3-Fluorophenylboronic Acid: A Versatile Building Block for Advanced Synthesis

Unlock new possibilities in pharmaceutical and material science with this key Suzuki-Miyaura coupling reagent.

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Key Advantages

Enhanced Selectivity

The meta-fluorine substituent on 3-Fluorophenylboronic Acid significantly enhances electronic modulation, leading to superior selectivity in aryl-aryl bond formation via Suzuki-Miyaura coupling.

Broad Synthetic Utility

Its versatile application spans pharmaceutical synthesis, material science, and the development of PET tracers, making it a valuable asset across multiple research and industrial domains.

Reliable Performance

With a high purity of ≥98% (HPLC) and a well-defined melting point, this boronic acid ensures dependable and reproducible results in complex organic transformations.

Key Applications

Pharmaceutical Synthesis

Crucial for constructing complex molecular architectures found in many pharmaceutical compounds through Suzuki-Miyaura coupling.

Material Science

Enables the synthesis of advanced materials with tailored electronic and structural properties.

PET Tracer Development

Its fluorinated nature makes it suitable for incorporation into molecules used in Positron Emission Tomography imaging.

Covalent Organic Frameworks

A key building block for creating porous COFs with applications in gas storage, catalysis, and separation.