2-Chloro-7-iodo-5-methyl-5H-pyrrolo[3,2-d]pyrimidine is a heterocyclic organic compound characterized by its complex bicyclic structure, which incorporates both pyrrole and pyrimidine rings. This compound features a chlorine atom at the 2-position and an iodine atom at the 7-position, contributing to its reactivity and potential applications in medicinal chemistry. The presence of a methyl group at the 5-position enhances its lipophilicity, which can influence its biological activity and solubility. The unique arrangement of halogen substituents may also affect its electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. As a member of the pyrrolo-pyrimidine family, it may exhibit interesting pharmacological properties, potentially serving as a scaffold for drug development. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its stability and reactivity would be influenced by the electronic effects of the halogen substituents. Overall, this compound represents a valuable structure in the field of organic synthesis and medicinal chemistry.

2-chloro-7-iodo-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

1152475-62-1: 2-Chloro-7-iodo-5-methyl-5H-pyrrolo[3,2-d]pyrimidine is a heterocyclic organic compound characterized by its complex bicyclic structure, which incorporates both pyrrole and pyrimidine rings. This compound features a chlorine atom at the 2-position and an iodine atom at the 7-position, contributing to its reactivity and potential applications in medicinal chemistry. The presence of a methyl group at the 5-position enhances its lipophilicity, which can influence its biological activity and solubility. The unique arrangement of halogen substituents may also affect its electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. As a member of the pyrrolo-pyrimidine family, it may exhibit interesting pharmacological properties, potentially serving as a scaffold for drug development. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its stability and reactivity would be influenced by the electronic effects of the halogen substituents. Overall, this compound represents a valuable structure in the field of organic synthesis and medicinal chemistry.

5H-Pyrrolo[3,2-d]pyrimidine, 2-chloro-7-iodo-5-methyl-

2-Chloro-7-iodo-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

CAS 1152475-62-1

2-chloro-7-iodo-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

5H-Pyrrolo[3,2-d]pyrimidine, 2-chloro-7-iodo-5-methyl-

Ref: IN-DA000GI4

2-Chloro-7-iodo-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

Ref: 54-OR946102

2-Chloro-7-iodo-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

Ref: 10-F320256