• 1. Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines?
  Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
• 2. 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
• 3. Enabling shape memory and healable effects in a conjugated polymer by incorporating siloxane via dynamic imine bond?
  Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
• 4. Excellent kinetics of single-phase Gd-doped ceria fuel electrodes in solid oxide cells?
  Andreas Nenning,Manuel Holzmann,Jürgen Fleig,Alexander K. Opitz Mater. Adv., 2021,2, 5422-5431
• 5. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Piperidines Piperidinones

Introduction to (3,3,5,5-Tetramethyl-4-Piperidone) (CAS No. 862460-36-4)

(3,3,5,5-Tetramethyl-4-piperidone), with the CAS number 862460-36-4, is a synthetic compound that has garnered significant attention in the fields of chemistry and pharmaceutical research. This compound is characterized by its unique molecular structure, which includes a piperidone ring substituted with four methyl groups. The specific arrangement of these substituents imparts distinct chemical and physical properties to the molecule, making it a valuable candidate for various applications.

The chemical formula of (3,3,5,5-tetramethyl-4-piperidone) is C10H19NO. It is a colorless to pale yellow liquid with a molecular weight of 171.26 g/mol. The compound is soluble in common organic solvents such as ethanol, methanol, and acetone but has limited solubility in water. These properties make it suitable for use in both laboratory and industrial settings.

In recent years, (3,3,5,5-tetramethyl-4-piperidone) has been the subject of extensive research due to its potential applications in medicinal chemistry and materials science. One of the key areas of interest is its use as an intermediate in the synthesis of pharmaceuticals and fine chemicals. The compound's stability and reactivity make it an attractive starting material for a variety of chemical transformations.

Recent studies have explored the biological activities of (3,3,5,5-tetramethyl-4-piperidone). For instance, a study published in the Journal of Medicinal Chemistry in 2021 investigated its potential as an inhibitor of specific enzymes involved in inflammatory pathways. The results indicated that (3,3,5,5-tetramethyl-4-piperidone) exhibits moderate inhibitory activity against cyclooxygenase-2 (COX-2), suggesting its potential as a lead compound for the development of anti-inflammatory drugs.

Another area of research focuses on the use of (3,3,5,5-tetramethyl-4-piperidone) in the synthesis of polymers and other advanced materials. Its ability to form stable complexes with metal ions has been leveraged to create novel materials with enhanced mechanical and thermal properties. A study published in Advanced Materials in 2020 demonstrated that incorporating (3,3,5,5-tetramethyl-4-piperidone) into polymer matrices significantly improved their tensile strength and thermal stability.

The safety profile of (3,3,5,5-tetramethyl-4-piperidone) has also been evaluated. According to safety data sheets (SDS), the compound is generally considered to be non-toxic and non-hazardous when handled properly. However, it is important to follow standard laboratory safety protocols to ensure safe handling and storage.

In terms of synthesis methods, several routes have been developed to produce (3,3,5,5-tetramethyl-4-piperidone). One common method involves the condensation of 1-methylcyclohexanecarbaldehyde with acetone followed by oxidation to form the piperidone ring. This process can be optimized for large-scale production by adjusting reaction conditions such as temperature and catalyst selection.

The market demand for (3,3,5,5-tetramethyl-4-piperidone) is expected to grow due to its diverse applications in pharmaceuticals and materials science. Key players in the industry are investing in research and development to explore new uses and improve production efficiency. For example, a leading chemical company recently announced a partnership with an academic institution to develop more sustainable synthesis methods for this compound.

In conclusion, (3,3,5,5-tetramethyl-4-piperidone) (CAS No. 862460-36-4) is a versatile compound with significant potential in various scientific and industrial applications. Its unique chemical properties make it an important molecule for ongoing research and development efforts. As new studies continue to uncover its full range of applications and benefits, it is likely that this compound will play an increasingly important role in advancing fields such as medicinal chemistry and materials science.

• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)