CAS 203436-45-7
:9H-Purine, 2,6-dichloro-9-(1-methylethyl)-
Description:
9H-Purine, 2,6-dichloro-9-(1-methylethyl)-, identified by its CAS number 203436-45-7, is a chemical compound belonging to the purine class, which is characterized by a fused double-ring structure containing nitrogen atoms. This specific compound features two chlorine substituents at the 2 and 6 positions of the purine ring, along with an isopropyl group at the 9 position. The presence of these substituents can significantly influence its chemical reactivity, solubility, and biological activity. Purines are essential components of nucleic acids and play critical roles in cellular processes, including energy transfer and signal transduction. The dichloro and isopropyl groups may impart unique properties that could be relevant in pharmaceutical applications or as research tools. As with many purine derivatives, this compound may exhibit interactions with biological systems, making it of interest in medicinal chemistry and biochemistry. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or environmental impact.
Formula:C8H8Cl2N4
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Found 4 products.
9H-Purine, 2,6-dichloro-9-(1-methylethyl)-
CAS:Formula:C8H8Cl2N4Purity:96%Color and Shape:SolidMolecular weight:231.08192,6-Dichloro-9-isopropyl-9H-purine
CAS:<p>2,6-Dichloro-9-isopropyl-9H-purine</p>Purity:≥95%Molecular weight:231.08g/mol2,6-Dichloro-9-isopropyl-9H-purine
CAS:Formula:C8H8Cl2N4Purity:96%Color and Shape:SolidMolecular weight:231.082,6-Dichloro-9-isopropylpurine
CAS:Controlled Product<p>Applications Bohemine cyclin-dependent kinase inhibitor for the treatment of leukemia or other cancer.<br>References Malumbres, M., et al.: Biol. Chem., 381 827 (2000), Li, M., et al.: J. Biol. Chem., 277, 46385 (2002), Li, M., et al.: J. Biol. Chem., 279, 17459 (2004).<br></p>Formula:C8H8Cl2N4Color and Shape:NeatMolecular weight:231.08
