4-Ethyl-4-methylpiperidine-2,6-dione
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- Molecular formula
- C8H13NO2
- CAS Number
- 933-08-8
- IUPAC Name
- 4-ethyl-4-methyl-piperidine-2,6-dione
- Molecular Weight
- 155.21g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1537g/cm3
- Synonyms
- bemegride
Identification
Interesting facts
Interesting Facts about 4-Ethyl-4-Methyl-Piperidine-2,6-Dione
4-Ethyl-4-methyl-piperidine-2,6-dione is a fascinating compound that falls under the category of piperidine derivatives. This compound is notable for its unique structural features, which lend it a variety of properties and potential applications. Here are some compelling aspects to consider:
- Structure and Stability: The piperidine ring structure provides this compound with a stable framework. The presence of both the ethyl and methyl groups makes it a substituted derivative, enhancing its chemical reactivity.
- Medical Applications: Due to its piperidine core, compounds like 4-ethyl-4-methyl-piperidine-2,6-dione are often studied for their potential pharmacological properties. Piperidine derivatives have been used in the design of various pharmaceuticals.
- Reactivity: The diketone functionality in this compound can participate in nucleophilic addition reactions, making it useful in the synthesis of more complex organic molecules.
- Synthetic Routes: The preparation of piperidine derivatives often involves several synthetic methodologies, including cyclization reactions. This can make the synthesis of 4-ethyl-4-methyl-piperidine-2,6-dione a subject of interest for organic chemists.
- Research Potential: The exploration of 4-ethyl-4-methyl-piperidine-2,6-dione in medicinal chemistry is ongoing. Its unique structure may lead to the discovery of novel therapeutic agents.
In summary, 4-ethyl-4-methyl-piperidine-2,6-dione is not just a simple compound; it represents a gateway to further exploration in organic synthesis and medicinal chemistry. The compound exemplifies the significance of piperidine derivatives in modern drug development and research.