2-[4-(4-Fluorophenoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a boron atom bonded to two oxygen atoms and a carbon framework. This compound contains a fluorophenoxy group, which enhances its potential for applications in medicinal chemistry and materials science due to the electron-withdrawing properties of the fluorine atom. The presence of tetramethyl groups contributes to its steric bulk, influencing its reactivity and solubility. Typically, compounds like this exhibit stability under ambient conditions but may undergo hydrolysis in the presence of moisture, releasing boric acid derivatives. Its structure suggests potential utility in cross-coupling reactions, particularly in the synthesis of complex organic molecules. Additionally, the presence of the dioxaborolane moiety may facilitate the formation of boronate esters, which are valuable intermediates in organic synthesis. Overall, this compound's unique structural features make it a subject of interest in various chemical research fields.

2-[4-(4-fluorophenoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1355052-34-4: 2-[4-(4-Fluorophenoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a boron atom bonded to two oxygen atoms and a carbon framework. This compound contains a fluorophenoxy group, which enhances its potential for applications in medicinal chemistry and materials science due to the electron-withdrawing properties of the fluorine atom. The presence of tetramethyl groups contributes to its steric bulk, influencing its reactivity and solubility. Typically, compounds like this exhibit stability under ambient conditions but may undergo hydrolysis in the presence of moisture, releasing boric acid derivatives. Its structure suggests potential utility in cross-coupling reactions, particularly in the synthesis of complex organic molecules. Additionally, the presence of the dioxaborolane moiety may facilitate the formation of boronate esters, which are valuable intermediates in organic synthesis. Overall, this compound's unique structural features make it a subject of interest in various chemical research fields.

CAS 1355052-34-4

2-[4-(4-fluorophenoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

2-[4-(4-fluorophenoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Ref: IN-DA01CCS3

2-[4-(4-fluorophenoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Ref: 54-PC102875

2-[4-(4-fluorophenoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Ref: 10-F791923