2-[4-(Difluoromethoxy)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 atom in a cyclic arrangement. This compound contains a difluoromethoxy substituent on a phenyl ring, contributing to its chemical reactivity and potential applications in medicinal chemistry and materials science. The presence of the difluoromethoxy group enhances its lipophilicity and may influence its biological activity. The tetramethyl groups provide steric hindrance, which can affect the compound's stability and reactivity. Typically, compounds like this are of interest in the development of pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. Additionally, the boron atom can participate in various chemical reactions, including cross-coupling reactions, making it valuable in synthetic organic chemistry. Overall, the unique structural features of this compound suggest a range of potential applications, particularly in fields that leverage boron chemistry.

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

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CAS 887757-48-4: 2-[4-(difluoromethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

4-Difluoromethoxyphenylboronic acid pinacol ester

Ref: 3D-FD103331

4-Difluoromethoxyphenylboronic acid pinacol ester

Ref: IN-DA008B59

4-(Difluoromethoxy)phenylboronic acid pinacol ester

Ref: FT-D10083

2-(4-(Difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Ref: 10-F212520

4-Difluoromethoxyphenylboronic acid, pinacol ester

Ref: 54-PC412369