Ethyl 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylate, with the CAS number 3354-38-9, is a chemical compound characterized by its unique structure that includes a dithiole ring, which is a five-membered heterocyclic compound containing two sulfur atoms. This compound features an amino group and a carboxylate ester, contributing to its reactivity and potential biological activity. The thioxo group indicates the presence of a sulfur atom double-bonded to a carbon atom, which can influence the compound's chemical properties and interactions. Ethyl 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylate is often studied for its potential applications in medicinal chemistry and as a building block in organic synthesis. Its properties may include solubility in organic solvents, moderate stability under standard conditions, and the ability to participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions. Overall, this compound represents an interesting subject for research due to its structural features and potential utility in various chemical applications.

ethyl 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylate

3354-38-9: Ethyl 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylate, with the CAS number 3354-38-9, is a chemical compound characterized by its unique structure that includes a dithiole ring, which is a five-membered heterocyclic compound containing two sulfur atoms. This compound features an amino group and a carboxylate ester, contributing to its reactivity and potential biological activity. The thioxo group indicates the presence of a sulfur atom double-bonded to a carbon atom, which can influence the compound's chemical properties and interactions. Ethyl 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylate is often studied for its potential applications in medicinal chemistry and as a building block in organic synthesis. Its properties may include solubility in organic solvents, moderate stability under standard conditions, and the ability to participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions. Overall, this compound represents an interesting subject for research due to its structural features and potential utility in various chemical applications.

CAS 3354-38-9

ethyl 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylate

5-Amino-3-thioxo-3H-(1,2)dithiole-4-carboxylic acid ethyl ester

Ref: 10-F009671