2-(4-Chlorophenyl)-1,3-thiazolidine is a heterocyclic organic compound characterized by a thiazolidine ring, which contains both sulfur and nitrogen atoms. The presence of the 4-chlorophenyl group indicates that there is a chlorinated phenyl substituent attached to the thiazolidine structure, influencing its chemical reactivity and physical properties. This compound typically exhibits a range of biological activities, making it of interest in medicinal chemistry. It may possess properties such as antimicrobial or anti-inflammatory effects, depending on its specific structure and substituents. The thiazolidine ring contributes to its potential as a ligand in coordination chemistry and as a scaffold in drug design. In terms of physical properties, compounds like this often have moderate solubility in organic solvents and may exhibit distinct melting and boiling points. Safety and handling considerations are essential, as with many organic compounds, particularly those containing halogens. Overall, 2-(4-chlorophenyl)-1,3-thiazolidine is a compound of interest in various fields, including pharmaceuticals and materials science.

2-(4-chlorophenyl)-1,3-thiazolidine

7738-99-0: 2-(4-Chlorophenyl)-1,3-thiazolidine is a heterocyclic organic compound characterized by a thiazolidine ring, which contains both sulfur and nitrogen atoms. The presence of the 4-chlorophenyl group indicates that there is a chlorinated phenyl substituent attached to the thiazolidine structure, influencing its chemical reactivity and physical properties. This compound typically exhibits a range of biological activities, making it of interest in medicinal chemistry. It may possess properties such as antimicrobial or anti-inflammatory effects, depending on its specific structure and substituents. The thiazolidine ring contributes to its potential as a ligand in coordination chemistry and as a scaffold in drug design. In terms of physical properties, compounds like this often have moderate solubility in organic solvents and may exhibit distinct melting and boiling points. Safety and handling considerations are essential, as with many organic compounds, particularly those containing halogens. Overall, 2-(4-chlorophenyl)-1,3-thiazolidine is a compound of interest in various fields, including pharmaceuticals and materials science.

CAS 7738-99-0

2-(4-chlorophenyl)-1,3-thiazolidine

2-(4-Chlorophenyl)thiazolidine

Ref: IN-DA008MZ2

2-(4-Chlorophenyl)thiazolidine

Ref: 54-OR1055822

2-(4-Chloro-phenyl)-thiazolidine

Ref: 10-F025628