[4-(Propan-2-yloxy)-2-(trifluoromethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a trifluoromethyl group, which enhances its lipophilicity and can influence its electronic properties. The propan-2-yloxy group contributes to the compound's solubility and stability. Boronic acids are typically characterized by their ability to participate in Suzuki coupling reactions, making this compound potentially valuable in the synthesis of complex organic molecules. Additionally, the presence of the trifluoromethyl group may impart unique reactivity and biological activity. Overall, this compound's structural features suggest it could be of interest in the development of pharmaceuticals or agrochemicals, where boron-containing compounds often play a significant role.

[4-(propan-2-yloxy)-2-(trifluoromethyl)phenyl]boronic acid

313545-40-3: [4-Isopropoxy-2-(trifluoromethyl)phenyl]boronic acid, boronic acid, B-[4-(1-methylethoxy)-2-(trifluoromethyl)phenyl]-, 4-Isopropoxy-2-(trifluoromethyl)phenylboronic acid

4-ISOPROPOXY-2-(TRIFLUOROMETHYL)PHENYLBORONIC ACID

(4-Isopropoxy-2-(trifluoromethyl)phenyl)boronic acid

4-Isopropoxy-2-(trifluoromethyl)benzeneboronic acid

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CAS 313545-40-3: [4-(propan-2-yloxy)-2-(trifluoromethyl)phenyl]boronic acid

4-ISOPROPOXY-2-(TRIFLUOROMETHYL)PHENYLBORONIC ACID

Ref: IN-DA00BXS7

(4-Isopropoxy-2-(trifluoromethyl)phenyl)boronic acid

Ref: 10-F219137

4-Isopropoxy-2-(trifluoromethyl)benzeneboronic acid

Ref: 54-PC3075

4-Isopropoxy-2-(Trifluoromethyl)Phenylboronic Acid

Ref: 3D-FI92159