N,N-diethyl-3-oxobutanamide
- Molecular formula
- C8H15NO2
- CAS Number
- 5978-79-0
- IUPAC Name
- N,N-diethyl-3-oxo-butanamide
- Molecular Weight
- 157.21g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 0.9326g/cm3
- Synonyms
- N, N-Diethylacetoacetamide
Identification
Interesting Facts about N,N-Diethyl-3-oxo-butanamide
N,N-Diethyl-3-oxo-butanamide is a fascinating compound that showcases the diversity and complexity of organic chemistry. This compound, belonging to the class of amides, plays a significant role in various industrial and academic applications.
Key Characteristics
- Biological Importance: Compounds like N,N-diethyl-3-oxo-butanamide often serve as substrates in biochemical reactions and can exhibit interesting pharmacological properties that may lead to their use in drug development.
- Synthetic Pathways: The synthesis of such compounds often involves the use of decarboxylation and alkylation reactions, demonstrating the intricate methodologies employed in modern organic synthesis.
- Applications: N,N-diethyl-3-oxo-butanamide can find applications in the synthesis of various other organic molecules, making it a valuable building block in organic chemistry.
Chemical Structure
The compound features a central butanamide backbone, with two ethyl groups enhancing its reactivity and overall properties. This structural arrangement allows for various interactions, including hydrogen bonding and hydrophobic effects, making it an intriguing subject for study in both theoretical and experimental contexts.
Research and Development
As scientists continue to explore the vast realm of organic compounds, N,N-diethyl-3-oxo-butanamide stands out as a compound with potential for new discoveries. Researchers are investigating its properties to understand better its behaviors in different environments and applications.
In summary, N,N-diethyl-3-oxo-butanamide exemplifies the rich tapestry of chemical complexity and serves as a reminder of the endless possibilities present in the world of organic chemistry.