CAS 1073339-12-4: 2-(5-Bromo-2,3-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description: 2-(5-Bromo-2,3-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structure, which includes a dioxaborolane ring and a substituted phenyl group. The presence of bromine and fluorine atoms in the phenyl ring contributes to its reactivity and potential applications in medicinal chemistry and materials science. The dioxaborolane moiety is known for its ability to participate in various chemical reactions, including Suzuki coupling, making this compound valuable in organic synthesis. Additionally, the bulky tetramethyl substituents enhance its stability and solubility in organic solvents. This compound may exhibit interesting electronic properties due to the halogen substituents, which can influence its behavior in chemical reactions and interactions with biological targets. Overall, its distinctive structural features and functional groups suggest potential utility in diverse chemical applications, particularly in the development of pharmaceuticals and advanced materials.

Formula: C₁₂H₁₄BBrF₂O₂

InChI: InChI=1S/C12H14BBrF2O2/c1-11(2)12(3,4)18-13(17-11)8-5-7(14)6-9(15)10(8)16/h5-6H,1-4H3

InChI key: InChIKey=PFZXDLSNBLEISL-UHFFFAOYSA-N

SMILES: FC=1C=C(Br)C=C(B2OC(C)(C)C(O2)(C)C)C1F

5-Bromo-2,3-difluorophenylboronic acid,pinacol ester

CAS: 1073339-12-4

• Formula: C₁₂H₁₄BBrF₂O₂
• Purity: 96%
• Color and Shape: Solid
• Molecular weight: 318.9502

5-Bromo-2,3-difluorobenzeneboronic acid, pinacol ester

CAS: 1073339-12-4

• Purity: 96%
• Molecular weight: 318.95g/mol

2-(5-Bromo-2,3-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 1073339-12-4

• Purity: 95.0%
• Molecular weight: 318.95001220703125

5-BroMo-2,3-difluorophenylboronic acid, pinacol ester

CAS: 1073339-12-4

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• Purity: Min. 95%