• 1. An amide probe as a selective Al3+ and Fe3+ sensor inside the HeLa and a549 cell lines: Pictet–Spengler reaction for the rapid detection of tryptophan amino acid?
  Bidyut Kumar Kundu,Rinky Singh,Ritudhwaj Tiwari,Debasis Nayak New J. Chem., 2019,43, 4867-4877
• 2. An intermolecular C–H oxidizing strategy to access highly fused carbazole skeletons from simple naphthylamines?
  Christian K. Rank,Alexander W. Jones,Tatjana Wall,Patrick Di Martino-Fumo,Sarah Schr?ck,Markus Gerhards,Frederic W. Patureau Chem. Commun., 2019,55, 13749-13752
• 3. An insight into the hybridization mechanism of hairpin DNA physically immobilized on chemically modified graphenes
  Adeline Huiling Loo,Alessandra Bonanni,Martin Pumera Analyst, 2013,138, 467-471
• 4. An apparatus for determining small amounts of alchohol in sour milk and urine
  Analyst, 1964,89, 272-275
• 5. An arsenic trioxide nanoparticle prodrug (ATONP) potentiates a therapeutic effect on an aggressive hepatocellular carcinoma model via enhancement of intratumoral arsenic accumulation and disturbance of the tumor microenvironment?
  Xin Fu,Qing-rong Liang,Rong-guang Luo,Yan-shu Li,Xiao-ping Xiao,Lu-lu Yu,Wen-zhe Shan,Guang-qin Fan J. Mater. Chem. B, 2019,7, 3088-3099

• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Ketones
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Carbonyl compounds Ketones

Comprehensive Guide to 4-Ethoxycyclohexanone (CAS No. 23510-92-1): Properties, Applications, and Industry Insights

4-Ethoxycyclohexanone (CAS No. 23510-92-1) is a versatile organic compound widely used in pharmaceutical intermediates, fragrance synthesis, and specialty chemicals. With the growing demand for sustainable and high-performance materials, this ketone derivative has gained attention for its unique structural properties and reactivity. Researchers and manufacturers often search for "4-Ethoxycyclohexanone uses," "CAS 23510-92-1 suppliers," or "synthesis of 4-Ethoxycyclohexanone," reflecting its industrial relevance.

The molecular structure of 4-Ethoxycyclohexanone features a cyclohexanone ring substituted with an ethoxy group at the 4-position, contributing to its moderate polarity and solubility in organic solvents. This characteristic makes it valuable for reactions like Grignard additions or reductive amination, often explored in queries such as "4-Ethoxycyclohexanone reactivity" or "cyclohexanone derivatives in drug discovery." Recent studies highlight its role in green chemistry applications, aligning with trends in eco-friendly synthesis.

In the fragrance industry, 4-Ethoxycyclohexanone serves as a precursor for musk-like odorants, addressing searches like "cyclic ketones in perfumery." Its stability under mild conditions also makes it a candidate for polymer modification, a topic gaining traction in material science forums. Analytical data (e.g., GC-MS, NMR) for CAS 23510-92-1 are frequently requested by QC labs, emphasizing the need for standardized characterization protocols.

Innovations in catalytic hydrogenation have improved the cost-efficiency of producing 4-Ethoxycyclohexanone, reducing environmental impact—a key concern for users searching "sustainable ketone production." Regulatory compliance (e.g., REACH, FDA) for this compound remains straightforward, but manufacturers should monitor updates on "high-purity 4-Ethoxycyclohexanone specifications" to meet evolving industry standards.

Future prospects for 23510-92-1 include potential applications in agrochemicals and liquid crystals, as noted in recent patent filings. For researchers, understanding its "structure-activity relationship" or "scaling up 4-Ethoxycyclohexanone synthesis" could unlock novel functionalities. Collaborative efforts between academia and industry continue to expand its utility beyond traditional domains.

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• 21133-22-2(3-Pentanone, 1,5-bis(tetrahydro-2-furanyl)-)
• 872847-59-1(Cyclohexanone, 3-propoxy-)
• 6624-81-3(1-cyclohexyloxyhexatriacontan-11-one)
• 13619-73-3(Cyclohexanone,3-ethoxy-)
• 155189-69-8(2-Pentanone, 4-ethoxy-,(S)- (9CI))
• 916062-23-2(2-Nonanone, 4-ethoxy-)
• 158836-67-0(4-Propoxycyclohexanone)
• 69697-46-7(4-(propan-2-yloxy)cyclohexan-1-one)
• 652986-75-9(Cyclohexanone, 3-[(1S)-3-hydroxy-1-methylpropoxy]-)