1-(3,5-Dibromophenyl)ethanone (CAS 14401-73-1) is a highly valued intermediate in chemical research due to its versatile reactivity and structural features. Its aryl bromide groups and carbonyl functionality offer numerous avenues for chemical transformations, making it indispensable for synthesizing complex molecules. This article highlights its key applications in various research domains, emphasizing its role as a critical building block.

A Key Intermediate for Advanced Synthesis

Researchers frequently utilize 1-(3,5-Dibromophenyl)ethanone as a starting material for a wide range of synthetic pathways. Its utility spans several critical areas:

  • Pharmaceutical Drug Discovery: The compound is instrumental in constructing heterocyclic rings and functionalized aromatic systems, which are common motifs in many pharmaceutical drugs. Scientists often buy 1-(3,5-Dibromophenyl)ethanone to synthesize novel drug candidates targeting various diseases.
  • Material Science: Its rigid aromatic structure and potential for functionalization make it suitable for creating novel polymers, organic electronic materials, and other advanced materials with tailored properties.
  • Agrochemical Development: Derivatives of 1-(3,5-Dibromophenyl)ethanone can exhibit bioactivity, leading to its application in the synthesis of new pesticides, herbicides, or fungicides.
  • Catalyst Ligand Synthesis: The bromine atoms can be used in palladium-catalyzed cross-coupling reactions to attach phosphine or other coordinating groups, forming ligands for homogeneous catalysis.

As a reputable manufacturer and supplier, we ensure that the 1-(3,5-Dibromophenyl)ethanone we provide has a purity of u226598%, essential for reproducible research outcomes.

Specific Synthetic Transformations

The versatility of 1-(3,5-Dibromophenyl)ethanone is evident in its participation in key reactions such as:

  • Suzuki-Miyaura Coupling: Reacting with boronic acids to form new carbon-carbon bonds, introducing various aryl or vinyl groups.
  • Heck Reaction: Coupling with alkenes to extend carbon chains on the aromatic ring.
  • Grignard Reactions: The carbonyl group can react with Grignard reagents to form tertiary alcohols after further modification.

When seeking to procure this compound for your research, always inquire about the price and availability from reliable suppliers, particularly those specializing in fine chemicals and intermediates. Sourcing from established manufacturers ensures you receive high-quality materials consistently.

Conclusion: Empowering Scientific Advancement

1-(3,5-Dibromophenyl)ethanone is a powerful tool in the arsenal of any research chemist. Its multifaceted applications underscore its importance in driving innovation across pharmaceuticals, materials, and agrochemicals. By partnering with a trusted supplier, researchers can confidently access this crucial intermediate to push the boundaries of scientific discovery.