• 1. An artificial CO-releasing metalloprotein built by histidine-selective metallation?
  Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
• 2. An integrated process of CO2 capture and in situ hydrogenation to formate using a tunable ethoxyl-functionalized amidine and Rh/bisphosphine system?
  Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
• 3. An alternative biorefinery approach to address microalgal seasonality: blending with spent coffee grounds
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• 4. An atomically efficient, highly stable and redox active Ce0.5Tb0.5Ox (3% mol.)/MgO catalyst for total oxidation of methane?
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• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Diarylethers
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Ethers Diarylethers

Comprehensive Overview of 6-(4-Chlorophenoxy)pyridine-3-carbaldehyde (CAS No. 1160430-66-9)

6-(4-Chlorophenoxy)pyridine-3-carbaldehyde (CAS No. 1160430-66-9) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This pyridine derivative features a 4-chlorophenoxy substituent and an aldehyde functional group, making it a versatile intermediate for synthesizing more complex molecules. Researchers and industries are increasingly exploring its potential due to its unique structural properties and reactivity.

The compound's molecular formula is C₁₂H₈ClNO₂, with a molecular weight of 233.65 g/mol. Its chemical structure combines a pyridine ring with a chlorophenoxy group, which enhances its applicability in drug discovery and material science. Recent studies highlight its role in developing antimicrobial agents and catalytic processes, aligning with the growing demand for innovative solutions in healthcare and sustainable chemistry.

One of the most searched questions about 6-(4-Chlorophenoxy)pyridine-3-carbaldehyde revolves around its synthesis methods. The compound is typically prepared through cross-coupling reactions or oxidation of pyridine alcohols, with researchers optimizing yields and purity for industrial-scale production. Its aldehyde group offers a reactive site for further functionalization, making it a valuable building block in organic synthesis.

In the context of green chemistry, 6-(4-Chlorophenoxy)pyridine-3-carbaldehyde has been investigated for its potential in biodegradable materials and eco-friendly catalysts. This aligns with global trends toward sustainable practices, as industries seek alternatives to traditional petrochemical-derived intermediates. Its low toxicity profile and high stability further enhance its appeal for environmentally conscious applications.

Another hot topic is the compound's role in pharmaceutical intermediates. With the rise of precision medicine and targeted therapies, 6-(4-Chlorophenoxy)pyridine-3-carbaldehyde is being explored for its ability to modify bioactive molecules. Its chlorophenoxy moiety is particularly noteworthy, as it can influence the pharmacokinetic properties of drug candidates, improving their efficacy and safety profiles.

From a commercial perspective, the demand for 6-(4-Chlorophenoxy)pyridine-3-carbaldehyde is driven by its utility in high-value chemical production. Suppliers and manufacturers are increasingly listing this compound in catalogs, catering to the needs of research institutions and industrial laboratories. Quality control measures, such as HPLC analysis and spectroscopic characterization, ensure its suitability for advanced applications.

In summary, 6-(4-Chlorophenoxy)pyridine-3-carbaldehyde (CAS No. 1160430-66-9) represents a critical intermediate in modern chemistry. Its multifaceted applications—from drug development to sustainable materials—underscore its importance in addressing contemporary scientific and industrial challenges. As research progresses, this compound is poised to play an even greater role in innovation across multiple sectors.

• 51362-37-9(2-(4-chlorophenoxy)nicotinic acid)
• 106341-46-2(Pyridine, 5-(chloromethyl)-2-(4-chlorophenoxy)-)
• 173282-69-4(6-Phenoxynicotinaldehyde)
• 459819-79-5(4-[(5-Chloro-2-pyridinyl)oxy]Benzaldehyde)
• 1160430-65-8(3-Pyridinecarboxaldehyde, 6-(3,4-dichlorophenoxy)-)
• 1160430-68-1(3-Pyridinecarboxaldehyde, 6-(4-methoxyphenoxy)-)
• 728934-83-6(Benzaldehyde, 3-[(5-chloro-2-pyridinyl)oxy]-)
• 1160430-78-3(6-(4-Chlorophenoxy)pyridin-3-ylmethanol)
• 478031-03-7(2-(4-chlorophenoxy)nicotinaldehyde)
• 338960-65-9(6-(4-methylphenoxy)pyridine-3-carbaldehyde)