Organic Synthesis Building Blocks: Exploring CAS 50342-17-1 Applications
The intricate landscape of organic synthesis relies heavily on versatile building blocks that enable the construction of complex molecular architectures. Among these essential compounds is 1-(4-Bromo-2-hydroxy-5-methylphenyl)ethanone (CAS: 50342-17-1), a compound increasingly recognized for its utility in advanced chemical research and development. As a dedicated manufacturer of high-quality organic intermediates, we are excited to explore the diverse applications that make this molecule a valuable asset for chemists worldwide. Whether you are looking to buy for research or production, understanding its potential is key.
The structure of 1-(4-Bromo-2-hydroxy-5-methylphenyl)ethanone is particularly advantageous for synthetic chemists. It features a phenyl ring substituted with a bromine atom, a hydroxyl group, and a methyl group, alongside an acetyl moiety. This arrangement provides multiple points for functionalization. The bromine atom, for instance, is an excellent leaving group, readily participating in palladium-catalyzed cross-coupling reactions such as Suzuki, Heck, and Sonogashira couplings. These reactions are foundational for forming new carbon-carbon bonds, a critical step in building larger, more complex organic molecules. Researchers seeking to synthesize novel materials or pharmaceutical candidates often leverage these transformations. When you purchase this intermediate, you gain access to a versatile platform for diverse synthetic pathways.
Beyond cross-coupling, the hydroxyl group on the phenyl ring offers another avenue for chemical modification. It can be readily alkylated, acylated, or used in condensation reactions, further expanding the synthetic possibilities. This dual functionality—the reactive bromine and the versatile hydroxyl group—makes 1-(4-Bromo-2-hydroxy-5-methylphenyl)ethanone a sought-after reagent. Its application extends to the synthesis of compounds with potential biological activities. Studies have indicated that derivatives synthesized from this precursor may exhibit antimicrobial or anticancer properties, highlighting its significance in medicinal chemistry research. For those involved in drug discovery, reliable access to such intermediates from a reputable supplier is indispensable.
Furthermore, the acetyl group itself can undergo various transformations, such as reduction to an alcohol or oxidation. This means that the entire molecule can be manipulated in numerous ways, allowing for the precise tailoring of molecular structures. The ability to perform these varied reactions underscores why 1-(4-Bromo-2-hydroxy-5-methylphenyl)ethanone is considered a valuable building block. As a leading manufacturer in China, we ensure that our product maintains high purity standards (97% min.), which is crucial for the success of multi-step syntheses where even trace impurities can significantly impact reaction outcomes and final product quality. Our commitment to quality means you can confidently buy for even the most sensitive organic synthesis projects.
In conclusion, 1-(4-Bromo-2-hydroxy-5-methylphenyl)ethanone (CAS: 50342-17-1) is more than just a chemical compound; it is an enabler of innovation in organic synthesis. Its multifaceted reactivity makes it a crucial component in the creation of pharmaceuticals, advanced materials, and bioactive molecules. For researchers and developers looking to push the boundaries of chemical science, securing a consistent supply of this high-quality intermediate from a trusted manufacturer like us is a strategic first step towards achieving their groundbreaking goals. Explore the possibilities and elevate your synthesis projects with our reliably sourced building blocks.
Perspectives & Insights
Future Origin 2025
“It features a phenyl ring substituted with a bromine atom, a hydroxyl group, and a methyl group, alongside an acetyl moiety.”
Core Analyst 01
“The bromine atom, for instance, is an excellent leaving group, readily participating in palladium-catalyzed cross-coupling reactions such as Suzuki, Heck, and Sonogashira couplings.”
Silicon Seeker One
“These reactions are foundational for forming new carbon-carbon bonds, a critical step in building larger, more complex organic molecules.”