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2-Methoxypyrimidine-5-boronic acid CAS:628692-15-9

2-Methoxypyrimidine-5-boronic acid is an organoboron compound featuring a pyrimidine ring with a methoxy group at the 2-position and a boronic acid functional group at the 5-position. Its molecular formula is C6H8BNO3. This compound is known for its unique reactivity, making it an important building block in organic synthesis. The presence of the methoxy group enhances electronic properties, facilitating participation in various coupling reactions, which are crucial in the development of pharmaceuticals and advanced materials.

 


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Application and Effect:

2-Methoxypyrimidine-5-boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This method allows for the efficient formation of carbon-carbon bonds between aryl halides and boronic acids, enabling the construction of complex organic molecules. The reactivity of 2-methoxypyrimidine-5-boronic acid makes it a valuable intermediate in the synthesis of diverse bioactive compounds, which are essential in drug development. In medicinal chemistry, derivatives of 2-methoxypyrimidine-5-boronic acid have garnered attention for their potential therapeutic activities. The methoxy group can enhance solubility and influence the pharmacokinetic properties of the resulting compounds, making them suitable candidates for various treatment applications, including cancer and infectious diseases. Research is ongoing to optimize these derivatives to improve their efficacy, selectivity, and safety, aiming to develop innovative drug candidates. Additionally, this compound has significant applications in agrochemistry. It can be employed as a precursor for the synthesis of novel pesticides and herbicides. The unique combination of the methoxy and boronic acid functionalities contributes to enhanced activity and specificity of agrochemical agents, facilitating effective pest and weed control in sustainable agricultural practices. 2-methoxypyrimidine-5-boronic acid also plays a pivotal role in materials science. Its reactivity can be harnessed for the synthesis of functional materials and advanced polymers through dynamic covalent chemistry. These materials may find applications in areas such as organic electronics, sensors, and drug delivery systems, where customizable properties are essential. Moreover, there is ongoing research into the potential use of 2-methoxypyrimidine-5-boronic acid in biological imaging applications. Its chemical characteristics can be utilized to develop fluorescent probes that enable visualization of biological processes and cellular functions, thereby advancing techniques in biochemical research and diagnostics. In summary, 2-methoxypyrimidine-5-boronic acid serves as a crucial building block in organic synthesis, with versatile applications in pharmaceuticals, agrochemicals, and materials science, highlighting its significance in driving advancements across multiple research domains.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C6H8BNO3
Assay 99%
Appearance white powder
CAS No.  628692-15-9
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

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