• 1. 226. Copper(II) halides as halogenating agents
  D. C. Nonhebel J. Chem. Soc. 1963 1216
• 2. Anion identification using silsesquioxane cages
  Supphachok Chanmungkalakul,Vuthichai Ervithayasuporn,Patcharaporn Boonkitti,Alisa Phuekphong,Nicha Prigyai,Sumana Kladsomboon,Suda Kiatkamjornwong Chem. Sci. 2018 9 7753
• 3. Forced topochemistry of a solid-state Diels–Alder reaction by encapsulation in epoxy glue
  T. A. Lau,S. Khorasani,M. A. Fernandes CrystEngComm 2023 25 3988
• 4. Pincer CNC bis-N-heterocyclic carbenes: robust ligands for palladium-catalysed Suzuki–Miyaura arylation of bromoanthracene and related substrates
  V. M. Zende,C. Schulzke,A. R. Kapdi Org. Chem. Front. 2015 2 1397
• 5. Palladium-catalyzed cyanide metathesis: utilization of benzyl cyanide as an operator-benign reagent for aryl halide cyanations
  Qiaodong Wen,Jisong Jin,Binbin Hu,Ping Lu,Yanguang Wang RSC Adv. 2012 2 6167

• Solvents and Organic Chemicals Organic Compounds Benzenoids Anthracenes Anthracenes
• Solvents and Organic Chemicals Organic Compounds Benzenoids Anthracenes
• Solvents and Organic Chemicals Organic Compounds Organic Halides

Recent Advances in the Application of 9-Bromoanthracene Standard (CAS: 1564-64-3) in Chemical and Biomedical Research

The compound 9-Bromoanthracene (CAS: 1564-64-3) has garnered significant attention in recent years due to its versatile applications in chemical synthesis, material science, and biomedical research. As a standardized reference material, 9-Bromoanthracene Standard is widely utilized in analytical chemistry, particularly in high-performance liquid chromatography (HPLC) and mass spectrometry (MS) for calibration and quality control purposes. This research brief aims to summarize the latest advancements and applications of 9-Bromoanthracene Standard, highlighting its role in contemporary scientific investigations.

Recent studies have demonstrated the utility of 9-Bromoanthracene Standard in the development of novel organic electronic materials. Its unique photophysical properties, including high fluorescence quantum yield and stability, make it an ideal candidate for organic light-emitting diodes (OLEDs) and photovoltaic devices. Researchers have successfully incorporated 9-Bromoanthracene derivatives into polymer matrices to enhance charge transport and luminescence efficiency, paving the way for next-generation optoelectronic applications.

In the realm of biomedical research, 9-Bromoanthracene Standard has been employed as a key intermediate in the synthesis of bioactive molecules. A 2023 study published in the Journal of Medicinal Chemistry reported the use of 9-Bromoanthracene as a precursor for the development of anthracene-based inhibitors targeting specific oncogenic pathways. The study highlighted the compound's ability to modulate protein-protein interactions, offering a promising strategy for cancer therapy. Furthermore, its fluorescence properties have been exploited in bioimaging, enabling real-time tracking of cellular processes.

Analytical applications of 9-Bromoanthracene Standard have also seen notable progress. A recent publication in Analytical Chemistry detailed a novel method for detecting polycyclic aromatic hydrocarbons (PAHs) in environmental samples using 9-Bromoanthracene as an internal standard. The method exhibited superior sensitivity and reproducibility, underscoring the compound's reliability in trace analysis. Additionally, advancements in chromatographic techniques have leveraged 9-Bromoanthracene's retention behavior to optimize separation protocols for complex mixtures.

Despite its widespread use, challenges remain in the large-scale synthesis and purification of 9-Bromoanthracene Standard. Recent efforts have focused on green chemistry approaches to minimize hazardous byproducts and improve yield. A 2024 study in Green Chemistry proposed a solvent-free bromination protocol using mechanochemical methods, which significantly reduced environmental impact while maintaining high purity. These innovations are expected to enhance the accessibility and sustainability of 9-Bromoanthracene Standard for industrial and academic applications.

In conclusion, 9-Bromoanthracene Standard (CAS: 1564-64-3) continues to play a pivotal role in advancing research across multiple disciplines. Its applications in material science, biomedical research, and analytical chemistry underscore its versatility and importance. Future studies are likely to explore its potential in emerging fields such as nanotechnology and drug delivery, further expanding its scientific footprint. Researchers are encouraged to stay abreast of ongoing developments to fully harness the capabilities of this remarkable compound.

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• 21248-00-0(6-Bromobenzo{a}pyrene)
• 83-53-4(1,4-Dibromonaphthalene)
• 27973-29-1(1,6-Dibromopyrene)
• 1732-26-9(4-Bromopyrene)
• 131222-99-6(6,12-Dibromochrysene)
• 3278-82-8(1,5-Dibromoanthracene)
• 1714-29-0(1-Bromopyrene)
• 27497-51-4(Naphthalene,bromo-)