(4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate

ADVERTISEMENT

Identification

Molecular formula
C19H14N2O6S
CAS Number
50211-17-1
IUPAC Name
(4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate
Molecular Weight
398.41g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3823g/cm3
Synonyms
BRN 3015867
Interesting facts

Exploring (4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate

(4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate is a fascinating chemical compound known for its unique structure and potential applications in various fields. Here are some intriguing aspects of this compound:

  • Chemical Structure: This compound features a complex arrangement of functional groups, including a nitro group and a sulfonyl group. Its dual aromatic rings enhance the molecular stability and reactivity.
  • Applications in Research: As a derivative of carbamates, this compound is of interest in medicinal chemistry. Researchers investigate its role in drug development, particularly in designing inhibitors for specific biological targets.
  • Potential Biological Activity: Compounds like this one often exhibit neuroprotective and anti-inflammatory properties, making them valuable for creating new therapeutic agents.
  • Environmental Implications: The synthesis and degradation of such compounds raise questions in environmental chemistry, as some carbamate derivatives can impact ecosystems. Understanding their behavior is crucial.
  • Research Trends: There is a growing trend towards creating derivatives of carbamates with enhanced selectivity and activity. This compound serves as a benchmark for synthesizing novel agents with improved pharmacological profiles.

In summary, (4-nitrophenyl) N-[4-(benzenesulfonyl)phenyl]carbamate exemplifies the intricate relationship between structure and function in chemistry. The study of such compounds not only deepens our understanding of chemical interactions but also opens new avenues in drug discovery and environmental stewardship.

ADVERTISEMENT