5-(5-Chlorothiophen-2-yl)-5-methylimidazolidine-2,4-dione, with the CAS number 62032-04-6, is a chemical compound that features a unique structure combining an imidazolidine ring with a chlorothiophene substituent. This compound typically exhibits characteristics such as moderate solubility in organic solvents, which may vary depending on the solvent's polarity. The presence of the chlorothiophene moiety can impart specific electronic properties, potentially influencing its reactivity and interaction with biological systems. The imidazolidine ring contributes to the compound's stability and may participate in various chemical reactions, including nucleophilic substitutions or cyclization processes. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its synthesis and characterization often involve standard organic chemistry techniques, including NMR spectroscopy and mass spectrometry, to confirm its structure and purity. Overall, 5-(5-chlorothiophen-2-yl)-5-methylimidazolidine-2,4-dione represents a versatile scaffold for further chemical exploration and potential applications in medicinal chemistry.

5-(5-chlorothiophen-2-yl)-5-methylimidazolidine-2,4-dione

62032-04-6: 5-(5-Chlorothiophen-2-yl)-5-methylimidazolidine-2,4-dione, with the CAS number 62032-04-6, is a chemical compound that features a unique structure combining an imidazolidine ring with a chlorothiophene substituent. This compound typically exhibits characteristics such as moderate solubility in organic solvents, which may vary depending on the solvent's polarity. The presence of the chlorothiophene moiety can impart specific electronic properties, potentially influencing its reactivity and interaction with biological systems. The imidazolidine ring contributes to the compound's stability and may participate in various chemical reactions, including nucleophilic substitutions or cyclization processes. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its synthesis and characterization often involve standard organic chemistry techniques, including NMR spectroscopy and mass spectrometry, to confirm its structure and purity. Overall, 5-(5-chlorothiophen-2-yl)-5-methylimidazolidine-2,4-dione represents a versatile scaffold for further chemical exploration and potential applications in medicinal chemistry.

CAS 62032-04-6

5-(5-chlorothiophen-2-yl)-5-methylimidazolidine-2,4-dione

5-(5-Chlorothiophen-2-yl)-5-methylimidazolidine-2,4-dione

Ref: 3D-MCA03204