N-(4-chlorophenyl)benzenesulfonamide
- Molecular formula
- C12H10ClNO2S
- CAS Number
- 35303-76-5
- IUPAC Name
- N-(4-chlorophenyl)benzenesulfonamide
- Molecular Weight
- 281.73g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4370g/cm3
- Synonyms
- N-(4-CHLOROPHENYL)BENZENESULFONAMIDE
Identification
Interesting Facts about N-(4-chlorophenyl)benzenesulfonamide
N-(4-chlorophenyl)benzenesulfonamide, widely studied for its potential therapeutic applications, represents a fascinating class of chemical compounds known as sulfonamides. These compounds have a unique structure that contributes to their diverse biological activities.
Key Features
- Antimicrobial Properties: Many sulfonamides, including this one, have been explored for their antimicrobial effects, providing a base for the development of antibiotics.
- Role in Drug Development: Due to their chemical versatility, sulfonamides have been pivotal in medicinal chemistry, leading to the synthesis of numerous pharmaceutical agents.
- Biochemical Mechanism: The sulfonamide group can mimic p-aminobenzoic acid (PABA), inhibiting bacterial folate synthesis, which is vital for DNA and RNA production.
Applications
- Current research is examining N-(4-chlorophenyl)benzenesulfonamide's role in treating bacterial infections.
- There is ongoing interest in its antitumor properties, with studies exploring its effectiveness against certain types of cancer cells.
- Its use as a building block in organic synthesis opens doors for developing novel compounds in various fields.
Please note: While investigating this compound, researchers must pay attention to potential side effects such as hypersensitivity reactions, which highlight the importance of thorough pharmacological evaluations.
In Conclusion
The importance of N-(4-chlorophenyl)benzenesulfonamide in both research and application cannot be overstated. Its impact resonates across multiple fields including pharmaceuticals, biochemistry, and synthetic organic chemistry, making it a compound of great interest in scientific explorations.