The chemical substance known as (5Z)-5-[(2-methoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione, with the CAS number 1307299-54-2, is a thiazolidinedione derivative characterized by its unique structural features. This compound contains a thiazolidine ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen atoms. The presence of a methoxyphenyl group contributes to its potential biological activity, as substituents on aromatic rings can influence the compound's interaction with biological targets. The (5Z) configuration indicates a specific geometric arrangement around the double bond, which can affect the compound's reactivity and stability. Thiazolidinediones are known for their role in medicinal chemistry, particularly in the development of antidiabetic agents, due to their ability to enhance insulin sensitivity. The compound's properties, such as solubility, melting point, and reactivity, would be influenced by its molecular structure and functional groups. Overall, this substance represents a class of compounds with significant interest in pharmacological research and potential therapeutic applications.

(5Z)-5-[(2-methoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione

1307299-54-2: The chemical substance known as (5Z)-5-[(2-methoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione, with the CAS number 1307299-54-2, is a thiazolidinedione derivative characterized by its unique structural features. This compound contains a thiazolidine ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen atoms. The presence of a methoxyphenyl group contributes to its potential biological activity, as substituents on aromatic rings can influence the compound's interaction with biological targets. The (5Z) configuration indicates a specific geometric arrangement around the double bond, which can affect the compound's reactivity and stability. Thiazolidinediones are known for their role in medicinal chemistry, particularly in the development of antidiabetic agents, due to their ability to enhance insulin sensitivity. The compound's properties, such as solubility, melting point, and reactivity, would be influenced by its molecular structure and functional groups. Overall, this substance represents a class of compounds with significant interest in pharmacological research and potential therapeutic applications.

5-[(2-methoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione

(Z)-5-(2-Methoxybenzylidene)thiazolidine-2,4-dione

CAS 1307299-54-2

(5Z)-5-[(2-methoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione

5-[(2-methoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione

Ref: IN-DA01C1QM

(Z)-5-(2-Methoxybenzylidene)thiazolidine-2,4-dione

Ref: 54-OR1049229