N-(4-chlorophenyl)propanamide
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- Molecular formula
- C9H10ClNO
- CAS Number
- 7529-22-8
- IUPAC Name
- N-(4-chlorophenyl)propanamide
- Molecular Weight
- 183.64g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2080g/cm3
- Synonyms
- N-(4-Chlorophenyl)propanamide
Identification
Interesting facts
Interesting Facts about N-(4-chlorophenyl)propanamide
N-(4-chlorophenyl)propanamide, a compound in the amide class, exhibits fascinating chemical characteristics and applications. Below are some key insights into this intriguing compound:
- Chemical Structure: This compound consists of a propanamide backbone with a 4-chlorophenyl group attached. The presence of the chlorine substitute on the phenyl ring enhances its biological activity, making it a subject of interest in medicinal chemistry.
- Biological Importance: Compounds with similar structures have been studied for their potential use as pharmaceuticals. They may exhibit various biological activities, including antifungal, antibacterial, and anti-inflammatory properties.
- Research Applications: N-(4-chlorophenyl)propanamide can serve as a useful intermediate in organic synthesis, aiding in the development of more complex molecules. Its derivatives are often explored in laboratory settings for drug discovery and chemical innovation.
- Environmental Considerations: Like many chlorinated compounds, the environmental impact of N-(4-chlorophenyl)propanamide is a topic of research. Understanding its degradation products and behavior in ecological systems is crucial for assessing its safety.
- Synthesis: The synthesis of N-(4-chlorophenyl)propanamide typically involves a straightforward reaction between a 4-chlorobenzoic acid derivative and an appropriate amine. This reaction exemplifies key principles of amide formation in organic chemistry.
In conclusion, N-(4-chlorophenyl)propanamide showcases the multifaceted nature of amide compounds. Its unique structural features contribute to its broad chemical applicability and potential in research and industry.