Unlock the versatile potential of 4-(3-Pyridyl)benzeneboronic acid hydrochloride, a premium-quality boronic acid compound with a purity of 98%. This exceptional chemical, bearing the CAS number 2377369-59-8, boasts a molecular weight of 235.47g/mol, offering a unique blend of reactivity and selectivity for your advanced research and synthesis needs. Crafted with precision, this clear, pale solid form is a cornerstone for innovative applications in the fields of pharmaceuticals, agrochemicals, and beyond. Harness the power of this exceptional boronic acid derivative, and elevate your experiments to new heights of success.
Unlock the versatile potential of 4-(3-Pyridyl)benzeneboronic acid hydrochloride, a meticulously crafted chemical compound that holds the key to unlocking new frontiers in scientific research and development. This Boronic Acid and Impurities product, identified by its CAS number 2377369-59-8, is a testament to the power of precision and purity in the world of chemistry.
At the heart of this compound lies a unique molecular structure, a harmonious blend of a pyridyl group and a benzeneboronic acid moiety, all stabilized by a hydrochloride counterion. This intricate design endows 4-(3-Pyridyl)benzeneboronic acid hydrochloride with a diverse array of applications, making it a valuable asset in the hands of researchers and scientists across various disciplines.
In the realm of pharmaceutical research, this compound shines as a versatile building block for the synthesis of innovative drug candidates. Its pyridyl and boronic acid functionalities offer a wealth of opportunities for chemists to explore novel molecular scaffolds, potentially leading to the development of targeted therapies for a wide range of health conditions. The hydrochloride salt form ensures enhanced solubility and stability, crucial factors in the formulation of effective pharmaceutical products.
Researchers in the pharmaceutical industry can leverage the unique properties of 4-(3-Pyridyl)benzeneboronic acid hydrochloride to design and synthesize compounds with improved pharmacokinetic profiles, enhanced potency, and increased selectivity. This compound's adaptability allows for the exploration of diverse therapeutic areas, from oncology and neurology to metabolic disorders and beyond.
Beyond the pharmaceutical realm, 4-(3-Pyridyl)benzeneboronic acid hydrochloride finds its place in the world of agrochemicals. Its distinct chemical structure and reactivity make it a valuable building block in the development of advanced crop protection agents. Agrochemists can harness the compound's potential to create selective and potent pesticides, herbicides, or fungicides that safeguard crops while minimizing environmental impact.
The incorporation of the pyridyl and boronic acid moieties into agrochemical formulations can lead to enhanced efficacy, improved selectivity, and increased stability. This, in turn, translates to healthier crops, higher yields, and a more sustainable approach to agricultural practices – a crucial step towards a greener future.
Beyond its pharmaceutical and agrochemical applications, 4-(3-Pyridyl)benzeneboronic acid hydrochloride shines as a versatile tool in the realm of chemical synthesis. Its unique structural features and reactive functionalities make it a valuable reagent in the creation of a wide range of novel compounds and materials.
Chemists and material scientists can leverage the compound's boronic acid and pyridyl groups to explore diverse synthetic pathways, leading to the development of innovative molecules, polymers, or functional materials. These advancements can have far-reaching implications, from the design of advanced materials with enhanced properties to the exploration of new chemical transformations that push the boundaries of scientific discovery.
4-(3-Pyridyl)benzeneboronic acid hydrochloride boasts a purity of 98%, ensuring reliable and consistent results in your research endeavors. Its molecular weight of 235.47 g/mol and unique InChIKey identifier, NLNURWGCLKVUJW-UHFFFAOYSA-N, provide a clear chemical signature for easy identification and traceability.
When handling this compound, it is essential to follow standard laboratory safety protocols. Wear appropriate personal protective equipment, such as gloves, lab coat, and eye protection, and work in a well-ventilated area. Avoid direct contact with the skin, eyes, or respiratory system, and consult the relevant safety data sheets for comprehensive guidance on safe handling and storage.