5-((4-(Dimethylamino)phenyl)methylene)-3-ethyl-2-thioxo-1,3-thiazolidin-4-one is a thiazolidinone derivative characterized by its unique thiazolidine ring structure, which incorporates both sulfur and nitrogen atoms. This compound features a thioxo group, contributing to its potential reactivity and biological activity. The presence of a dimethylamino group enhances its solubility and may influence its pharmacological properties, making it of interest in medicinal chemistry. The ethyl group attached to the thiazolidine ring can affect the compound's steric and electronic properties, potentially impacting its interactions with biological targets. This substance may exhibit various biological activities, including antimicrobial or anticancer properties, due to its structural features. Its CAS number, 1351484-76-8, allows for easy identification in chemical databases. As with many thiazolidinones, the compound's characteristics, including its stability, solubility, and reactivity, can be influenced by environmental conditions such as pH and temperature, making it a subject of interest for further research in synthetic and medicinal chemistry.

5-((4-(DIMETHYLAMINO)PHENYL)METHYLENE)-3-ETHYL-2-THIOXO-1,3-THIAZOLIDIN-4-ONE

1351484-76-8: 5-((4-(Dimethylamino)phenyl)methylene)-3-ethyl-2-thioxo-1,3-thiazolidin-4-one is a thiazolidinone derivative characterized by its unique thiazolidine ring structure, which incorporates both sulfur and nitrogen atoms. This compound features a thioxo group, contributing to its potential reactivity and biological activity. The presence of a dimethylamino group enhances its solubility and may influence its pharmacological properties, making it of interest in medicinal chemistry. The ethyl group attached to the thiazolidine ring can affect the compound's steric and electronic properties, potentially impacting its interactions with biological targets. This substance may exhibit various biological activities, including antimicrobial or anticancer properties, due to its structural features. Its CAS number, 1351484-76-8, allows for easy identification in chemical databases. As with many thiazolidinones, the compound's characteristics, including its stability, solubility, and reactivity, can be influenced by environmental conditions such as pH and temperature, making it a subject of interest for further research in synthetic and medicinal chemistry.

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CAS 1351484-76-8

5-((4-(DIMETHYLAMINO)PHENYL)METHYLENE)-3-ETHYL-2-THIOXO-1,3-THIAZOLIDIN-4-ONE

5-((4-(dimethylamino)phenyl)methylene)-3-ethyl-2-thioxo-1,3-thiazolidin-4-one

Ref: 3D-BEC48476