2-{[2-(Trifluoromethyl)quinolin-4-yl]amino}ethanethiol

Unlock the versatile potential of 2-{[2-(Trifluoromethyl)quinolin-4-yl]amino}ethanethiol, a highly specialized Fluorinated Compound that holds the key to unlocking new frontiers in scientific research and development. This captivating chemical, identified by its CAS number 1065076-10-9, boasts a unique molecular structure that sets it apart as a valuable asset in the realms of pharmaceuticals, agrochemicals, and beyond.

Crafted with meticulous precision, this compound presents itself as a clear, pale yellow liquid, with a molecular weight of 272.29g/mol. Its distinct trifluoromethyl-substituted quinoline core, coupled with the presence of an ethanethiol moiety, endows it with a remarkable chemical profile that can be leveraged to drive innovative breakthroughs.

Unlocking the Potential in Pharmaceutical Research

In the dynamic world of pharmaceutical research, 2-{[2-(Trifluoromethyl)quinolin-4-yl]amino}ethanethiol shines as a versatile building block. Its intricate structure allows for the synthesis of novel drug candidates, targeting a wide spectrum of health conditions. Researchers can harness the compound's reactivity and selectivity to develop innovative therapies with enhanced pharmacological properties, ultimately improving patient outcomes and transforming lives.

The trifluoromethyl group, a hallmark of this compound, contributes to increased metabolic stability and improved bioavailability, making it a valuable asset in the pursuit of more effective and safer pharmaceutical solutions. By leveraging the unique properties of 2-{[2-(Trifluoromethyl)quinolin-4-yl]amino}ethanethiol, scientists can unlock new possibilities in the treatment of complex diseases, driving the pharmaceutical industry forward with groundbreaking discoveries.

Revolutionizing Agrochemical Innovation

Beyond the realm of pharmaceuticals, this captivating Fluorinated Compound also finds its place in the dynamic world of agrochemicals. Its distinct molecular structure and chemical reactivity make it a crucial building block in the synthesis of advanced crop protection agents, empowering researchers to develop more potent and selective pesticides.

The incorporation of the trifluoromethyl moiety and the ethanethiol functionality into agrochemical formulations can lead to enhanced efficacy, improved target specificity, and reduced environmental impact. By harnessing the power of 2-{[2-(Trifluoromethyl)quinolin-4-yl]amino}ethanethiol, scientists can unlock new frontiers in sustainable agriculture, contributing to increased crop yields, healthier ecosystems, and a more secure global food supply.

Versatility in Chemical Synthesis

The versatility of 2-{[2-(Trifluoromethyl)quinolin-4-yl]amino}ethanethiol extends beyond its pharmaceutical and agrochemical applications. This compound serves as a valuable reagent and building block in the realm of chemical synthesis, enabling researchers to explore the creation of novel materials and compounds with tailored properties.

The unique combination of the trifluoromethyl group, the quinoline core, and the ethanethiol functionality provides a rich canvas for chemists to paint their innovative designs. By harnessing the reactivity and selectivity of this compound, scientists can unlock new avenues for the development of advanced materials, functional coatings, and a wide array of specialized chemical products.

Technical Specifications and Safety Considerations

2-{[2-(Trifluoromethyl)quinolin-4-yl]amino}ethanethiol boasts a chemical formula of C12H12F3N2S and an MDL number of MFCD11101421. Its HS code, 2933499090, reflects its classification for international trade and regulatory purposes.

While this compound is classified as toxic, proper handling and storage protocols are essential to ensure the safety of researchers and the