CAS · 363166-79-4
Product Overview
2,6-Diisopropylphenylboronic acid is a high-purity borane supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.
Product Specifications
| Appearance | Off-white solid |
|---|---|
| Purity (HPLC) | 98.0% min. |
| Water (KF) | 0.5% max. |
| HNMR | Conform to the structure |
Applications
2,6-Diisopropylphenylboronic acid is primarily used in organic synthesis and pharmaceutical research as a key intermediate for cross-coupling reactions, particularly Suzuki-Miyaura couplings. It serves as a building block for the preparation of biaryl compounds, heterocycles, and functionalized aromatic molecules used in drug discovery, agrochemicals, and materials science. The compound is also employed in research to study boronic acid reactivity, develop novel catalytic systems, and synthesize ligands or functional molecules for advanced materials, including organic electronic devices and sensors.
Benefits
2,6-Diisopropylphenylboronic acid offers several advantages in chemical and pharmaceutical applications. The sterically hindered diisopropyl groups provide enhanced selectivity in cross-coupling reactions, reducing side reactions and improving yields of target products. Its boronic acid functionality allows efficient formation of carbon–carbon bonds under mild conditions, making it versatile for multi-step synthesis. The compound's stability and well-defined structure ensure reproducible reactivity and reliability in both research and industrial applications. Additionally, it supports rapid exploration of chemical libraries and the creation of complex, functionalized molecules for pharmaceuticals and materials research.
Conclusion
2,6-Diisopropylphenylboronic acid is a versatile intermediate widely used in organic synthesis, pharmaceuticals, and materials science. Its sterically protected boronic acid group enables selective coupling reactions and efficient construction of complex molecules. Overall, 2,6-Diisopropylphenylboronic acid supports high-yield synthesis, structural diversification, and development of bioactive and functional compounds.
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