Understanding the Chemistry of Ethyl 4-oxocyclohexanecarboxylate for R&D
For research and development scientists, a deep understanding of the chemical behavior of intermediates like Ethyl 4-oxocyclohexanecarboxylate (CAS 17159-79-4) is fundamental to unlocking new synthetic pathways and discovering novel compounds. This molecule, characterized by its cyclic ketone and ester functionalities, offers a versatile platform for a wide array of organic reactions. Knowing its core chemistry helps when you plan to buy and use it effectively.
The reactivity of Ethyl 4-oxocyclohexanecarboxylate is primarily driven by its two key functional groups. The carbonyl group within the cyclohexanone ring is electrophilic, making it susceptible to nucleophilic attack. This allows for reactions such as Grignard additions, Wittig reactions, and reductive aminations, leading to the formation of alcohols, alkenes, and amines, respectively. These transformations are common in the synthesis of complex organic molecules, including those found in pharmaceuticals and agrochemicals.
The ester moiety, specifically the ethoxycarbonyl group, offers further avenues for chemical manipulation. It can undergo hydrolysis to yield the corresponding carboxylic acid, transesterification with other alcohols, or reduction to a primary alcohol using strong reducing agents like lithium aluminum hydride. The interplay between these two functional groups allows for sophisticated synthetic strategies, enabling chemists to build intricate molecular architectures with precision. If your R&D involves such complex synthesis, you’ll want to buy high-purity Ethyl 4-oxocyclohexanecarboxylate.
When sourcing Ethyl 4-oxocyclohexanecarboxylate for research purposes, purity is paramount. A minimum purity of 97% is generally recommended to ensure that side reactions are minimized and experimental results are reproducible. Researchers often look for suppliers who can provide detailed analytical data, such as NMR and GC-MS reports, to confirm the compound's identity and purity. Understanding the price from reputable manufacturers is also key to managing R&D budgets effectively.
In summary, the chemistry of Ethyl 4-oxocyclohexanecarboxylate (CAS 17159-79-4) provides a rich landscape for organic chemists. Its dual functionality makes it a powerful intermediate for creating diverse chemical structures. For scientists engaged in cutting-edge research, identifying reliable suppliers who offer this compound with guaranteed purity at a reasonable price is an essential step towards achieving breakthrough results. We encourage R&D professionals to explore its potential by obtaining a quote from experienced manufacturers.
Perspectives & Insights
Molecule Vision 7
“This molecule, characterized by its cyclic ketone and ester functionalities, offers a versatile platform for a wide array of organic reactions.”
Alpha Origin 24
“The reactivity of Ethyl 4-oxocyclohexanecarboxylate is primarily driven by its two key functional groups.”
Future Analyst X
“The carbonyl group within the cyclohexanone ring is electrophilic, making it susceptible to nucleophilic attack.”