NINGBO INNO PHARMCHEM CO.,LTD. offers an in-depth look at 2-Bromoethyl 4-Nitrophenyl Ether, exploring its fundamental chemical properties and common synthesis methodologies. This compound, identified by CAS Number 13288-06-7, is a vital intermediate widely used in research and industrial applications.

Chemically, 2-Bromoethyl 4-Nitrophenyl Ether is characterized by its molecular formula C8H8BrNO3. It typically presents as a solid, often described as a white powder, with good solubility in organic solvents such as ethanol, chloroform, and dichloromethane. This solubility facilitates its use in solution-phase reactions, which are common in both laboratory synthesis and industrial processes. The presence of a bromine atom on the ethyl chain makes it susceptible to nucleophilic substitution reactions, a key feature exploited in its synthetic applications. Furthermore, the nitro group on the phenyl ring is an electron-withdrawing substituent that influences the reactivity of the aromatic ring and can be chemically transformed, for instance, through reduction to an amino group, opening up further synthetic possibilities.

The synthesis of 2-Bromoethyl 4-Nitrophenyl Ether typically involves reactions that establish the ether linkage and introduce the bromoethyl and nitro functionalities. One common approach involves the Williamson ether synthesis or related ether formation reactions. For example, reacting 4-nitrophenol with a suitable bromoethylating agent, such as 1,2-dibromoethane under basic conditions, can yield the desired product. The exact synthetic route can vary depending on desired purity, yield, and cost-effectiveness, with continuous efforts in process optimization by chemical manufacturers like NINGBO INNO PHARMCHEM CO.,LTD. to ensure high-quality products that meet stringent industry standards. Understanding these properties and synthesis pathways is crucial for anyone working with this important chemical intermediate.