
Catalog Number	AR007FH3
Chemical Name	(5-Cyano-2-(trifluoromethoxy)phenyl)boronic acid
CAS Number	1072946-64-5
Molecular Formula	C8H5BF3NO3
Molecular Weight	230.9364
MDL Number	MFCD11053857
SMILES	N#Cc1ccc(c(c1)B(O)O)OC(F)(F)F

(5-Cyano-2-(trifluoromethoxy)phenyl)boronic acid is a versatile chemical compound widely used in organic synthesis, specifically in the field of medicinal chemistry and material science. Its unique structure containing both a cyano group and a trifluoromethoxy group makes it a valuable building block for the construction of complex molecules with diverse functionalities.In chemical synthesis, this Boronic acid derivative serves as a key reagent for Suzuki-Miyaura cross-coupling reactions, a popular method for forming carbon-carbon bonds. By participating in these coupling reactions, (5-Cyano-2-(trifluoromethoxy)phenyl)boronic acid enables the efficient and selective synthesis of biaryl compounds, which are commonly found in pharmaceuticals, agrochemicals, and materials science.Additionally, this compound can also act as a versatile precursor for the introduction of the cyano and trifluoromethoxy moieties into target molecules. The cyano group can serve as a directing group in various C-H functionalization reactions, allowing for regioselective modifications, while the trifluoromethoxy group can impart desirable physicochemical properties to the final products.Overall, the application of (5-Cyano-2-(trifluoromethoxy)phenyl)boronic acid in chemical synthesis offers chemists a powerful tool for the efficient construction of complex molecules with tailored properties, making it a valuable asset in the pursuit of new drug candidates, advanced materials, and other innovative compounds.