2-(4-Fluorophenyl)-4,4,6-trimethyl-1,3,2-dioxaborinate is an organoboron compound characterized by its unique dioxaborinane structure, which features a boron atom bonded to oxygen and carbon atoms. This compound typically exhibits a high degree of stability due to the presence of the dioxaborinane ring, which can influence its reactivity and solubility in various solvents. The presence of the 4-fluorophenyl group enhances its electronic properties, potentially making it useful in applications such as pharmaceuticals, agrochemicals, and materials science. The trimethyl groups contribute to steric hindrance, which can affect the compound's reactivity and interactions with other molecules. Additionally, the fluorine atom can impart unique characteristics, such as increased lipophilicity and altered biological activity. Overall, this compound's structural features suggest potential utility in synthetic chemistry and as a building block for more complex molecules. However, specific applications and reactivity would depend on further experimental studies and context within chemical synthesis.

2-(4-FLUOROPHENYL)-4,4,6-TRIMETHYL-1,3,2-DIOXABORINATE

173341-99-6: 2-(4-Fluorophenyl)-4,4,6-trimethyl-1,3,2-dioxaborinate is an organoboron compound characterized by its unique dioxaborinane structure, which features a boron atom bonded to oxygen and carbon atoms. This compound typically exhibits a high degree of stability due to the presence of the dioxaborinane ring, which can influence its reactivity and solubility in various solvents. The presence of the 4-fluorophenyl group enhances its electronic properties, potentially making it useful in applications such as pharmaceuticals, agrochemicals, and materials science. The trimethyl groups contribute to steric hindrance, which can affect the compound's reactivity and interactions with other molecules. Additionally, the fluorine atom can impart unique characteristics, such as increased lipophilicity and altered biological activity. Overall, this compound's structural features suggest potential utility in synthetic chemistry and as a building block for more complex molecules. However, specific applications and reactivity would depend on further experimental studies and context within chemical synthesis.

<p>4-Fluorobenzeneboronic acid, hexylene glycol cyclic ester</p>

CAS 173341-99-6

2-(4-FLUOROPHENYL)-4,4,6-TRIMETHYL-1,3,2-DIOXABORINATE

4-Fluorobenzeneboronic acid, hexylene glycol cyclic ester

Ref: 54-PC10338