N,N-Dimethyl-4-(trichloroacetyl)benzenesulfonamide

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Identification

Molecular formula
C10H11Cl3NO2S
CAS Number
101-20-2
IUPAC Name
2,2,2-trichloro-N-[4-(dimethylsulfamoyl)phenyl]acetamide
Molecular Weight
296.64g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.6200g/cm3
Synonyms
23280-37-7
Interesting facts

Interesting Facts about 2,2,2-Trichloro-N-[4-(dimethylsulfamoyl)phenyl]acetamide

This compound, known as a derivative of acetaminophen, plays a significant role in the field of medicinal chemistry. Here are some fascinating insights:

  • Medicinal Applications: It has been studied for its potential use in anti-inflammatory and analgesic properties, making it a candidate for pain relief research.
  • Unique Structure: The presence of three chlorine atoms contributes to its enhanced reactivity, which is crucial for its biological activity.
  • Sulfamoyl Group: The dimethylsulfamoyl moiety impacts the compound's pharmacological properties, potentially improving solubility and bioavailability.
  • Research Relevance: Due to its complex structure, it serves as a valuable model for developing new therapies targeting various diseases.
  • Safety Considerations: As with many halogenated compounds, careful attention is needed for handling and disposal due to potential toxicity.

In the realm of chemical research, compounds like 2,2,2-trichloro-N-[4-(dimethylsulfamoyl)phenyl]acetamide highlight the intricate interplay between structure and function, paving the way for innovative drug development. As we delve deeper into its mechanism of action, we may uncover novel approaches for combating pain and inflammation.

Remember, in the world of chemistry, every compound has the potential to reveal new therapeutic pathways, making it an exciting field of study!

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