The chemical substance known as (5Z)-5-(3-bromo-4-hydroxy-5-methoxybenzylidene)-3-methyl-2-thioxo-1,3-thiazolidin-4-one, with the CAS number 58215-51-3, is a thiazolidinone derivative characterized by its thiazolidine ring structure, which incorporates a thione functional group. This compound features a substituted benzylidene moiety, where the benzene ring is further modified with bromine, hydroxy, and methoxy groups, contributing to its potential biological activity. The presence of the thioxo group suggests that it may exhibit properties typical of thioketones, such as reactivity in nucleophilic addition reactions. The specific stereochemistry indicated by the (5Z) configuration suggests a particular geometric arrangement that may influence its interaction with biological targets. Compounds of this class are often investigated for their pharmacological properties, including antimicrobial and anti-inflammatory activities. Overall, the unique combination of functional groups and structural features makes this compound of interest in medicinal chemistry and drug development.

(5Z)-5-(3-bromo-4-hydroxy-5-methoxybenzylidene)-3-methyl-2-thioxo-1,3-thiazolidin-4-one

58215-51-3: The chemical substance known as (5Z)-5-(3-bromo-4-hydroxy-5-methoxybenzylidene)-3-methyl-2-thioxo-1,3-thiazolidin-4-one, with the CAS number 58215-51-3, is a thiazolidinone derivative characterized by its thiazolidine ring structure, which incorporates a thione functional group. This compound features a substituted benzylidene moiety, where the benzene ring is further modified with bromine, hydroxy, and methoxy groups, contributing to its potential biological activity. The presence of the thioxo group suggests that it may exhibit properties typical of thioketones, such as reactivity in nucleophilic addition reactions. The specific stereochemistry indicated by the (5Z) configuration suggests a particular geometric arrangement that may influence its interaction with biological targets. Compounds of this class are often investigated for their pharmacological properties, including antimicrobial and anti-inflammatory activities. Overall, the unique combination of functional groups and structural features makes this compound of interest in medicinal chemistry and drug development.

CAS 58215-51-3

(5Z)-5-(3-bromo-4-hydroxy-5-methoxybenzylidene)-3-methyl-2-thioxo-1,3-thiazolidin-4-one

(5Z)-5-(3-bromo-4-hydroxy-5-methoxybenzylidene)-3-methyl-2-thioxo-1,3-thiazolidin-4-one

Ref: 10-F314617