Benzyl 4-Bromophenyl Ether, identified by the CAS number 6793-92-6, is a chemical compound of significant interest due to its versatile applications, particularly as a pharmaceutical intermediate and in organic synthesis. This article explores its fundamental chemical properties, common synthesis routes, and its role in various industrial and research sectors.

Characterized as a white powder, Benzyl 4-Bromophenyl Ether boasts a high purity level, typically exceeding 99%. This purity is critical for its effectiveness in sensitive chemical reactions and pharmaceutical manufacturing processes. The molecule's structure, C13H11BrO, features a benzyl group ether-linked to a 4-bromophenyl group. This structure imparts specific reactivity, making it a valuable building block for constructing more complex organic molecules. Its melting point generally falls within the range of 60-63 °C, and its boiling point is around 340.6 ± 17.0 °C at 760 mmHg, indicating good thermal stability under standard conditions.

The synthesis of Benzyl 4-Bromophenyl Ether often involves the etherification reaction between 4-bromophenol and benzyl halides in the presence of a base. Alternatively, it can be prepared by reacting benzyl alcohol with 4-bromohalobenzenes. These synthetic pathways are well-established, allowing for its efficient production on an industrial scale. The availability of reliable methods to buy Benzyl 4-Bromophenyl Ether online ensures a steady supply for researchers and manufacturers.

The applications of Benzyl 4-Bromophenyl Ether are diverse. As a pharmaceutical intermediate, it is crucial in the synthesis of various APIs, contributing to the development of new drugs for a range of therapeutic areas. Its utility extends to materials science, where it can be incorporated into polymers and other advanced materials to impart specific properties. Furthermore, it serves as a versatile reagent in general organic synthesis, facilitating the creation of complex organic compounds for research and industrial purposes. The consistent quality and high purity of CAS 6793-92-6 are key factors driving its widespread adoption.

Understanding the precise chemical structure and properties of Benzyl 4-Bromophenyl Ether allows chemists to optimize its use in their synthetic strategies. Its role as a reliable chemical building block underscores its importance in advancing scientific research and industrial innovation. Whether for drug development, material creation, or general synthesis, this compound remains a valuable asset in the chemical landscape.