Ethyl 3-cyano-6-phenylpyridine-2-carboxylate

Ethyl 3-cyano-6-phenylpyridine-2-carboxylate, with the CAS number 1221792-25-1, is a versatile and highly pure chemical compound that holds immense potential for researchers and scientists across various fields. This Pyridine derivative, characterized by its distinct molecular structure, offers a wealth of applications that can unlock new frontiers in pharmaceutical development, agrochemical innovation, and beyond.

At the heart of this compound lies a captivating combination of a cyano group, a phenyl ring, and a carboxylate ester, all seamlessly integrated within a pyridine backbone. This unique chemical architecture endows Ethyl 3-cyano-6-phenylpyridine-2-carboxylate with a remarkable set of properties, making it a valuable asset in the pursuit of scientific breakthroughs.

Pharmaceutical Research: Unlocking New Therapeutic Possibilities

In the realm of pharmaceutical research, Ethyl 3-cyano-6-phenylpyridine-2-carboxylate shines as a versatile building block for the synthesis of innovative drug candidates. Its pyridine core, coupled with the strategic placement of the cyano and phenyl moieties, allows for the development of compounds with enhanced pharmacological profiles. Researchers can leverage this compound to explore new therapeutic avenues, targeting a wide range of health conditions, from neurological disorders to metabolic diseases.

The intricate interplay of functional groups within Ethyl 3-cyano-6-phenylpyridine-2-carboxylate enables the creation of diverse molecular scaffolds, each with the potential to unlock novel mechanisms of action. This flexibility empowers scientists to design and synthesize novel drug candidates with improved potency, selectivity, and safety, ultimately leading to more effective and personalized treatments for patients.

Agrochemical Innovation: Cultivating Sustainable Solutions

Beyond the pharmaceutical realm, Ethyl 3-cyano-6-phenylpyridine-2-carboxylate also finds its place in the dynamic world of agrochemicals. Its unique chemical structure can be leveraged to develop advanced crop protection agents, such as pesticides and herbicides, that are both highly effective and environmentally responsible.

The strategic incorporation of the cyano and phenyl groups within the pyridine framework allows for the creation of targeted agrochemical compounds. These compounds can exhibit enhanced selectivity, effectively combating pests and weeds while minimizing the impact on beneficial organisms and the surrounding ecosystem. This approach aligns with the growing demand for sustainable agricultural practices that prioritize both productivity and environmental stewardship.

Chemical Synthesis: Unlocking Molecular Diversity

In the broader realm of chemical synthesis, Ethyl 3-cyano-6-phenylpyridine-2-carboxylate serves as a versatile and valuable reagent. Its distinct molecular architecture, with the interplay of the cyano, phenyl, and carboxylate ester groups, allows for a wide range of chemical transformations and the creation of novel compounds with tailored properties.

Researchers and chemists can leverage the reactivity and selectivity of Ethyl 3-cyano-6-phenylpyridine-2-carboxylate to explore new synthetic pathways, leading to the development of materials, intermediates, and other specialized chemicals. This compound's potential extends beyond the realms of pharmaceuticals and agrochemicals, opening up possibilities in fields such as materials science, organic electronics, and beyond.

Technical Specifications and Handling

Ethyl 3-cyano-6-phenylpyridine-2-carboxylate is a high-purity compound, with a purity of 95% or higher, ensuring reliable and consistent results in research and development applications. Its molecular weight of 252.27g/mol and melting point range of 99-101°C further contribute to its desirable characteristics.

Given the potential hazards associated with this compound, it is essential to handle it with appropriate safety precautions.