Ethyl 6-bromo-4-hydroxy-7-(trifluoromethyl)quinoline-3-carboxylate

Ethyl 6-bromo-4-hydroxy-7-(trifluoromethyl)quinoline-3-carboxylate, with the CAS number 1065102-42-2, is a highly specialized and versatile Fluorinated Compound that holds immense potential for researchers and scientists across various fields. This meticulously crafted chemical compound, with its unique structural features, offers a wealth of opportunities for innovative applications in the realms of pharmaceutical development, agrochemical advancements, and beyond.

At the heart of this compound lies a quinoline backbone, adorned with a bromine substituent, a trifluoromethyl group, and a carboxylate ester. This intricate molecular architecture endows Ethyl 6-bromo-4-hydroxy-7-(trifluoromethyl)quinoline-3-carboxylate with exceptional chemical properties, making it a valuable asset in the pursuit of groundbreaking discoveries and advancements.

Pharmaceutical Research and Development

In the dynamic field of pharmaceutical research, this compound shines as a crucial building block for the synthesis of innovative drug candidates. Its unique structural features, including the trifluoromethyl moiety and the quinoline core, allow for the development of targeted therapies addressing a wide range of health conditions. Researchers can leverage the versatility of Ethyl 6-bromo-4-hydroxy-7-(trifluoromethyl)quinoline-3-carboxylate to explore new avenues in drug discovery, unlocking the potential for more effective and personalized treatments.

The compound's ability to participate in a variety of chemical reactions, coupled with its high purity and stability, make it an invaluable tool in the hands of pharmaceutical scientists. By incorporating this versatile building block into their synthetic strategies, they can create novel molecular entities with enhanced pharmacological profiles, improved bioavailability, and increased therapeutic efficacy.

Agrochemical Innovations

Beyond the pharmaceutical realm, Ethyl 6-bromo-4-hydroxy-7-(trifluoromethyl)quinoline-3-carboxylate also finds its niche in the dynamic field of agrochemical development. Its unique structural features, particularly the trifluoromethyl group, contribute to the creation of advanced crop protection agents with enhanced potency and selectivity.

Researchers in the agrochemical industry can leverage the compound's properties to develop innovative pesticides, herbicides, and fungicides that effectively target pests and diseases while minimizing environmental impact. The incorporation of Ethyl 6-bromo-4-hydroxy-7-(trifluoromethyl)quinoline-3-carboxylate into their formulations can lead to the development of more sustainable and efficient agrochemical solutions, ultimately benefiting agricultural productivity and food security.

Chemical Synthesis and Material Science

Beyond its applications in the pharmaceutical and agrochemical realms, Ethyl 6-bromo-4-hydroxy-7-(trifluoromethyl)quinoline-3-carboxylate also finds utility in the broader field of chemical synthesis and material science. Its versatile chemical properties and structural complexity make it a valuable reagent and building block for the creation of novel compounds and materials with tailored characteristics.

Researchers in material science can explore the integration of this compound into polymers, coatings, or other advanced materials, leveraging its unique properties to enhance performance characteristics such as thermal stability, mechanical strength, or optical properties. The incorporation of Ethyl 6-bromo-4-hydroxy-7-(trifluoromethyl)quinoline-3-carboxylate can lead to the development of innovative materials with applications across diverse industries, from electronics to energy storage.

Technical Specifications and Safety Considerations

Ethyl 6-bromo-4-hydroxy-7-(trifluoromethyl)quinoline-3-carboxylate is a solid compound with a molecular weight of 364.11g/mol and a distinct MDL number,