N-(3-chloro-4-cyano-phenyl)acetamide

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Identification

Molecular formula
C9H7ClN2O
CAS Number
94533-56-9
IUPAC Name
N-(3-chloro-4-cyano-phenyl)acetamide
Molecular Weight
194.62g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3240g/cm3
Synonyms
22304-33-2
Interesting facts

Interesting Facts About N-(3-chloro-4-cyano-phenyl)acetamide

N-(3-chloro-4-cyano-phenyl)acetamide is a fascinating compound that plays significant roles in various fields of chemistry and pharmaceuticals. Here are some key points to consider:

  • Pharmaceutical Importance: This compound is often studied for its potential in drug development, particularly in the arena of anti-cancer therapies. Researchers are exploring its effects on tumor growth inhibition.
  • Synthetic Versatility: It's valued for its versatility in organic synthesis, where it can serve as an intermediate in producing other important chemical compounds.
  • Functional Groups: The presence of a cyano group (-C≡N) enhances its reactivity and presents intriguing pathways for chemical modification.
  • Structure-Activity Relationship (SAR): The positioning of the chloro and cyano groups plays a crucial role in determining the biological activity of the molecule, making it a focal point for structure-activity studies.
  • Research Implications: Studies on this compound contribute to our understanding of molecular interactions, which can lead to better therapeutic agents with fewer side effects.

As a compound with unique characteristics, N-(3-chloro-4-cyano-phenyl)acetamide is more than just a simple organic molecule; it embodies the heart of **chemical innovation** and **biological exploration**.

In summary, this compound showcases the intricate relationship between molecular structure and function, making it a subject of ongoing research and discovery in the scientific community.

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