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N-(4-chlorophenyl)propanamide

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Identification
Molecular formula
C9H10ClNO
CAS number
7529-22-8
IUPAC name
N-(4-chlorophenyl)propanamide
State
State

At room temperature, N-(4-chlorophenyl)propanamide is in a solid state.

Melting point (Celsius)
91.50
Melting point (Kelvin)
364.65
Boiling point (Celsius)
302.10
Boiling point (Kelvin)
575.25
General information
Molecular weight
183.64g/mol
Molar mass
183.6440g/mol
Density
1.2080g/cm3
Appearence

N-(4-chlorophenyl)propanamide appears as a white crystalline solid. The crystals typically have a defined, regular shape typical of many organic compounds.

Comment on solubility

Solubility of N-(4-chlorophenyl)propanamide

N-(4-chlorophenyl)propanamide, a compound characterized by its unique structure, exhibits some interesting solubility properties.

Generally, solubility is influenced by various factors, and for N-(4-chlorophenyl)propanamide, the following aspects are significant:

  • Polarity: The presence of the amide functional group contributes to polarity, which can enhance solubility in polar solvents.
  • Hydrogen bonding: As an amide, N-(4-chlorophenyl)propanamide can engage in hydrogen bonding with solvents, facilitating dissolution.
  • Temperature: Increased temperatures may lead to greater solubility, as higher thermal energy allows more interactions between molecules.
  • Solvent type: This compound is expected to show enhanced solubility in polar protic solvents like water compared to nonpolar solvents like hexane due to its structural features.

However, it is noteworthy that the exact solubility data may vary based on specific conditions such as concentration and specific interactions with solvent molecules. Overall, understanding the solubility of N-(4-chlorophenyl)propanamide is crucial for its applications in chemical processes, where solubility plays a pivotal role in reactivity and product formation.

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.

Synonyms
N-(4-Chlorophenyl)propanamide
4'-CHLOROPROPIONANILIDE
667-891-1
4-Chloropropionanilide
2759-54-8
p-Chloro propion anilide
Propanamide, N-(4-chlorophenyl)-
N-(4-Chlorophenyl)propionamide
NSC-404306
p-Chloropropionanilide
NSC 404306
para-Chloropropionanilide
AI3-17673
4'-chloro-propionanilide
Z99XXJ3NWG
Propionanilide, 4'-chloro-
SCHEMBL4621713
DTXSID40181988
N-(4-Chlorophenyl)propanamide #
NSC404306
AKOS002984600
HS-3361
H20059