1H-imidazole-2-boronic acid hydrochloride

Unlock the versatile potential of 1H-imidazole-2-boronic acid hydrochloride, a highly specialized chemical compound that holds immense value for researchers and scientists across various fields. This unique heterocyclic compound, identified by its CAS number 1919022-57-3, boasts a remarkable combination of properties that make it an indispensable tool in the pursuit of scientific discovery.

At the heart of this compound lies the imidazole ring, a nitrogen-containing heterocycle that serves as a foundational structure in numerous biologically active molecules. The addition of the boronic acid moiety and the hydrochloride salt form further enhances the compound's versatility, opening up a wide range of applications in the realms of pharmaceutical research, organic synthesis, and material science.

With a purity of 95% or higher, this 1H-imidazole-2-boronic acid hydrochloride offers researchers the confidence to rely on its consistent performance and reliable results. Its molecular formula of C3H5BN2O2·ClH and a molecular weight of 148.36g/mol provide a unique chemical identity that can be easily tracked and referenced throughout your research endeavors.

Pharmaceutical Research: Unlocking New Therapeutic Possibilities

In the dynamic field of pharmaceutical research, 1H-imidazole-2-boronic acid hydrochloride shines as a versatile building block for the synthesis of innovative drug candidates. The imidazole core, combined with the boronic acid functionality, allows for the creation of diverse molecular scaffolds that can be tailored to target a wide range of health conditions, from neurological disorders to metabolic diseases.

Researchers leveraging this compound can explore the development of novel therapeutic agents, harnessing the unique properties of the imidazole-boronic acid system to enhance pharmacological profiles, improve bioavailability, and unlock new avenues for targeted drug delivery. The compound's potential to participate in a variety of chemical reactions, such as cross-coupling, cycloaddition, and borylation, further expands the possibilities for pharmaceutical researchers to push the boundaries of drug discovery.

Organic Synthesis: A Versatile Reagent for Chemical Innovation

Beyond the pharmaceutical realm, 1H-imidazole-2-boronic acid hydrochloride finds its place as a valuable reagent in the realm of organic synthesis. Its distinct chemical structure and reactivity make it a powerful tool in the hands of chemists seeking to create novel compounds with tailored properties.

The boronic acid functionality, in particular, allows for the incorporation of this compound into a wide range of synthetic transformations, including Suzuki-Miyaura cross-coupling, borylation reactions, and the formation of heterocyclic scaffolds. These versatile applications enable chemists to explore the synthesis of complex molecules, unlock new pathways for the construction of diverse chemical entities, and ultimately contribute to the advancement of materials science, agrochemicals, and other interdisciplinary fields.

Material Science: Enhancing Performance with Imidazole-Boronic Acid Derivatives

In the realm of material science, 1H-imidazole-2-boronic acid hydrochloride finds its niche as a building block for the development of innovative materials with enhanced performance characteristics. Researchers can leverage the unique properties of this compound to engineer polymers, coatings, or functional materials with improved thermal stability, mechanical strength, or optical properties.

The imidazole-boronic acid moiety can be strategically incorporated into the design of new materials, allowing for the tailoring of their chemical and physical attributes. This versatility opens up avenues for the creation of advanced materials with applications in areas such as energy storage, catalysis, sensors, and beyond, ultimately contributing to the advancement of technology and the betterment of our world.

Handling and Storage: Ensuring Optimal Stability and Safety

As with any specialized chemical compound, proper handling and storage of 1H-imidazole-2-boronic acid hydrochloride are crucial to maintain its integrity and ensure safe usage. This compound is classified as an