1-(2-Chloropyridine-4-carbonyl)piperazine

Introducing 1-(2-Chloropyridine-4-carbonyl)piperazine, a versatile and highly specialized chemical compound that holds immense potential for researchers and scientists across various fields. With its unique molecular structure and exceptional purity, this compound has become a valuable asset in the realms of pharmaceutical development, agrochemical innovation, and advanced material synthesis.

At the heart of this compound lies a captivating combination of a 2-chloropyridine moiety and a piperazine ring, creating a distinct chemical profile that sets it apart. The CAS number 1354087-52-7 and the product reference 3D-EEC08752 provide a clear identification for this remarkable substance, ensuring seamless integration into your research projects.

With a purity of at least 95%, this 1-(2-Chloropyridine-4-carbonyl)piperazine offers a reliable and consistent foundation for your experiments and syntheses. Its molecular formula of C10H12ClN3O and a molecular weight of 225.67 g/mol further underscore its precise and well-defined structure, allowing for meticulous control and predictable outcomes in your research endeavors.

Pharmaceutical Research: Unlocking New Possibilities

In the dynamic field of pharmaceutical research, 1-(2-Chloropyridine-4-carbonyl)piperazine shines as a versatile building block. Its unique chemical properties and structural features make it an invaluable tool in the synthesis of innovative drug candidates, targeting a wide range of therapeutic areas. From neurological disorders to metabolic conditions, this compound's potential to contribute to the development of life-changing pharmaceuticals is truly remarkable.

The presence of the chloropyridine and piperazine moieties within the molecule endows it with a distinct reactivity profile, enabling chemists to explore novel synthetic pathways and create novel molecular structures with enhanced pharmacological properties. By leveraging the versatility of this compound, researchers can unlock new avenues for therapeutic breakthroughs, ultimately improving patient outcomes and transforming lives.

Agrochemical Innovation: Cultivating a Greener Future

Beyond the pharmaceutical realm, 1-(2-Chloropyridine-4-carbonyl)piperazine also finds its place in the dynamic world of agrochemicals. Its chemical structure and properties make it a valuable asset in the development of advanced crop protection agents, contributing to the creation of more potent and selective pesticides and herbicides.

By incorporating this compound into the synthesis of agrochemical formulations, researchers can develop innovative solutions that not only safeguard crops but also minimize environmental impact. The unique combination of the chloropyridine and piperazine moieties within the molecule can lead to the creation of highly targeted and effective agrochemical products, promoting healthier crops, higher yields, and a more sustainable agricultural landscape.

Material Science Advancements: Unlocking New Frontiers

Beyond the realms of pharmaceuticals and agrochemicals, 1-(2-Chloropyridine-4-carbonyl)piperazine also finds application in the exciting field of material science. Its distinct chemical structure and properties can be leveraged to engineer novel materials with enhanced performance characteristics, such as improved mechanical strength, thermal stability, or optical properties.

By integrating this compound into the synthesis of polymers, coatings, or other advanced materials, researchers can unlock new possibilities in areas like energy storage, electronics, and beyond. The versatility of 1-(2-Chloropyridine-4-carbonyl)piperazine allows for the creation of tailored materials with unique functionalities, driving innovation and pushing the boundaries of what's possible in material science.

Handling and Storage: Ensuring Optimal Performance

To maintain the exceptional quality and purity of 1-(2-Chloropyridine-4-carbonyl)piperazine, it is essential to adhere to proper handling and storage protocols. This compound should be handled with care, following standard laboratory safety procedures, including the use of personal protective equipment (PPE) such as gloves, lab coats, and eye protection.