S-Sulfocysteine
- Molecular formula
- C3H6NO5S2Na
- CAS Number
- 15042-96-9
- IUPAC Name
- sodium;(2R)-2-amino-3-sulfosulfanyl-propanoate
- Molecular Weight
- 239.20g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 2.2313g/cm3
Identification
Interesting Facts about Sodium (2R)-2-amino-3-sulfosulfanyl-propanoate
Sodium (2R)-2-amino-3-sulfosulfanyl-propanoate, commonly referred to as a sulfonic acid derivative, is a compound of significant interest in various fields, including biochemistry and pharmaceutical research.
Key Characteristics
- Biological Relevance: This compound serves as a precursor for the synthesis of amino acids and could play a role in metabolic pathways.
- Research Application: It is being explored for its potential therapeutic applications, especially in the treatment of metabolic disorders.
- Unique Functional Group: The sulfonyl group in its structure increases its water solubility and potential reactivity, making it a versatile compound in chemical reactions.
One of the fascinating aspects of sodium (2R)-2-amino-3-sulfosulfanyl-propanoate is its chirality. Being a chiral molecule, it exists in two enantiomeric forms, which can have different biological activities and properties. As highlighted by researchers, "the specificity of enantiomers can lead to varied interactions in biological systems, highlighting the importance of stereochemistry in pharmacology."
Potential Applications
- As an intermediate in the synthesis of more complex bioactive compounds.
- In diagnostics, particularly in the development of assays for amino acid detection.
- In biochemical studies, to explore metabolic pathways involving sulfurs and their derivatives.
In summary, sodium (2R)-2-amino-3-sulfosulfanyl-propanoate is much more than just a simple chemical compound. Its unique properties and potential applications in science and medicine make it a compound worth studying and understanding.