Ethyl 4-chlorothieno[3,2-d]pyrimidine-2-carboxylate is a heterocyclic compound characterized by its unique structure, which includes a thieno[3,2-d]pyrimidine core. This compound features a carboxylate ester functional group, specifically an ethyl ester, which contributes to its chemical reactivity and solubility properties. The presence of a chlorine atom at the 4-position of the pyrimidine ring enhances its electrophilic character, making it potentially useful in various chemical reactions, including nucleophilic substitutions. Ethyl 4-chlorothieno[3,2-d]pyrimidine-2-carboxylate may exhibit biological activity, which could be of interest in pharmaceutical research, particularly in the development of new therapeutic agents. Its molecular structure suggests potential applications in agrochemicals or as a building block in organic synthesis. The compound's stability, solubility, and reactivity can be influenced by the surrounding functional groups and the overall molecular geometry. As with many heterocycles, it may also display interesting electronic properties, making it a subject of study in materials science and organic electronics.

ethyl 4-chlorothieno[3,2-d]pyrimidine-2-carboxylate

319442-18-7: Ethyl 4-chlorothieno[3,2-d]pyrimidine-2-carboxylate is a heterocyclic compound characterized by its unique structure, which includes a thieno[3,2-d]pyrimidine core. This compound features a carboxylate ester functional group, specifically an ethyl ester, which contributes to its chemical reactivity and solubility properties. The presence of a chlorine atom at the 4-position of the pyrimidine ring enhances its electrophilic character, making it potentially useful in various chemical reactions, including nucleophilic substitutions. Ethyl 4-chlorothieno[3,2-d]pyrimidine-2-carboxylate may exhibit biological activity, which could be of interest in pharmaceutical research, particularly in the development of new therapeutic agents. Its molecular structure suggests potential applications in agrochemicals or as a building block in organic synthesis. The compound's stability, solubility, and reactivity can be influenced by the surrounding functional groups and the overall molecular geometry. As with many heterocycles, it may also display interesting electronic properties, making it a subject of study in materials science and organic electronics.

CAS 319442-18-7

ethyl 4-chlorothieno[3,2-d]pyrimidine-2-carboxylate

Ethyl 4-chlorothieno[3,2-d]pyrimidine-2-carboxylate

Ref: IN-DA007I4F

Ethyl 4-chlorothieno[3,2-d]pyrimidine-2-carboxylate

Ref: 10-F077478