• 1. Emerging investigator series: bacteriophages as nano engineering tools for quality monitoring and pathogen detection in water and wastewater
  Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
• 2. Emerging 2D hybrid nanomaterials: towards enhanced sensitive and selective conductometric gas sensors at room temperature
  Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
• 3. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
  Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
• 4. Evolution and characterization of a benzylguanine-binding RNA aptamer?
  J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
• 5. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693

Comprehensive Overview of Benzene, 1-bromo-2-(2-nitroethyl)- (CAS No. 155988-07-1)

Benzene, 1-bromo-2-(2-nitroethyl)- (CAS No. 155988-07-1) is a specialized organic compound that has garnered significant attention in recent years due to its unique chemical properties and potential applications in various industries. This aromatic derivative, characterized by the presence of a bromo substituent and a nitroethyl group, is a subject of ongoing research in fields such as pharmaceuticals, agrochemicals, and material science. Its molecular structure, C₈H₈BrNO₂, offers a versatile platform for further chemical modifications, making it a valuable intermediate in synthetic chemistry.

The compound's 1-bromo-2-(2-nitroethyl)-benzene nomenclature highlights its functional groups, which are critical for understanding its reactivity and applications. Researchers and industry professionals often search for terms like "synthesis of 1-bromo-2-(2-nitroethyl)-benzene" or "properties of CAS 155988-07-1" to explore its potential. Recent trends in green chemistry have also sparked interest in eco-friendly synthesis methods for this compound, aligning with global sustainability goals. Its role in the development of novel pharmaceutical intermediates and agrochemical precursors further underscores its importance.

One of the key advantages of Benzene, 1-bromo-2-(2-nitroethyl)- is its ability to participate in various chemical reactions, including nucleophilic substitutions and reductions. This versatility makes it a sought-after building block in organic synthesis. For instance, the nitroethyl group can be reduced to an amine, opening pathways to more complex molecules. Meanwhile, the bromo substituent facilitates cross-coupling reactions, which are pivotal in creating advanced materials and bioactive compounds. Such features have led to a surge in queries like "applications of 1-bromo-2-(2-nitroethyl)-benzene" and "CAS 155988-07-1 uses" in academic and industrial circles.

In the context of modern research, Benzene, 1-bromo-2-(2-nitroethyl)- is often discussed alongside emerging technologies such as catalysis and nanomaterials. Its potential role in catalytic processes, particularly in asymmetric synthesis, is a hot topic among chemists. Additionally, the compound's compatibility with polymer chemistry has been explored, with studies focusing on its incorporation into high-performance polymers. These applications align with the growing demand for innovative materials in sectors like electronics and healthcare.

Safety and handling of CAS No. 155988-07-1 are also frequently searched topics. While the compound is not classified as hazardous under standard conditions, proper laboratory practices are essential to ensure safe usage. Researchers often look for guidelines on "storage of 1-bromo-2-(2-nitroethyl)-benzene" and "handling precautions for CAS 155988-07-1" to maintain compliance with safety protocols. This emphasis on safety reflects the broader shift toward responsible chemical management in the scientific community.

Looking ahead, the future of Benzene, 1-bromo-2-(2-nitroethyl)- appears promising, with ongoing studies exploring its potential in drug discovery and material innovation. As the demand for specialized organic intermediates grows, this compound is poised to play a pivotal role in advancing scientific and industrial applications. Its unique combination of reactivity and versatility ensures that it remains a focal point for researchers and industry leaders alike.

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