N-(4-chlorophenyl)-2,2-dimethyl-pentanamide

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Identification

Molecular formula
C13H18ClNO
CAS Number
684-16-4
IUPAC Name
N-(4-chlorophenyl)-2,2-dimethyl-pentanamide
Molecular Weight
241.74g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0800g/cm3
Synonyms
Monalide
Interesting facts

Interesting Facts about N-(4-chlorophenyl)-2,2-dimethyl-pentanamide

N-(4-chlorophenyl)-2,2-dimethyl-pentanamide is a fascinating organic compound with unique properties and applications. Here are some interesting facts about this compound:

  • Functional Groups: This compound contains an amide functional group, which is characterized by a carbonyl (C=O) linked to a nitrogen atom (N). Amides are important in the biological landscape as they are often found in peptides and proteins.
  • Chlorine Atom: The presence of a chlorine atom in the para position of the phenyl ring is significant. Chlorinated compounds often exhibit enhanced pharmacological properties, and chlorine can increase the compound's lipophilicity, impacting its solubility and biological activity.
  • Structure Impact: The bulky 2,2-dimethyl substituents on the pentanamide chain contribute to the compound's steric hindrance, which can affect its reactivity and interactions with other molecules, making it an interesting subject for studies in drug design.
  • Potential Applications: Due to its structure, N-(4-chlorophenyl)-2,2-dimethyl-pentanamide may hold promise in medicinal chemistry. Compounds with similar structures have been explored for their roles in anti-inflammatory and anti-cancer activities.
  • Research Interest: Scientists are continuously investigating the biological significance of amides and their derivatives. This compound serves as a model for studying structure-activity relationships, which aid in the development of new therapeutic agents.

In conclusion, N-(4-chlorophenyl)-2,2-dimethyl-pentanamide represents a valuable compound in both chemical and pharmaceutical research, showcasing the intricate connections between structure and function in organic chemistry.

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