The chemical substance known as (5E)-5-(5-bromo-2-hydroxy-3-methoxybenzylidene)-3-ethyl-2-thioxo-1,3-thiazolidin-4-one, with the CAS number 359899-47-1, is a thiazolidinone derivative characterized by its unique structural features. This compound contains a thiazolidinone core, which is a five-membered ring containing sulfur and nitrogen, contributing to its potential biological activity. The presence of a bromine atom and a methoxy group on the aromatic ring enhances its reactivity and solubility properties. Additionally, the hydroxyl group may impart hydrogen-bonding capabilities, influencing its interaction with biological targets. The ethyl group attached to the thiazolidinone structure can affect the compound's lipophilicity and overall pharmacokinetic profile. Such compounds are often investigated for their potential therapeutic applications, including antimicrobial and anticancer activities, due to their ability to interact with various biological pathways. Overall, this substance exemplifies the complexity and diversity of thiazolidinone derivatives in medicinal chemistry.

(5E)-5-(5-bromo-2-hydroxy-3-methoxybenzylidene)-3-ethyl-2-thioxo-1,3-thiazolidin-4-one

359899-47-1: The chemical substance known as (5E)-5-(5-bromo-2-hydroxy-3-methoxybenzylidene)-3-ethyl-2-thioxo-1,3-thiazolidin-4-one, with the CAS number 359899-47-1, is a thiazolidinone derivative characterized by its unique structural features. This compound contains a thiazolidinone core, which is a five-membered ring containing sulfur and nitrogen, contributing to its potential biological activity. The presence of a bromine atom and a methoxy group on the aromatic ring enhances its reactivity and solubility properties. Additionally, the hydroxyl group may impart hydrogen-bonding capabilities, influencing its interaction with biological targets. The ethyl group attached to the thiazolidinone structure can affect the compound's lipophilicity and overall pharmacokinetic profile. Such compounds are often investigated for their potential therapeutic applications, including antimicrobial and anticancer activities, due to their ability to interact with various biological pathways. Overall, this substance exemplifies the complexity and diversity of thiazolidinone derivatives in medicinal chemistry.

CAS 359899-47-1

(5E)-5-(5-bromo-2-hydroxy-3-methoxybenzylidene)-3-ethyl-2-thioxo-1,3-thiazolidin-4-one

(5E)-5-(5-bromo-2-hydroxy-3-methoxybenzylidene)-3-ethyl-2-thioxo-1,3-thiazolidin-4-one

Ref: IN-DA00C60S

(5E)-5-(5-bromo-2-hydroxy-3-methoxybenzylidene)-3-ethyl-2-thioxo-1,3-thiazolidin-4-one

Ref: 10-F314483