4-(2H-Tetrazol-5-yl)-phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a tetrazole moiety. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and methanol, and possessing moderate stability under standard laboratory conditions. The boronic acid group allows for reversible covalent bonding with diols and other Lewis bases, making it useful in various applications, including organic synthesis, medicinal chemistry, and as a building block in the development of pharmaceuticals. The tetrazole ring contributes to the compound's biological activity and can enhance its pharmacological properties. Additionally, the compound may exhibit interesting electronic properties due to the conjugation between the phenyl and tetrazole groups, which can influence its reactivity and interaction with biological targets. Overall, 4-(2H-tetrazol-5-yl)-phenylboronic acid is a versatile compound with significant potential in chemical research and drug development.

4-(2H-TETRAZOL-5-YL)-PHENYLBORONIC ACID

179942-55-3: 4-(2H-Tetrazol-5-yl)-phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a tetrazole moiety. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and methanol, and possessing moderate stability under standard laboratory conditions. The boronic acid group allows for reversible covalent bonding with diols and other Lewis bases, making it useful in various applications, including organic synthesis, medicinal chemistry, and as a building block in the development of pharmaceuticals. The tetrazole ring contributes to the compound's biological activity and can enhance its pharmacological properties. Additionally, the compound may exhibit interesting electronic properties due to the conjugation between the phenyl and tetrazole groups, which can influence its reactivity and interaction with biological targets. Overall, 4-(2H-tetrazol-5-yl)-phenylboronic acid is a versatile compound with significant potential in chemical research and drug development.

CAS 179942-55-3

4-(2H-TETRAZOL-5-YL)-PHENYLBORONIC ACID

4-(2H-Tetrazol-5-yl)-phenylboronic acid

Ref: IN-DA00APB5

4-(2H-Tetrazol-5-yl)-phenylboronic acid

Ref: 54-OR90433

[4-(1H-1,2,3,4-tetrazol-5-yl)phenyl]boronic acid

Ref: 10-F790678