• 1. Fe3O4 nanosphere@microporous organic networks: enhanced anode performances in lithium ion batteries through carbonization?
  Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
• 2. Fe3O4@PANI: a magnetic polyaniline nanomaterial for highly efficient and handy enrichment of intact N-glycopeptides??
  Zhizhen Lai,Mo Zhang,Jinyu Zhou,Tianjing Chen,Dan Li,Xuejing Shen,Jia Liu,Jiang Zhou,Zhili Li Analyst, 2021,146, 4261-4267
• 3. Fe3O4/PEG-SO3H as a heterogeneous and magnetically-recyclable nanocatalyst for the oxidation of sulfides to sulfones or sulfoxides
  Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
• 4. Exciplex emission from the mixed dimer of naphthalene and 2-cyanonaphthalene in a supersonic jet
  Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
• 5. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?
  Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293

• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Aminophenyl ethers

Comprehensive Guide to 4-(Cyclohexyloxy)aniline (CAS No. 39905-48-1): Properties, Applications, and Industry Insights

4-(Cyclohexyloxy)aniline (CAS No. 39905-48-1) is a specialized organic compound widely recognized for its versatile applications in pharmaceuticals, agrochemicals, and material science. This aromatic amine, featuring a cyclohexyloxy substituent, has garnered significant attention due to its unique chemical properties and potential in synthetic chemistry. Researchers and industry professionals often search for terms like "4-(Cyclohexyloxy)aniline synthesis", "CAS 39905-48-1 uses", or "cyclohexyloxy aniline derivatives" to explore its capabilities.

The molecular structure of 4-(Cyclohexyloxy)aniline combines an aniline moiety with a cyclohexyl ether group, offering both lipophilic and electron-donating characteristics. This duality makes it valuable in designing drug intermediates, where solubility and reactivity are critical. Recent trends highlight its role in developing non-steroidal anti-inflammatory drugs (NSAIDs) and antioxidant agents, aligning with the growing demand for sustainable healthcare solutions. Searches for "bioactive aniline compounds" or "pharmaceutical intermediates 2024" reflect this interest.

In material science, CAS 39905-48-1 serves as a precursor for advanced polymers and coatings. Its ability to form stable covalent bonds with epoxy resins or polyurethanes has led to innovations in high-performance adhesives and UV-resistant materials. Industry forums frequently discuss queries such as "aniline-based polymer modifications" or "cyclohexyloxy group in material stability", underscoring its technical relevance.

Environmental and regulatory considerations are also pivotal. While 4-(Cyclohexyloxy)aniline is not classified as hazardous under major chemical inventories, its handling requires standard organic lab protocols. Eco-conscious manufacturers often explore "green synthesis of aniline derivatives" or "biodegradable amine compounds", driving research toward safer production methods.

Analytical techniques like HPLC, GC-MS, and NMR are essential for characterizing 39905-48-1 purity, a topic frequently searched alongside "analytical methods for aromatic amines". The compound’s stability under varying pH and temperature conditions further supports its industrial adoption.

Looking ahead, 4-(Cyclohexyloxy)aniline is poised to play a key role in smart materials and targeted drug delivery systems. As synthetic chemistry evolves, this compound’s adaptability ensures its prominence in answering modern scientific challenges.

• 138859-29-7(4-(1-methylbutoxy)aniline hydrochloride)
• 56714-25-1(Benzenamine,4-(bicyclo[2.2.2]oct-1-yloxy)-)
• 87991-66-0(Benzenamine, 4-(2-cyclohexyl-1,1-dimethylethoxy)-)
• 26455-36-7(4-(Cyclopentyloxy)aniline)
• 88132-46-1(Benzenamine, 4-(2-cyclohexyl-1-methylethoxy)-)
• 179598-09-5(Benzenamine, 4-[[(1S)-1-methylheptyl]oxy]-)
• 105971-50-4(4-(Cyclohexyloxy)aniline hydrochloride)
• 90076-88-3(Benzenamine,4,4'-[1,8-octanediylbis(oxy)]bis- (9CI))
• 89264-49-3(1,2-Benzenediamine, 4-(cyclohexyloxy)-)
• 1172521-22-0(4-(cyclopentyloxy)aniline hydrochloride)