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Comprehensive Guide to 2-Butanone, 4-(4-bromophenyl)- (CAS No. 89201-84-3): Properties, Applications, and Industry Insights

2-Butanone, 4-(4-bromophenyl)- (CAS No. 89201-84-3) is a specialized organic compound that has garnered significant attention in both academic research and industrial applications. This brominated derivative of butanone is characterized by its unique molecular structure, which combines a ketone functional group with a 4-bromophenyl substituent. The presence of the bromine atom enhances the compound's reactivity, making it a valuable intermediate in various synthetic processes. Researchers and industry professionals often search for 2-Butanone, 4-(4-bromophenyl)- uses and 2-Butanone, 4-(4-bromophenyl)- synthesis due to its growing relevance in advanced material science and pharmaceutical development.

The chemical properties of 2-Butanone, 4-(4-bromophenyl)- make it particularly useful in organic synthesis. With a molecular formula of C10H11BrO, this compound exhibits moderate solubility in common organic solvents such as ethanol, acetone, and dichloromethane. Its melting point and boiling point are critical parameters for researchers investigating 2-Butanone, 4-(4-bromophenyl)- reactions or 2-Butanone, 4-(4-bromophenyl)- stability. Recent studies have highlighted its role as a building block for more complex molecules, especially in the development of liquid crystals and photoactive materials. The bromine atom serves as an excellent leaving group in nucleophilic substitution reactions, which is why queries like 2-Butanone, 4-(4-bromophenyl)- reactivity frequently appear in scientific literature searches.

In the pharmaceutical sector, 2-Butanone, 4-(4-bromophenyl)- has emerged as a key intermediate for the synthesis of bioactive molecules. Its structural motif is found in several drug candidates targeting neurological and inflammatory disorders. This connection to healthcare innovations has led to increased searches for 2-Butanone, 4-(4-bromophenyl)- in drug discovery and 2-Butanone, 4-(4-bromophenyl)- medicinal chemistry. The compound's ability to undergo various transformations, including Suzuki-Miyaura cross-coupling reactions, makes it particularly valuable for creating diverse molecular architectures. Pharmaceutical chemists often explore 2-Butanone, 4-(4-bromophenyl)- derivatives to develop novel therapeutic agents with improved efficacy and safety profiles.

The material science community has also recognized the potential of 2-Butanone, 4-(4-bromophenyl)- in advanced applications. Its incorporation into polymer backbones and small-molecule semiconductors has shown promise in organic electronics. Researchers investigating 2-Butanone, 4-(4-bromophenyl)- for OLEDs or 2-Butanone, 4-(4-bromophenyl)- in photovoltaic materials have reported enhanced charge transport properties in derived compounds. This aligns with current industry trends toward sustainable energy solutions and has positioned this chemical as a subject of interest in green chemistry initiatives. The compound's versatility is further demonstrated by its use in creating specialized coatings with unique optical characteristics.

From a commercial perspective, the global market for 2-Butanone, 4-(4-bromophenyl)- has seen steady growth, driven by demand from research institutions and specialty chemical manufacturers. Procurement specialists frequently search for 2-Butanone, 4-(4-bromophenyl)- suppliers and 2-Butanone, 4-(4-bromophenyl)- price trends to secure reliable sources of this valuable intermediate. The compound's niche applications have created opportunities for manufacturers to develop customized purity grades and packaging options to meet diverse customer requirements. Recent advancements in synthetic methodologies have also made production more efficient, addressing queries about 2-Butanone, 4-(4-bromophenyl)- scalable synthesis from process chemistry teams.

Environmental and safety considerations regarding 2-Butanone, 4-(4-bromophenyl)- are important aspects covered in technical documentation. While not classified as highly hazardous, proper handling procedures are recommended, leading to frequent searches for 2-Butanone, 4-(4-bromophenyl)- safety data and 2-Butanone, 4-(4-bromophenyl)- storage conditions. The compound's environmental fate and biodegradation pathways have been studied to ensure compliance with regulatory standards, particularly in regions with stringent chemical management policies. These studies often appear in searches for 2-Butanone, 4-(4-bromophenyl)- ecotoxicity or 2-Butanone, 4-(4-bromophenyl)- regulatory status.

Analytical characterization of 2-Butanone, 4-(4-bromophenyl)- represents another area of significant interest. Quality control laboratories routinely perform analyses using techniques such as HPLC, GC-MS, and NMR spectroscopy, generating searches for 2-Butanone, 4-(4-bromophenyl)- analytical methods and 2-Butanone, 4-(4-bromophenyl)- spectral data. The compound's distinct spectroscopic signatures facilitate its identification in complex mixtures, which is particularly valuable for researchers working on reaction monitoring or impurity profiling. Reference materials and certified standards are available to support these analytical needs, addressing queries about 2-Butanone, 4-(4-bromophenyl)- reference standards from the scientific community.

Looking toward future applications, 2-Butanone, 4-(4-bromophenyl)- continues to attract research attention in emerging fields. Its potential use in metal-organic frameworks (MOFs) and as a ligand precursor in catalysis has opened new avenues for exploration. Scientists investigating 2-Butanone, 4-(4-bromophenyl)- in coordination chemistry or 2-Butanone, 4-(4-bromophenyl)- for advanced materials are contributing to an expanding body of knowledge about this versatile compound. The intersection of synthetic chemistry and materials science promises to unlock additional functionalities that could address current technological challenges in energy storage and conversion.

For researchers and industry professionals seeking detailed technical information, numerous peer-reviewed publications and patents reference 2-Butanone, 4-(4-bromophenyl)-. The compound's presence in scientific literature has grown substantially, with particular emphasis on its role in innovative synthetic strategies. Database searches for 2-Butanone, 4-(4-bromophenyl)- patents or 2-Butanone, 4-(4-bromophenyl)- literature reveal its importance across multiple disciplines. This comprehensive profile underscores the compound's significance in contemporary chemistry and its potential to contribute to future scientific breakthroughs across various technological domains.

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