4-Methoxyacetoacetanilide
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- Molecular formula
- C11H13NO3
- CAS Number
- 556-95-0
- IUPAC Name
- N-(4-methoxyphenyl)-3-oxo-butanamide
- Molecular Weight
- 193.20g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1730g/cm3
- Synonyms
- N-(4-Methoxyphenyl)-3-oxobutanamide
Identification
Interesting facts
Interesting Facts About N-(4-methoxyphenyl)-3-oxo-butanamide
N-(4-methoxyphenyl)-3-oxo-butanamide is a fascinating compound known for its diverse applications in various fields, particularly in medicinal chemistry. Here are some captivating points about this compound:
- Structural Insight: The presence of the methoxy group attached to the phenyl ring contributes to the compound's unique chemical behavior, influencing its reactivity and solubility in organic solvents.
- Biological Activity: Compounds like N-(4-methoxyphenyl)-3-oxo-butanamide have shown potential in pharmaceutical research. Many such amides are being investigated for their anti-inflammatory and analgesic properties.
- Synthesis: The synthesis of this compound often involves multiple steps, typically starting from readily available precursors. The reaction conditions and catalysts play a crucial role in determining the success and efficiency of the synthesis process.
- Importance in Drug Development: The analogs of this compound are of interest in the search for new therapeutic agents. Their ability to modulate biological pathways makes them valuable in drug design.
- Research Applications: Due to its structural features, this compound is often utilized as a building block in the development of more complex molecules in organic synthesis.
Quotes from chemists often highlight the balance of structure and function: “Understanding a compound’s structure can unveil its potential—N-(4-methoxyphenyl)-3-oxo-butanamide is a testament to this notion.”
Overall, N-(4-methoxyphenyl)-3-oxo-butanamide represents a significant focal point in contemporary chemical research, showcasing the intricate relationship between compound structure and biological activity.