(3R)-5-oxothiomorpholine-3-carboxylic acid,62305-89-9

1. Physical properties
Chemical formula: C5H7NO3S
Appearance: White crystalline powder or solid
Solubility: Usually has a certain solubility in water, and the solubility is affected by pH value
Melting point: Usually, the melting point ranges around 150°C, but the specific melting point may be affected by different purity and environmental factors
Stability: The compound is stable in a dry environment, but may undergo chemical changes under strong acid or strong base conditions
2. Chemical uses
As a chemical intermediate, 5-oxothiomorpholine-3-carboxylic acid has the following chemical uses:
Biomedical research: Because the compound contains thiol (-SH) and oxo group (C=O), it has certain biological activity. It is often used to synthesize bioactive molecules containing thiol or to study biochemical reactions related to thiol.
Synthetic intermediate: It can be used as an intermediate for the synthesis of other thiol-containing compounds, especially in pharmaceuticals, pesticide chemistry and other organic chemical reactions.
Catalyst or ligand: In some reactions, it may act as a catalyst or ligand to participate in metal-catalyzed reactions, especially in the study of metal complexes.

Drug development: Compounds with thiol structures are often used to develop anticancer, antiviral, antibacterial and other drugs, so this compound has potential in drug design.

Amino acid or peptide synthesis: As an intermediate in organic synthesis, it can be used to synthesize amino acids or peptide chains containing thiol groups.

3. Related reactions
Oxidation reaction: Because its molecules contain thiol groups (-SH), it may participate in redox reactions. Under certain conditions, thiol groups can be oxidized to disulfide bonds (-S-S-) or other oxidation states.

Nucleophilic reaction: The thiol groups may undergo nucleophilic reactions with electrophilic reagents and are widely used in organic synthesis.

Esterification reaction: This compound contains carboxyl groups and can undergo esterification reactions with alcohol compounds to generate corresponding esters.