6-Chloro-7-iodo-7-deazapurine

97%

  • Product Code: 97245
  Alias:    4-Chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine
  CAS:    123148-78-7
Molecular Weight: 279.47 g./mol Molecular Formula: C₆H₃ClIN₃
EC Number: MDL Number: MFCD09263258
Melting Point: 179-183 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: 6-Chloro-7-iodo-7-deazapurine is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various nucleoside analogs, which are crucial for the development of antiviral and anticancer agents. The compound's unique structure allows for modifications that can enhance the biological activity and selectivity of these therapeutic agents. Additionally, it is employed in biochemical research to study enzyme mechanisms and interactions, particularly those involving purine metabolism. Its halogenated structure makes it a valuable tool for probing the active sites of enzymes and understanding their catalytic processes.
Product Specification:
Test Specification
Melting point 179-183
PURITYHPLC 96.5-100
APPEARANCE OFF-WHITE TO BEIGE TO BROWN POWDER OR CRYSTAL
INFRARED SPECTRUM Conforms to Structure
NMR SPECTRUM 1H Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿300.00
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5.000 10-20 days ฿770.00
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25.000 10-20 days ฿3,820.00
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6-Chloro-7-iodo-7-deazapurine
6-Chloro-7-iodo-7-deazapurine is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various nucleoside analogs, which are crucial for the development of antiviral and anticancer agents. The compound's unique structure allows for modifications that can enhance the biological activity and selectivity of these therapeutic agents. Additionally, it is employed in biochemical research to study enzyme mechanisms and interactions, particularly those involving purine metabolism. Its halogenated structure makes it a valuable tool for probing the active sites of enzymes and understanding their catalytic processes.
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