7-Hydroxy-N-(3-(trifluoromethyl)phenyl)quinoline-4-carboxamide

Unlock the versatile potential of 7-Hydroxy-N-(3-(trifluoromethyl)phenyl)quinoline-4-carboxamide, a meticulously crafted chemical compound that holds the key to unlocking new frontiers in scientific research and development. With its unique molecular structure and exceptional purity, this Fluorinated Compound stands as a valuable asset for researchers and chemists across diverse fields, from pharmaceuticals to material science.

Boasting a molecular weight of 332.28g/mol and a CAS number that is yet to be assigned, this compound is a testament to the relentless pursuit of innovation. Its chemical identity, represented by the MDL number MFCD27501024, serves as a distinct identifier, allowing researchers to seamlessly integrate it into their cutting-edge projects.

The compound's core features a quinoline-4-carboxamide backbone, adorned with a 7-hydroxy group and a 3-(trifluoromethyl)phenyl substituent. This unique combination of functional groups endows 7-Hydroxy-N-(3-(trifluoromethyl)phenyl)quinoline-4-carboxamide with a remarkable versatility, unlocking a world of possibilities in the realms of chemical synthesis, pharmaceutical research, and material science.

Pharmaceutical Research: Unlocking New Therapeutic Frontiers

In the dynamic landscape of pharmaceutical research, 7-Hydroxy-N-(3-(trifluoromethyl)phenyl)quinoline-4-carboxamide shines as a pivotal building block. Its distinct chemical structure allows researchers to leverage its potential in the development of innovative drug candidates, targeting a wide spectrum of health conditions. The presence of the trifluoromethyl group and the quinoline-4-carboxamide core imbues the compound with unique pharmacological properties, paving the way for the creation of novel therapeutics with enhanced efficacy and specificity.

By seamlessly integrating this versatile compound into their synthetic strategies, pharmaceutical researchers can unlock new avenues for addressing unmet medical needs, from neurological disorders to metabolic diseases. The compound's adaptability and purity ensure reliable results, empowering scientists to push the boundaries of pharmaceutical innovation.

Agrochemical Innovation: Cultivating a Sustainable Future

Beyond the realm of pharmaceuticals, 7-Hydroxy-N-(3-(trifluoromethyl)phenyl)quinoline-4-carboxamide also finds its niche in the dynamic field of agrochemicals. Its unique chemical properties make it a valuable building block in the synthesis of advanced crop protection agents, contributing to the development of more potent and selective pesticides.

By leveraging the compound's distinct molecular structure, agrochemical researchers can formulate innovative solutions that safeguard crops while minimizing environmental impact. The integration of 7-Hydroxy-N-(3-(trifluoromethyl)phenyl)quinoline-4-carboxamide into their research and development efforts empowers scientists to cultivate a sustainable future, where increased crop yields and healthier ecosystems go hand in hand.

Material Science Innovations: Unlocking the Potential of Novel Materials

Beyond the realms of pharmaceuticals and agrochemicals, 7-Hydroxy-N-(3-(trifluoromethyl)phenyl)quinoline-4-carboxamide also finds its place in the exciting world of material science. Its versatile chemical structure and exceptional purity make it a valuable tool for researchers seeking to engineer novel materials with tailored properties.

By incorporating this compound into their synthetic strategies, material scientists can unlock the potential of new materials with enhanced mechanical strength, thermal stability, or optical characteristics. The unique combination of functional groups within 7-Hydroxy-N-(3-(trifluoromethyl)phenyl)quinoline-4-carboxamide allows for the creation of innovative polymers, coatings, or advanced composites, opening up a world of possibilities for diverse applications.

Technical Specifications and Safety Considerations