The Synthetic Utility of 5-Bromoisoquinoline in Chemical Reactions
For chemists and researchers in organic synthesis, understanding the nuanced reactivity of key intermediates is crucial for designing efficient and successful reaction pathways. 5-Bromoisoquinoline (CAS 34784-04-8) is one such compound, offering significant synthetic utility, particularly in areas involving palladium-catalyzed cross-coupling reactions. As a provider of high-quality fine chemicals, we aim to illuminate the importance of this building block for your laboratory.
5-Bromoisoquinoline, presented as a white to yellow-brown crystalline solid, boasts a molecular formula of C9H6BrN and a molecular weight of approximately 208.05 g/mol. Its primary value lies in the presence of the bromine atom, which acts as an excellent leaving group in various transition-metal-catalyzed transformations. This makes it an ideal substrate for reactions such as Suzuki, Sonogashira, Heck, and Buchwald-Hartwig aminations, allowing for the introduction of diverse functional groups onto the isoquinoline core.
The applications of 5-Bromoisoquinoline extend to the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its role as a starting material in palladium-catalyzed aminomethylation and amination reactions is well-documented, enabling the creation of novel nitrogen-containing heterocycles. Researchers looking to buy 5-Bromoisoquinoline can rely on its predictable reactivity to achieve desired molecular architectures.
We are committed to supplying 5-Bromoisoquinoline of high purity, ensuring optimal performance in your synthetic endeavors. If your research requires this essential intermediate, we encourage you to reach out to us. As a dedicated chemical supplier, we offer competitive 5-Bromoisoquinoline pricing and are ready to assist with your inquiries, whether you need small research quantities or larger volumes for scale-up. Explore the synthetic possibilities with our quality intermediates.
Perspectives & Insights
Agile Reader One
“This makes it an ideal substrate for reactions such as Suzuki, Sonogashira, Heck, and Buchwald-Hartwig aminations, allowing for the introduction of diverse functional groups onto the isoquinoline core.”
Logic Vision Labs
“The applications of 5-Bromoisoquinoline extend to the synthesis of pharmaceuticals, agrochemicals, and advanced materials.”
Molecule Origin 88
“Its role as a starting material in palladium-catalyzed aminomethylation and amination reactions is well-documented, enabling the creation of novel nitrogen-containing heterocycles.”