4-Chloro-7-cyclopentyl-5-iodo-7H-pyrrolo[2,3-d]pyrimidine is a heterocyclic compound characterized by a fused pyrrole and pyrimidine structure, which contributes to its unique chemical properties. The presence of chlorine and iodine substituents enhances its reactivity and potential biological activity. The cyclopentyl group introduces a hydrophobic character, which can influence its solubility and interaction with biological targets. This compound may exhibit interesting pharmacological properties, making it a candidate for research in medicinal chemistry, particularly in the development of novel therapeutics. Its molecular structure suggests potential for interactions with various biological macromolecules, including enzymes and receptors. Additionally, the halogen atoms can participate in halogen bonding, which may further modulate its biological activity. As with many heterocycles, the stability and reactivity of this compound can be influenced by environmental factors such as pH and temperature, making it important to consider these conditions in experimental applications. Overall, 4-chloro-7-cyclopentyl-5-iodo-7H-pyrrolo[2,3-d]pyrimidine represents a complex and potentially valuable chemical entity in the field of drug discovery.

4-CHLORO-7-CYCLOPENTYL-5-IODO-7H-PYRROLO[2,3-D]PYRIMIDINE

213745-17-6: 4-Chloro-7-cyclopentyl-5-iodo-7H-pyrrolo[2,3-d]pyrimidine is a heterocyclic compound characterized by a fused pyrrole and pyrimidine structure, which contributes to its unique chemical properties. The presence of chlorine and iodine substituents enhances its reactivity and potential biological activity. The cyclopentyl group introduces a hydrophobic character, which can influence its solubility and interaction with biological targets. This compound may exhibit interesting pharmacological properties, making it a candidate for research in medicinal chemistry, particularly in the development of novel therapeutics. Its molecular structure suggests potential for interactions with various biological macromolecules, including enzymes and receptors. Additionally, the halogen atoms can participate in halogen bonding, which may further modulate its biological activity. As with many heterocycles, the stability and reactivity of this compound can be influenced by environmental factors such as pH and temperature, making it important to consider these conditions in experimental applications. Overall, 4-chloro-7-cyclopentyl-5-iodo-7H-pyrrolo[2,3-d]pyrimidine represents a complex and potentially valuable chemical entity in the field of drug discovery.

CAS 213745-17-6

4-CHLORO-7-CYCLOPENTYL-5-IODO-7H-PYRROLO[2,3-D]PYRIMIDINE

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

Ref: IN-DA007QP6

4-CHLORO-7-CYCLOPENTYL-5-IODO-7H-PYRROLO[2,3-D]PYRIMIDINE

Ref: 10-F334097