N-(4-chlorophenyl)propanamide

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Identification

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
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.

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