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2-Formylfuran-5-boronic acid CAS:27329-70-0

2-Formylfuran-5-boronic acid is a chemical compound characterized by its boronic acid group attached to a furan ring with a formyl substituent. It is utilized in organic synthesis as a versatile building block due to its ability to form stable boronate esters and its reactivity in cross-coupling reactions. The compound’s structure facilitates its integration into various molecular frameworks, making it valuable in pharmaceutical and agrochemical research.

 


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Application and Effect:

2-Formylfuran-5-boronic acid plays a crucial role in organic synthesis, particularly in the development of novel pharmaceuticals, agrochemicals, and advanced materials. Its utility stems from its structural features and chemical properties: Building Block in Organic Synthesis: The boronic acid moiety in 2-formylfuran-5-boronic acid enables it to participate in Suzuki-Miyaura cross-coupling reactions, a key method for creating carbon-carbon bonds. This versatility allows for the synthesis of complex organic molecules. Pharmaceutical Applications: The compound is employed in medicinal chemistry to synthesize bioactive molecules and potential drug candidates. Its furan scaffold and boronic acid functionality are particularly advantageous in designing molecules with specific biological activities. Agrochemical Research: In the field of agrochemicals, 2-formylfuran-5-boronic acid is utilized to develop new pesticides and herbicides. Its structural flexibility allows chemists to tailor compounds that exhibit selective activity against pests and weeds while minimizing environmental impact. Materials Science: Researchers utilize this compound in the synthesis of advanced materials such as functional polymers and organic electronic materials. Its incorporation into these materials enhances their properties, including conductivity, stability, and responsiveness. Catalysis: Beyond its role as a building block, 2-formylfuran-5-boronic acid serves as a catalyst or ligand in various chemical transformations. Its boron center can coordinate with metals, influencing reaction pathways and improving efficiency in catalytic processes. Research Tool: Chemists also employ 2-formylfuran-5-boronic acid as a research tool to study chemical reactions and explore new synthetic methodologies. Its predictable reactivity and stability under certain conditions make it valuable in experimental settings. In conclusion, 2-formylfuran-5-boronic acid is a multifaceted compound with wide-ranging applications in organic synthesis, pharmaceuticals, agrochemicals, materials science, and catalysis. Its structural adaptability and functional diversity continue to inspire innovations across various scientific disciplines, contributing to advancements in both academic research and industrial applications.

Product Sample:

Amino acid powder1
Amino acid powder2

Product Packing:

Amino acid powder3
Amino acid powder4
Amino acid powder5
Amino acid powder6

Additional Information:

Composition C5H5BO4
Assay 99%
Appearance white powder
CAS No.  27329-70-0
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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