Boronic acid, specifically 4'-(trifluoromethoxy)[1,1'-biphenyl]-4-yl-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a biphenyl structure. This compound features a trifluoromethoxy group, which enhances its electronic properties and solubility in organic solvents. The presence of the trifluoromethoxy substituent can also influence its reactivity and interactions in various chemical reactions, particularly in Suzuki coupling reactions, where boronic acids are commonly utilized as coupling partners. The compound is likely to exhibit moderate stability under ambient conditions but may be sensitive to moisture due to the boronic acid functionality. Its unique structure makes it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the trifluoromethoxy group can impart specific biological activities, making this compound of interest in medicinal chemistry. Overall, this boronic acid derivative is a versatile building block in synthetic organic chemistry.

Boronic acid, [4'-(trifluoromethoxy)[1,1'-biphenyl]-4-yl]-

501944-50-9: Boronic acid, specifically 4'-(trifluoromethoxy)[1,1'-biphenyl]-4-yl-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a biphenyl structure. This compound features a trifluoromethoxy group, which enhances its electronic properties and solubility in organic solvents. The presence of the trifluoromethoxy substituent can also influence its reactivity and interactions in various chemical reactions, particularly in Suzuki coupling reactions, where boronic acids are commonly utilized as coupling partners. The compound is likely to exhibit moderate stability under ambient conditions but may be sensitive to moisture due to the boronic acid functionality. Its unique structure makes it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the trifluoromethoxy group can impart specific biological activities, making this compound of interest in medicinal chemistry. Overall, this boronic acid derivative is a versatile building block in synthetic organic chemistry.

(4'-(Trifluoromethoxy)-[1,1'-biphenyl]-4-yl)boronic acid

{4-[4-(Trifluoromethoxy)phenyl]phenyl}boronic acid

CAS 501944-50-9

Boronic acid, [4'-(trifluoromethoxy)[1,1'-biphenyl]-4-yl]-

(4'-(Trifluoromethoxy)-[1,1'-biphenyl]-4-yl)boronic acid

Ref: IN-DA00DKK7

{4-[4-(Trifluoromethoxy)phenyl]phenyl}boronic acid

Ref: 54-PC412550