2-(3,5-Dichlorophenyl)-1,3-thiazolidine is a chemical compound characterized by its thiazolidine ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. The presence of the 3,5-dichlorophenyl group indicates that the compound has two chlorine substituents on a phenyl ring, which can significantly influence its chemical reactivity and biological activity. This compound may exhibit properties typical of thiazolidines, such as potential antimicrobial or anti-inflammatory activities, due to the presence of the thiazolidine moiety. Its molecular structure suggests that it may participate in various chemical reactions, including nucleophilic substitutions and cyclization processes. The compound's solubility, stability, and reactivity can be affected by the electron-withdrawing nature of the chlorine atoms, which can also impact its interactions in biological systems. As with many thiazolidine derivatives, it may have applications in medicinal chemistry, particularly in the development of pharmaceuticals. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.

2-(3,5-dichlorophenyl)-1,3-thiazolidine

83522-15-0: 2-(3,5-Dichlorophenyl)-1,3-thiazolidine is a chemical compound characterized by its thiazolidine ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. The presence of the 3,5-dichlorophenyl group indicates that the compound has two chlorine substituents on a phenyl ring, which can significantly influence its chemical reactivity and biological activity. This compound may exhibit properties typical of thiazolidines, such as potential antimicrobial or anti-inflammatory activities, due to the presence of the thiazolidine moiety. Its molecular structure suggests that it may participate in various chemical reactions, including nucleophilic substitutions and cyclization processes. The compound's solubility, stability, and reactivity can be affected by the electron-withdrawing nature of the chlorine atoms, which can also impact its interactions in biological systems. As with many thiazolidine derivatives, it may have applications in medicinal chemistry, particularly in the development of pharmaceuticals. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.

CAS 83522-15-0

2-(3,5-dichlorophenyl)-1,3-thiazolidine