Ethyl 2-(2,4-dichlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate, with the CAS number 262856-01-9, is a chemical compound characterized by its thiazole ring structure, which is a five-membered heterocyclic compound containing sulfur and nitrogen. This substance features a carboxylate ester functional group, contributing to its reactivity and solubility properties. The presence of the 2,4-dichlorophenyl group indicates that it has significant aromatic characteristics, which can influence its biological activity and interactions. The hydroxyl group on the thiazole ring enhances its potential for hydrogen bonding, affecting its solubility in polar solvents. This compound may exhibit various biological activities, making it of interest in pharmaceutical research. Its specific properties, such as melting point, boiling point, and solubility, would depend on the molecular interactions and the environment in which it is studied. Overall, this compound's unique structure suggests potential applications in medicinal chemistry and agrochemicals.

ethyl 2-(2,4-dichlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate

262856-01-9: Ethyl 2-(2,4-dichlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate, with the CAS number 262856-01-9, is a chemical compound characterized by its thiazole ring structure, which is a five-membered heterocyclic compound containing sulfur and nitrogen. This substance features a carboxylate ester functional group, contributing to its reactivity and solubility properties. The presence of the 2,4-dichlorophenyl group indicates that it has significant aromatic characteristics, which can influence its biological activity and interactions. The hydroxyl group on the thiazole ring enhances its potential for hydrogen bonding, affecting its solubility in polar solvents. This compound may exhibit various biological activities, making it of interest in pharmaceutical research. Its specific properties, such as melting point, boiling point, and solubility, would depend on the molecular interactions and the environment in which it is studied. Overall, this compound's unique structure suggests potential applications in medicinal chemistry and agrochemicals.

CAS 262856-01-9

ethyl 2-(2,4-dichlorophenyl)-4-hydroxy-1,3-thiazole-5-carboxylate

5-Thiazolecarboxylic acid, 2-(2,4-dichlorophenyl)-4-hydroxy-, ethyl ester

Ref: IN-DA002SL6

Ethyl 2-(2,4-dichlorophenyl)-4-hydroxythiazole-5-carboxylate

Ref: 54-OR2426

2-(2,4-Dichloro-phenyl)-4-hydroxy-thiazole-5-carboxylic acidethylester

Ref: 10-F478492