High-Purity 2,4-Difluorophenylboronic Acid: A Versatile Building Block for Suzuki Coupling and Advanced Synthesis

Unlock new frontiers in chemical synthesis with 2,4-difluorophenylboronic acid, a premium reagent essential for Suzuki-Miyaura cross-coupling and the creation of innovative pharmaceuticals and materials.

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Advantages Offered

Enhanced Reactivity & Selectivity

The unique difluoro substitution on the phenyl ring significantly enhances the reactivity and selectivity of this boronic acid derivative in cross-coupling reactions, contributing to more efficient organic synthesis building blocks.

Versatility in Applications

Its broad applicability spans from intricate pharmaceutical intermediates synthesis to the development of cutting-edge materials, showcasing its role as a versatile chemical tool.

Facilitates Complex Molecule Synthesis

As a critical component for the Suzuki-Miyaura reaction mechanism, it enables the formation of carbon-carbon bonds, essential for constructing complex organic structures with high efficiency.

Key Applications

Organic Synthesis

A fundamental reagent in organic synthesis building blocks, enabling precise C-C bond formation through Suzuki coupling reactions.

Medicinal Chemistry

Crucial for creating novel pharmaceutical intermediates and drug candidates, particularly in areas like oncology and diabetes research.

Material Science

Utilized in the development of advanced polymers and novel sensors, contributing to enhanced material properties and functionalities.

Agrochemicals Development

Serves as a key intermediate in the synthesis of various agrochemicals, contributing to crop protection and agricultural innovation.