2-(4-Methylphenyl)-1,3-thiazolidine is a heterocyclic organic compound characterized by a thiazolidine ring, which contains both sulfur and nitrogen atoms in its five-membered structure. The presence of the 4-methylphenyl group indicates that there is a methyl substituent on a phenyl ring attached to the thiazolidine, contributing to its aromatic properties. This compound typically exhibits a range of chemical properties, including moderate solubility in organic solvents and potential reactivity due to the presence of the thiazolidine ring, which can participate in various chemical reactions such as nucleophilic substitutions or cyclizations. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as thiazolidine derivatives are often explored for their biological activities. Additionally, the compound may exhibit specific stereochemical configurations, influencing its reactivity and interactions with biological targets. Overall, 2-(4-methylphenyl)-1,3-thiazolidine is of interest for its unique structural features and potential utility in various chemical and pharmaceutical applications.

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

67086-82-2: 2-(4-Methylphenyl)-1,3-thiazolidine is a heterocyclic organic compound characterized by a thiazolidine ring, which contains both sulfur and nitrogen atoms in its five-membered structure. The presence of the 4-methylphenyl group indicates that there is a methyl substituent on a phenyl ring attached to the thiazolidine, contributing to its aromatic properties. This compound typically exhibits a range of chemical properties, including moderate solubility in organic solvents and potential reactivity due to the presence of the thiazolidine ring, which can participate in various chemical reactions such as nucleophilic substitutions or cyclizations. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as thiazolidine derivatives are often explored for their biological activities. Additionally, the compound may exhibit specific stereochemical configurations, influencing its reactivity and interactions with biological targets. Overall, 2-(4-methylphenyl)-1,3-thiazolidine is of interest for its unique structural features and potential utility in various chemical and pharmaceutical applications.

CAS 67086-82-2

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

2-(p-Tolyl)thiazolidine

Ref: 54-OR1068717

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

Ref: 10-F520601