Sulfathiazole
- Molecular formula
- C9H9N3O2S2
- CAS Number
- 72-14-0
- IUPAC Name
- 4-amino-N-thiazol-2-yl-benzenesulfonamide
- Molecular Weight
- 255.31g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5400g/cm3
- Synonyms
- sulfathiazole
Identification
Interesting Facts about 4-amino-N-thiazol-2-yl-benzenesulfonamide
4-amino-N-thiazol-2-yl-benzenesulfonamide, often referred to in scientific literature as a compound with significant pharmaceutical implications, is a fascinating example of how small changes in molecular structure can lead to major differences in biological activity. Here are some key insights:
- Pharmaceutical Applications: This compound belongs to a class of molecules with potential use as antibacterial agents. Its unique structure allows it to inhibit bacterial growth, which is crucial in the development of new antibiotics.
- Thiazole Ring Benefits: The thiazole moiety in its structure has been extensively studied for its role in medicinal chemistry. It enhances the compound's interaction with biological targets, leading to higher efficacy in treatments.
- Dual Functionality: 4-amino-N-thiazol-2-yl-benzenesulfonamide showcases not only antibacterial properties but may also possess antivirulent characteristics. This dual functionality opens new avenues in infectious disease management.
- Sulfonamide Derivative: As a derivative of sulfonamides, this compound contributes to the ongoing exploration of sulfa drugs, which were among the first antibiotics ever developed. The persistence of sulfonamides in modern medicine is a testament to their significance.
In summary, the exploration of compounds like 4-amino-N-thiazol-2-yl-benzenesulfonamide is critical for the future of drug development. As chemists continue to uncover the mechanisms of action and optimize structure-activity relationships, this compound could play a vital role in combating resistant strains of bacteria. "The molecular diversity in medicinal compounds opens infinite possibilities for innovation."