Boronic acids are a class of organic compounds characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. The compound "Boronic acid, [5-(trifluoromethyl)-1,3-phenylene]bis-" features a phenylene group with a trifluoromethyl substituent, which enhances its electronic properties and solubility in various solvents. This compound typically exhibits moderate stability under ambient conditions but can be sensitive to moisture, as boronic acids can hydrolyze to form boronic esters. The presence of the trifluoromethyl group can influence its reactivity, making it useful in various applications, including organic synthesis and medicinal chemistry. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is a key feature in applications such as drug delivery and sensor development. Additionally, the compound may exhibit unique properties such as fluorescence or specific catalytic activity, depending on its molecular structure and the surrounding environment. Overall, this boronic acid derivative is of interest in both academic research and industrial applications.

Boronic acid, [5-(trifluoromethyl)-1,3-phenylene]bis-

913835-35-5: Boronic acids are a class of organic compounds characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. The compound "Boronic acid, [5-(trifluoromethyl)-1,3-phenylene]bis-" features a phenylene group with a trifluoromethyl substituent, which enhances its electronic properties and solubility in various solvents. This compound typically exhibits moderate stability under ambient conditions but can be sensitive to moisture, as boronic acids can hydrolyze to form boronic esters. The presence of the trifluoromethyl group can influence its reactivity, making it useful in various applications, including organic synthesis and medicinal chemistry. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is a key feature in applications such as drug delivery and sensor development. Additionally, the compound may exhibit unique properties such as fluorescence or specific catalytic activity, depending on its molecular structure and the surrounding environment. Overall, this boronic acid derivative is of interest in both academic research and industrial applications.

CAS 913835-35-5

Boronic acid, [5-(trifluoromethyl)-1,3-phenylene]bis-

5-Trifluoromethyl-1,3-phenylenediboronic acid

Ref: IN-DA006NKP

5-(Trifluoromethyl)benzene-1,3-diboronic acid

Ref: 54-PC5119