4,5-Dichlorothieno[2,3-d]pyrimidine is a heterocyclic compound characterized by a fused ring system that incorporates both a thieno and a pyrimidine moiety. This compound features two chlorine substituents at the 4 and 5 positions of the thieno ring, which can significantly influence its chemical reactivity and biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of chlorine atoms enhances its electrophilic character, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Additionally, compounds of this type are often studied for their pharmacological properties, as they may exhibit antimicrobial, antiviral, or anticancer activities. The unique structural features of 4,5-dichlorothieno[2,3-d]pyrimidine contribute to its potential applications in medicinal chemistry and materials science. As with many heterocycles, the specific interactions and stability can be influenced by the surrounding functional groups and the overall molecular environment.

4,5-dichlorothieno[2,3-d]pyrimidine

137240-10-9: 4,5-Dichlorothieno[2,3-d]pyrimidine is a heterocyclic compound characterized by a fused ring system that incorporates both a thieno and a pyrimidine moiety. This compound features two chlorine substituents at the 4 and 5 positions of the thieno ring, which can significantly influence its chemical reactivity and biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of chlorine atoms enhances its electrophilic character, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Additionally, compounds of this type are often studied for their pharmacological properties, as they may exhibit antimicrobial, antiviral, or anticancer activities. The unique structural features of 4,5-dichlorothieno[2,3-d]pyrimidine contribute to its potential applications in medicinal chemistry and materials science. As with many heterocycles, the specific interactions and stability can be influenced by the surrounding functional groups and the overall molecular environment.

CAS 137240-10-9

4,5-dichlorothieno[2,3-d]pyrimidine

Thieno[2,3-d]pyrimidine, 4,5-dichloro-

Ref: IN-DA0012ZR

4,5-Dichlorothieno[2,3-d]pyrimidine

Ref: 54-OR1041897

4,5-Dichlorothieno[2,3-d]pyrimidine

Ref: 10-F219994