1,3,4-Oxathiazole-5-carboxylic acid, 2-oxo-, ethyl ester is a heterocyclic compound characterized by the presence of both sulfur and nitrogen in its ring structure, specifically an oxathiazole ring. This compound features a carboxylic acid functional group that is esterified with an ethyl group, contributing to its solubility and reactivity. The oxathiazole moiety is known for its potential biological activity, making such compounds of interest in medicinal chemistry. The presence of the carbonyl group (2-oxo) enhances its reactivity, allowing for various chemical transformations. Typically, compounds like this may exhibit properties such as antimicrobial or antifungal activity, although specific biological effects would depend on the context of their use and further structural modifications. Additionally, the compound's stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 1,3,4-oxathiazole derivatives are valuable in synthetic organic chemistry and pharmaceutical applications.

1,3,4-OXATHIAZOLE-5-CARBOXYLIC ACID, 2-OXO-, ETHYL ESTER

61689-40-5: 1,3,4-Oxathiazole-5-carboxylic acid, 2-oxo-, ethyl ester is a heterocyclic compound characterized by the presence of both sulfur and nitrogen in its ring structure, specifically an oxathiazole ring. This compound features a carboxylic acid functional group that is esterified with an ethyl group, contributing to its solubility and reactivity. The oxathiazole moiety is known for its potential biological activity, making such compounds of interest in medicinal chemistry. The presence of the carbonyl group (2-oxo) enhances its reactivity, allowing for various chemical transformations. Typically, compounds like this may exhibit properties such as antimicrobial or antifungal activity, although specific biological effects would depend on the context of their use and further structural modifications. Additionally, the compound's stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 1,3,4-oxathiazole derivatives are valuable in synthetic organic chemistry and pharmaceutical applications.

CAS 61689-40-5

1,3,4-OXATHIAZOLE-5-CARBOXYLIC ACID, 2-OXO-, ETHYL ESTER

Ethyl 2-oxo-2H-1,3,4-oxathiazole-5-carboxylate

Ref: 3D-LCA68940