4-Amino-2-mercaptobenzoic acid

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Identification

Molecular formula
C7H7NO2S
CAS Number
137-14-6
IUPAC Name
4-amino-2-sulfanyl-benzoic acid
Molecular Weight
169.19g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5120g/cm3
Synonyms
4-amino-2-sulfanylbenzoic acid
Interesting facts

Exploring 4-amino-2-sulfanyl-benzoic acid

4-amino-2-sulfanyl-benzoic acid, often abbreviated as ASBA, is a fascinating example of an aromatic amino acid derivative. This compound is notable for its diverse applications and interesting chemical properties, making it a subject of study in both organic chemistry and medicinal research.

Key Characteristics

  • Aromatic Structure: The presence of a benzene ring lends this compound unique stability and reactivity, valued in various synthesis processes.
  • Amino Group: The amino group (-NH2) is crucial for its role in forming peptide bonds, which are fundamental to proteins.
  • Thiol Group: The sulfanyl (or thiol) group (-SH) enhances its potential for biochemical interactions, making it important for enzyme activity.

Applications in Science

This compound has garnered attention in several fields:

  • Pharmaceuticals: 4-amino-2-sulfanyl-benzoic acid has potential applications in drug development, especially in creating compounds that target specific biological mechanisms.
  • Biochemistry: Its ability to interact with certain enzymes positions it as a candidate for research in metabolic pathways.
  • Analytical Chemistry: ASBA can serve as a reagent in various analytical techniques, offering insights into both organic and inorganic substances.

Interesting Quote

As one scientist put it, "The interplay of the functional groups in 4-amino-2-sulfanyl-benzoic acid opens up pathways for innovative drug design." This speaks to the compound's importance in the frontier of chemical research.

Overall, 4-amino-2-sulfanyl-benzoic acid stands as a compelling compound with a rich chemical profile and a range of applications that continue to inspire researchers and scientists alike.

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