The chemical substance known as (5E)-5-(naphthalen-2-ylmethylidene)-2-thioxo-1,3-thiazolidin-4-one, with the CAS number 107916-92-7, is a thiazolidinone derivative characterized by a thiazolidine ring containing a thione functional group. This compound features a naphthylmethylidene substituent, which contributes to its potential biological activity and molecular interactions. Thiazolidinones are known for their diverse pharmacological properties, including anti-inflammatory, antimicrobial, and antidiabetic effects. The presence of the naphthalene moiety may enhance lipophilicity and facilitate interactions with biological targets. The compound's structure suggests it may participate in various chemical reactions, such as nucleophilic attacks or cyclization, due to the reactivity of the thione group. Additionally, its stability and solubility can be influenced by the substituents on the thiazolidine ring and the naphthalene group. Overall, this compound represents a class of molecules with significant interest in medicinal chemistry and potential therapeutic applications.

(5E)-5-(naphthalen-2-ylmethylidene)-2-thioxo-1,3-thiazolidin-4-one

107916-92-7: The chemical substance known as (5E)-5-(naphthalen-2-ylmethylidene)-2-thioxo-1,3-thiazolidin-4-one, with the CAS number 107916-92-7, is a thiazolidinone derivative characterized by a thiazolidine ring containing a thione functional group. This compound features a naphthylmethylidene substituent, which contributes to its potential biological activity and molecular interactions. Thiazolidinones are known for their diverse pharmacological properties, including anti-inflammatory, antimicrobial, and antidiabetic effects. The presence of the naphthalene moiety may enhance lipophilicity and facilitate interactions with biological targets. The compound's structure suggests it may participate in various chemical reactions, such as nucleophilic attacks or cyclization, due to the reactivity of the thione group. Additionally, its stability and solubility can be influenced by the substituents on the thiazolidine ring and the naphthalene group. Overall, this compound represents a class of molecules with significant interest in medicinal chemistry and potential therapeutic applications.

CAS 107916-92-7

(5E)-5-(naphthalen-2-ylmethylidene)-2-thioxo-1,3-thiazolidin-4-one

(5E)-2-Mercapto-5-(2-naphthylmethylene)-1,3-thiazol-4(5H)-one

Ref: IN-DA00847V

(5E)-2-mercapto-5-(2-naphthylmethylene)-1,3-thiazol-4(5H)-one

Ref: 10-F307868