2,6,8-Trichloro-7-methylpurine is a synthetic purine derivative characterized by the presence of three chlorine atoms and a methyl group attached to its purine structure. This compound is typically recognized for its role in biochemical research, particularly in studies related to nucleic acids and their analogs. The chlorination at positions 2, 6, and 8 of the purine ring significantly alters its chemical reactivity and biological activity compared to unmodified purines. It is often utilized in the synthesis of nucleoside analogs and can exhibit properties such as antimicrobial or antiviral activity, depending on its specific interactions within biological systems. The presence of the methyl group at position 7 can influence the compound's solubility and stability. As with many halogenated compounds, 2,6,8-trichloro-7-methylpurine may also pose environmental and health risks, necessitating careful handling and disposal in laboratory settings. Overall, its unique structure makes it a valuable compound in medicinal chemistry and molecular biology research.

2,6,8-trichloro-7-methylpurine

16404-16-3: 2,6,8-trichloro-7-methyl-7H-purine

CAS 16404-16-3: 2,6,8-trichloro-7-methylpurine

2,6,8-Trichloro-7-methyl-7H-purine

Ref: 3D-RAA40416

2,6,8-Trichloro-7-Methyl Purine

Ref: 4Z-P-185004

7H-Purine, 2,6,8-trichloro-7-methyl-

Ref: IN-DA001ULV