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3-Tolylboronic acid CAS:17933-03-8

3-Tolylboronic acid is a boronic acid compound characterized by a boronic acid group attached to a phenyl ring substituted with a methyl group at the 3-position. This compound holds significance in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile boronic acid reagent. Additionally, its structural features make it valuable in medicinal chemistry, materials science, and the synthesis of specialized organic compounds.


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Application and Effect:

3-Tolylboronic acid exhibits unique structural attributes and versatile applications across various fields of chemistry. 1. Synthetic Chemistry: Suzuki-Miyaura Cross-Coupling: Widely employed in Suzuki-Miyaura cross-coupling reactions, 3-tolylboronic acid facilitates the synthesis of biaryl compounds. Its versatility as a boronic acid reagent enables the construction of complex organic molecules, essential in pharmaceuticals, agrochemicals, and materials science. 2. Medicinal Chemistry: Drug Development: The presence of a methyl group at the 3-position of the phenyl ring influences the compound's interactions with biological targets, making it valuable in drug discovery. Derivatives of 3-tolylboronic acid are explored for their potential as therapeutic agents targeting various diseases, including cancer, inflammation, and metabolic disorders. Enzyme Inhibition: Functionalized derivatives of this compound are investigated for their ability to inhibit specific enzymes implicated in disease pathways, offering potential therapeutic interventions. 3. Materials Science: Polymer Synthesis: Incorporated into polymers, 3-tolylboronic acid derivatives modify properties such as solubility, conductivity, and mechanical strength. These tailored polymers find applications in coatings, adhesives, and biomedical materials. Organic Electronics: Utilized in the fabrication of organic electronic devices, such as OLEDs and OFETs, owing to its electron-rich nature and compatibility with semiconductor materials. 4. Organic Synthesis: Functional Group Tolerance: The methyl group on the phenyl ring imparts specific reactivity profiles, enabling selective transformations and compatibility with various functional groups in organic synthesis. This versatility allows for the synthesis of diverse organic molecules with precise control over structure and functionality. In summary, 3-tolylboronic acid is a versatile compound with broad utility in synthetic chemistry, medicinal chemistry, materials science, and organic synthesis. Its distinct structural features and reactivity offer opportunities for innovation and advancement across multiple scientific disciplines, contributing to the development of novel molecules, materials, and pharmaceutical agents.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C7H9BO2
Assay 99%
Appearance white powder
CAS No.  17933-03-8
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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