4-Chloro-7-(2-furylmethyl)-5,6-dimethyl-7H-pyrrolo[2,3-d]pyrimidine is a heterocyclic organic compound characterized by its complex structure, which includes a pyrrolopyrimidine core. This compound features a chloro substituent at the 4-position and a furylmethyl group at the 7-position, along with two methyl groups at the 5 and 6 positions. The presence of the furan ring contributes to its potential reactivity and biological activity. Typically, such compounds may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The molecular structure suggests potential interactions with biological targets, which could be explored for therapeutic applications. Additionally, the compound's solubility, stability, and reactivity would depend on the specific functional groups and their arrangement, influencing its behavior in various chemical environments. As with many heterocycles, the compound may also participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, which could be relevant for synthetic applications.

4-CHLORO-7-(2-FURYLMETHYL)-5,6-DIMETHYL-7H-PYRROLO[2,3-D]PYRIMIDINE

103026-14-8: 4-Chloro-7-(2-furylmethyl)-5,6-dimethyl-7H-pyrrolo[2,3-d]pyrimidine is a heterocyclic organic compound characterized by its complex structure, which includes a pyrrolopyrimidine core. This compound features a chloro substituent at the 4-position and a furylmethyl group at the 7-position, along with two methyl groups at the 5 and 6 positions. The presence of the furan ring contributes to its potential reactivity and biological activity. Typically, such compounds may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The molecular structure suggests potential interactions with biological targets, which could be explored for therapeutic applications. Additionally, the compound's solubility, stability, and reactivity would depend on the specific functional groups and their arrangement, influencing its behavior in various chemical environments. As with many heterocycles, the compound may also participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, which could be relevant for synthetic applications.

CAS 103026-14-8

4-CHLORO-7-(2-FURYLMETHYL)-5,6-DIMETHYL-7H-PYRROLO[2,3-D]PYRIMIDINE

4-Chloro-7-(2-furylmethyl)-5,6-dimethyl-7h-pyrrolo[2,3-d]pyrimidine

Ref: IN-DA007YB4

4-Chloro-7-(furan-2-ylmethyl)-5,6-dimethyl-7H-pyrrolo[2,3-d]pyrimidine

Ref: 3D-DEA02614