Boost Your Synthesis: Why 4-Bromo-2-(trifluoromethyl)benzonitrile is Key
In the intricate world of organic chemistry, the selection of high-quality intermediates is paramount to successful synthesis. One such versatile compound that has garnered significant attention is 4-Bromo-2-(trifluoromethyl)benzonitrile, identified by its CAS number 191165-13-6. As a leading manufacturer and supplier based in China, we are proud to offer this critical chemical building block to researchers and industrial chemists worldwide. Understanding its properties and applications can significantly enhance your synthetic strategies.
The structure of 4-Bromo-2-(trifluoromethyl)benzonitrile is characterized by a benzonitrile core, substituted with a bromine atom and a trifluoromethyl group. This unique combination of functional groups makes it an invaluable precursor in a multitude of organic reactions. Its primary utility lies in its role as an intermediate for the synthesis of 4-Bromo-2-(trifluoromethyl)phenylacetic Acid, a compound that itself serves as a stepping stone in the creation of more complex molecules. This pathway is particularly relevant in the pharmaceutical industry, where precise molecular architecture is essential for drug efficacy.
For procurement professionals and R&D scientists, the decision to buy this intermediate hinges on factors like purity, availability, and cost. We address these concerns by ensuring a high purity level, typically above 98%, which is crucial for predictable reaction outcomes and minimizing side products. Our strategic location in China allows us to offer competitive pricing, making it feasible for both small-scale research projects and large-scale industrial production to access this vital chemical.
Beyond its direct application in phenylacetic acid synthesis, 4-Bromo-2-(trifluoromethyl)benzonitrile can be employed in various cross-coupling reactions, nucleophilic substitutions, and other transformations. The presence of the bromine atom makes it a prime candidate for palladium-catalyzed coupling reactions, such as Suzuki, Heck, and Sonogashira couplings, allowing for the introduction of diverse aryl, alkenyl, or alkynyl groups. The trifluoromethyl group, known for its electron-withdrawing nature and lipophilicity, can impart desirable properties to the final molecules, including enhanced metabolic stability and bioavailability, which are highly sought after in drug discovery.
When considering where to purchase this chemical, choosing a reliable manufacturer is key. We pride ourselves on not only the quality of our products but also on our commitment to customer service and supply chain stability. Our production processes are optimized for efficiency and environmental responsibility, ensuring a consistent and dependable supply. If you are looking to integrate 4-Bromo-2-(trifluoromethyl)benzonitrile into your synthesis workflow, we encourage you to request a quote and sample. Our team is ready to assist you in securing the materials needed to drive your innovation forward.
Perspectives & Insights
Future Origin 2025
"We pride ourselves on not only the quality of our products but also on our commitment to customer service and supply chain stability."
Core Analyst 01
"Our production processes are optimized for efficiency and environmental responsibility, ensuring a consistent and dependable supply."
Silicon Seeker One
"If you are looking to integrate 4-Bromo-2-(trifluoromethyl)benzonitrile into your synthesis workflow, we encourage you to request a quote and sample."