Ethyl 2-(2,3-dichlorophenyl)-1,3-thiazole-4-carboxylate is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features a carboxylate ester functional group, contributing to its reactivity and solubility properties. The presence of the 2,3-dichlorophenyl substituent indicates that it has two chlorine atoms attached to a phenyl ring, which can influence its biological activity and lipophilicity. Ethyl 2-(2,3-dichlorophenyl)-1,3-thiazole-4-carboxylate is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The compound's specific properties, such as melting point, boiling point, and solubility, would depend on its molecular interactions and the presence of functional groups. As with many thiazole derivatives, it may also exhibit interesting biological activities, making it a subject of interest in medicinal chemistry.

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

175276-86-5: Ethyl 2-(2,3-dichlorophenyl)-1,3-thiazole-4-carboxylate is a chemical compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features a carboxylate ester functional group, contributing to its reactivity and solubility properties. The presence of the 2,3-dichlorophenyl substituent indicates that it has two chlorine atoms attached to a phenyl ring, which can influence its biological activity and lipophilicity. Ethyl 2-(2,3-dichlorophenyl)-1,3-thiazole-4-carboxylate is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The compound's specific properties, such as melting point, boiling point, and solubility, would depend on its molecular interactions and the presence of functional groups. As with many thiazole derivatives, it may also exhibit interesting biological activities, making it a subject of interest in medicinal chemistry.

CAS 175276-86-5

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

Ethyl 2-(2,3-dichlorophenyl)thiazole-4-carboxylate

Ref: IN-DA0020RU

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

Ref: 54-OR29645

Ethyl 2-(2,3-dichlorophenyl)thiazole-4-carboxylate

Ref: 10-F437482