals.

Boronicacid, [2-(phenylmethoxy)-5-(trifluoromethyl)phenyl]- (9CI)

612833-41-7: Boronic acid, specifically 2-(phenylmethoxy)-5-(trifluoromethyl)phenyl boronic acid, 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 phenylmethoxy group and a trifluoromethyl group. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The trifluoromethyl group enhances its electronic properties, potentially increasing its lipophilicity and influencing its biological activity. Boronic acids are known for their ability to form reversible complexes with diols, which is a key feature in applications such as drug design and sensor development. Additionally, the presence of the phenylmethoxy group may contribute to the compound's stability and reactivity profile. Overall, this compound's unique structure and functional groups make it a significant candidate for various chemical applications, particularly in the development of pharmaceuticals and agrochemicals.

CAS 612833-41-7

Boronicacid, [2-(phenylmethoxy)-5-(trifluoromethyl)phenyl]- (9CI)

2-(Benzyloxy)-5-(trifluoromethyl)phenylboronic acid

Ref: IN-DA00EB48

2-Benzyloxy-5-trifluoromethylphenylboronic acid

Ref: 54-PC412079

(2-(Benzyloxy)-5-(trifluoromethyl)phenyl)boronic acid

Ref: 10-F219831