• 1. Establishing empirical design rules of nucleic acid templates for the synthesis of silver nanoclusters with tunable photoluminescence and functionalities towards targeted bioimaging applications?
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• 2. Emulsion soft templating of carbide-derived carbon nanospheres with controllable porosity for capacitive electrochemical energy storage?
  M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
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• 4. Excited state dynamics of symmetric and asymmetric Cr3(dpa)4Cl2 measured using femtosecond transient absorption spectroscopy?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Biphenyls and derivatives Brominated biphenyls

Comprehensive Overview of [1,1'-Biphenyl]-4-ol,2-bromo- (CAS No. 15460-07-8): Properties, Applications, and Industry Insights

[1,1'-Biphenyl]-4-ol,2-bromo- (CAS No. 15460-07-8) is a halogenated biphenyl derivative that has garnered significant attention in pharmaceutical and material science research. This compound, characterized by its brominated aromatic structure, serves as a versatile intermediate in organic synthesis. Its molecular formula, C₁₂H₉BrO, combines a biphenyl backbone with a hydroxyl group and a bromine substituent, enabling unique reactivity patterns. Researchers frequently explore its role in cross-coupling reactions, a topic trending in green chemistry discussions due to the demand for sustainable synthetic methods.

The compound's physicochemical properties include a molecular weight of 249.10 g/mol and a melting point range of 120–125°C, making it suitable for controlled reactions under mild conditions. Recent studies highlight its utility in OLED materials, aligning with the surge in interest around flexible electronics and energy-efficient displays. A 2023 Journal of Materials Chemistry review emphasized its potential as an electron-transport layer component, addressing FAQs about "organic semiconductor alternatives" in search engine queries.

In pharmaceutical contexts, [1,1'-Biphenyl]-4-ol,2-bromo- acts as a precursor for biaryl ether scaffolds, pivotal in designing kinase inhibitors. This resonates with the growing focus on targeted cancer therapies, a frequently searched topic in AI-driven drug discovery platforms. Analytical techniques like HPLC (≥98% purity) and NMR spectroscopy ensure its quality, addressing lab professionals' concerns about "halogenated compound characterization"—a top search phrase in academic forums.

Environmental considerations are critical when handling brominated compounds. While not classified as hazardous under standard regulations, its degradation pathways are studied in bioremediation research, tapping into the eco-conscious trend. Industry reports suggest a 15% annual growth in demand for such intermediates, driven by agrochemical innovations and liquid crystal formulations—key areas where users seek "specialty chemical suppliers" online.

Storage recommendations include amber vials at 2–8°C to prevent photodegradation, a detail often queried by procurement specialists. The compound's chromatographic behavior (logP ≈3.2) also makes it relevant to QSAR modeling discussions, a hot topic in computational chemistry circles. Patent analyses reveal over 50 applications since 2020, particularly in photoresist technologies for microelectronics, answering niche searches like "high-refractive-index polymers".

Emerging applications in metal-organic frameworks (MOFs) further position CAS No. 15460-07-8 as a material of interest for gas storage solutions—a trending subject in clean energy debates. Suppliers increasingly highlight its scalable synthesis routes, responding to manufacturer inquiries about "batch-to-batch consistency" in specialty chemicals. As regulatory landscapes evolve, its REACH compliance status remains updated, addressing EU market access concerns.

• 116087-13-9(3,5-dibromo-4-(4-hydroxy-3,5-dimethylphenyl)-2,6-dimethylphenol)
• 60710-39-6(3-Bromo-4-methylphenol)
• 62388-10-7([1,1'-Biphenyl]ol, bromo-)
• 29558-77-8(4-Bromo-4'-hydroxybiphenyl)
• 14957-65-4([1,1'-Biphenyl]-2,2'-diol,4,4',6,6'-tetrabromo-)
• 70066-66-9(4-(2-Bromophenyl)phenol)
• 84530-63-2(1,1'-Biphenyl, 2,2'-dibromo-4,4'-dimethoxy-)
• 13979-81-2(3,5-Dibromo-4-methylphenol)
• 40976-67-8([1,1'-Biphenyl]-4,4'-diol, 2,2',6,6'-tetrabromo-3,3',5,5'-tetramethyl-)
• 74447-76-0(1-(2-Bromophenyl)-4-methoxybenzene)