• 1. An alumina stabilized graphene oxide wrapped SnO2 hollow sphere LIB anode with improved lithium storage?
  Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
• 2. An intensified π-hole in beryllium-doped boron nitride meshes: its determinant role in CO2 conversion into hydrocarbon fuels?
  Luis Miguel Azofra,Douglas R. MacFarlane,Chenghua Sun Chem. Commun., 2016,52, 3548-3551
• 3. An amorphous carbon nitride/NiO/CoN-based composite: a highly efficient nonprecious electrode for supercapacitors and the oxygen evolution reaction?
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• 4. An anti-ultrasonic-stripping effect in confined micro/nanoscale cavities and its applications for efficient multiscale metallic patterning?
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• 5. An insight into the origin of room-temperature ferromagnetism in SnO2 and Mn-doped SnO2 quantum dots: an experimental and DFT approach?
  Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514

• Solvents and Organic Chemicals Organic Compounds Benzenoids Naphthalenes Naphthols and derivatives

Comprehensive Analysis of 8-Bromonaphthalen-1-ol (CAS No. 62456-32-0): Properties, Applications, and Industry Insights

8-Bromonaphthalen-1-ol (CAS No. 62456-32-0) is a halogenated naphthalene derivative widely recognized for its versatile applications in organic synthesis, pharmaceuticals, and material science. This compound, characterized by a bromine substituent at the 8-position and a hydroxyl group at the 1-position of the naphthalene ring, exhibits unique chemical properties that make it valuable for researchers and industrial applications. With the growing demand for halogenated aromatic compounds in drug discovery and advanced materials, 8-Bromonaphthalen-1-ol has garnered significant attention in recent years.

The molecular structure of 8-Bromonaphthalen-1-ol (C₁₀H₇BrO) combines the stability of naphthalene with the reactivity of bromine and hydroxyl functional groups. This dual functionality enables its use as a building block in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, which are pivotal in creating complex organic molecules. Researchers frequently search for "8-Bromonaphthalen-1-ol synthesis" or "CAS 62456-32-0 applications," reflecting its importance in modern synthetic chemistry.

In the pharmaceutical sector, 8-Bromonaphthalen-1-ol serves as a precursor for developing bioactive molecules and fluorescent probes. Its bromine atom allows for further functionalization, making it a key intermediate in designing targeted therapies. Recent studies highlight its potential in cancer research and neurodegenerative disease studies, aligning with trending topics like "halogenated drug intermediates" and "small-molecule therapeutics."

Material scientists leverage 8-Bromonaphthalen-1-ol to develop organic semiconductors and luminescent materials. Its naphthalene core contributes to π-conjugation, essential for optoelectronic devices such as OLEDs and solar cells. Queries like "naphthalene derivatives for OLEDs" or "CAS 62456-32-0 in material science" underscore its relevance in sustainable technology innovations.

Environmental and safety considerations are critical when handling 8-Bromonaphthalen-1-ol. While not classified as hazardous under standard conditions, proper storage (away from light and moisture) and handling protocols are recommended. This aligns with the increasing focus on "green chemistry alternatives" and "sustainable chemical synthesis," which dominate current industry discussions.

In summary, 8-Bromonaphthalen-1-ol (CAS No. 62456-32-0) bridges multiple scientific disciplines, from medicinal chemistry to advanced materials engineering. Its adaptability to diverse reactions and applications ensures its continued prominence in research and industrial workflows. For those exploring "buy 8-Bromonaphthalen-1-ol" or "technical specifications of CAS 62456-32-0," understanding its multifaceted roles is essential for optimizing its use in cutting-edge innovations.

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