CAS 62305-89-9
:3-Thiomorpholinecarboxylic acid, 5-oxo-, (R)-
Description:
3-Thiomorpholinecarboxylic acid, 5-oxo-, (R)-, with the CAS number 62305-89-9, is a chiral compound that belongs to the class of thiomorpholine derivatives. This substance features a thiomorpholine ring, which is a six-membered heterocyclic structure containing both sulfur and nitrogen atoms. The presence of a carboxylic acid functional group contributes to its acidic properties, while the 5-oxo group indicates the presence of a carbonyl group adjacent to the thiomorpholine ring. The (R)- designation signifies its specific stereochemistry, which can influence its biological activity and interactions. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry and drug development. Its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups. Overall, 3-Thiomorpholinecarboxylic acid, 5-oxo-, (R)- is a notable compound in the realm of organic chemistry, particularly for applications that leverage its unique structural features.
Formula:C5H7NO3S
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Found 7 products.
Cysteine Impurity 1
CAS:Formula:C5H7NO3SColor and Shape:White To Off-White SolidMolecular weight:161.18(R)-5-Oxothiomorpholine-3-carboxylic acid
CAS:<p>(R)-5-Oxothiomorpholine-3-carboxylic acid</p>Purity:97%Molecular weight:161.18g/molLactam of (S)-Carboxymethyl-L-cysteine
CAS:Controlled ProductFormula:C5H7NO3SColor and Shape:NeatMolecular weight:161.179(3R)-5-Oxothiomorpholine-3-carboxylic Acid
CAS:Controlled Product<p>Applications (3R)-5-Oxothiomorpholine-3-carboxylic Acid is used in the synthesis of Mercaptan and dicarboxylate inhibitors of hamster dihydroorotase<br>References Christopherson, R., et al.: Biochemistry., 28, 463-470 (1989)<br></p>Formula:C5H7NO3SColor and Shape:WhiteMolecular weight:161.179(3R)-5-Oxothiomorpholine-3-carboxylic acid
CAS:(3R)-5-Oxothiomorpholine-3-carboxylic acid is a lactam antibiotic that inhibits the growth of bacteria by binding to ribosomes. It acts as an analogue of penicillin, but has a higher affinity for the ribosome. The chemical structure of (3R)-5-oxothiomorpholine-3-carboxylic acid consists of a trifluoroacetate ester at the 3 position, which is responsible for its acidic properties. This drug also contains two functional groups at the 5 position, which are responsible for its ability to interact with sulfoxides and eluting chemicals in chromatography. (3R)-5-Oxothiomorpholine-3-carboxylic acid is used in analytical chemistry as a model for other compounds with similar structures.Formula:C5H7NO3SPurity:Min. 95%Molecular weight:161.18 g/mol







