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5-Acetyl-2-thiopheneboronic acid CAS:206551-43-1

5-Acetyl-2-thiopheneboronic acid is an organoboron compound characterized by a thiophene ring substituted with an acetyl group at the 5-position and a boronic acid functional group. Its molecular formula is C7H7BO2S. This compound exhibits unique chemical reactivity due to the combination of the boronic acid moiety and the functionalized thiophene ring, making it a valuable intermediate in organic synthesis. Its notable properties facilitate its application in pharmaceuticals and materials science.

 


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Application and Effect:

5-Acetyl-2-thiopheneboronic acid is widely used as a building block in organic synthesis, particularly for the development of various biologically active compounds. The boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, a powerful method for forming carbon-carbon bonds. This allows for the effective synthesis of complex aromatic compounds that are crucial in drug discovery and development. In medicinal chemistry, derivatives of 5-acetyl-2-thiopheneboronic acid have shown potential as therapeutic agents. The presence of the acetyl group enhances reactivity, contributing to the formation of diverse molecular structures that can interact with biological targets. These derivatives are being explored for their activity against conditions such as cancer and inflammatory diseases, with emphasis on optimizing their pharmacological properties for improved efficacy and safety. Furthermore, this compound plays a significant role in the synthesis of various agrochemical products. The unique structure of 5-acetyl-2-thiopheneboronic acid can lead to the development of new herbicides or pesticides, enhancing agricultural productivity and effectiveness against pests and diseases. The incorporation of the boronic acid moiety assists in improving the bioactivity and selectivity of these agrochemicals. In materials science, 5-acetyl-2-thiopheneboronic acid is utilized in the fabrication of advanced materials due to its ability to form dynamic covalent bonds. The compound’s reactivity can be harnessed to create functionalized polymers and nanomaterials suitable for various applications, including sensors, electronics, and drug delivery systems. Its versatility enables researchers to design materials with specific properties tailored for targeted applications. Moreover, the compound is also explored in the development of fluorescent probes for biological imaging, leveraging its distinctive chemical characteristics to create sensitive detection methods in biological studies. In summary, 5-acetyl-2-thiopheneboronic acid serves as a vital compound in organic synthesis, with significant applications across pharmaceuticals, agrochemicals, and materials science, highlighting its importance in advancing diverse fields of chemical research and industry.

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 C7H7BO2S
Assay 99%
Appearance white powder
CAS No.  206551-43-1
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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