4-Amino-2-mercaptobenzoic acid
- 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
Identification
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.