N-(3-amino-4-hydroxyphenyl)sulfanilamide

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Identification

Molecular formula
C13H12N2O5S
CAS Number
59901-73-4
IUPAC Name
2-[(3-amino-4-hydroxy-phenyl)sulfonylamino]benzoic acid
Molecular Weight
292.31g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5676g/cm3
Synonyms
91-35-0
Interesting facts

Interesting Facts About 2-[(3-Amino-4-Hydroxy-Phenyl)Sulfonylamino]Benzoic Acid

This intriguing compound, commonly known in pharmaceutical research, boasts a unique structure that enhances its biological activity. Here are several key insights about it:

  • Pharmaceutical Relevance: This compound is often investigated for its potential as a therapeutic agent due to its ability to interact with various biological targets.
  • Functional Groups: The presence of amino and sulfonamide functional groups contributes to the compound's pharmacological properties, making it an interesting subject for drug design.
  • Structural Diversity: The combination of a benzoic acid moiety with sulfonamide and amino groups showcases the structural diversity observed in medicinal chemistry.
  • Potential Applications: Research indicates that this compound may have applications in treating conditions such as inflammation and cancer, owing to its ability to inhibit key enzymes in disease pathways.

Furthermore, scientists are continuously exploring derivatives of this compound in hopes of enhancing efficacy and reducing side effects. As noted by renowned chemists, "The modification of molecular structures can lead to potential improvements in therapeutic performance." Its rich chemistry not only helps in understanding molecular interactions but also lays the groundwork for the discovery of novel compounds with improved biological functions.

In conclusion, 2-[(3-amino-4-hydroxy-phenyl)sulfonylamino]benzoic acid stands as a promising molecule, reflecting the intricate relationship between chemistry and pharmacology in addressing complex health challenges.

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