• 1. Fast synthesis of copper nanoclusters through the use of hydrogen peroxide additive and their application for the fluorescence detection of Hg2+ in water samples?
  Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
• 2. 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
• 3. Emerging enantiomeric resolution materials with homochiral nano-fabrications
  Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
• 4. Fe(ii)-Assisted one-pot synthesis of ultra-small core–shell Au–Pt nanoparticles as superior catalysts towards the HER and ORR?
  Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
• 5. Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines?
  Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555

• Solvents and Organic Chemicals Organic Compounds Benzenoids Naphthalenes Naphthalenecarboxylic acids and derivatives

Comprehensive Guide to 1-Naphthalenecarbonylchloride, 4-bromo- (CAS No. 87700-65-0): Properties, Applications, and Industry Insights

1-Naphthalenecarbonylchloride, 4-bromo- (CAS No. 87700-65-0) is a specialized organic compound widely recognized for its role in synthetic chemistry and industrial applications. This halogenated derivative of naphthalene features a bromine substituent at the 4-position and a reactive carbonyl chloride group, making it a versatile intermediate in pharmaceuticals, agrochemicals, and material science. Its molecular formula, C₁₁H₆BrClO, and unique structural properties have garnered significant attention in research and development circles.

In recent years, the demand for 4-bromo-1-naphthalenecarbonyl chloride has surged due to its utility in cross-coupling reactions, a topic frequently searched in AI-driven chemistry platforms. Researchers often inquire about its synthesis methods, purity standards, and handling precautions, reflecting its importance in modern organic synthesis. The compound’s compatibility with palladium-catalyzed reactions (e.g., Suzuki-Miyaura couplings) aligns with the growing interest in sustainable and efficient catalytic processes.

From an industrial perspective, 1-Naphthalenecarbonylchloride, 4-bromo- is pivotal in producing high-performance dyes and liquid crystals, addressing trends in eco-friendly materials and display technologies. Its role in constructing naphthalene-based polymers also resonates with searches for "advanced polymer additives" and "thermal-stable materials." Laboratories prioritize its storage conditions (e.g., moisture-sensitive, inert atmosphere) and analytical characterization (e.g., NMR, HPLC), which are common queries in scientific forums.

Environmental and regulatory considerations further highlight its relevance. While not classified as hazardous under standard guidelines, users often search for "biodegradability of brominated compounds" or "green alternatives to halogenated intermediates," reflecting the industry’s shift toward sustainable chemistry. Innovations in catalytic bromination techniques and waste minimization protocols are frequently discussed in conjunction with this compound.

In summary, 1-Naphthalenecarbonylchloride, 4-bromo- (CAS No. 87700-65-0) bridges academic research and industrial innovation. Its multifaceted applications—from pharmaceuticals to materials science—coupled with evolving synthetic methodologies, ensure its continued prominence in chemical literature and commercial workflows.

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