2-cyclopropyl-5-iodo-4-methyl-1H-imidazole

97%(HPLC) 

  • Product Code: 42160
  CAS:    1533442-94-2
Molecular Weight: 248.06 g./mol Molecular Formula: C₇H₉IN₂
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8℃
Product Description: This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a cyclopropyl group and an iodine atom, makes it a valuable intermediate in the creation of molecules with potential biological activity. Researchers often employ it in the design of enzyme inhibitors or receptor modulators, especially in the context of targeting specific pathways involved in diseases such as cancer or infections. Additionally, its imidazole core is advantageous in medicinal chemistry due to its ability to interact with biological targets through hydrogen bonding and π-π stacking interactions. The iodine atom also provides a convenient handle for further chemical modifications, such as cross-coupling reactions, to diversify the compound’s applications in drug discovery.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿9,000.00
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2-cyclopropyl-5-iodo-4-methyl-1H-imidazole
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a cyclopropyl group and an iodine atom, makes it a valuable intermediate in the creation of molecules with potential biological activity. Researchers often employ it in the design of enzyme inhibitors or receptor modulators, especially in the context of targeting specific pathways involved in diseases such as cancer or infections. Additionally, its imidazole core is advantageous in medicinal chemistry due to its ability to interact with biological targets through hydrogen bonding and π-π stacking interactions. The iodine atom also provides a convenient handle for further chemical modifications, such as cross-coupling reactions, to diversify the compound’s applications in drug discovery.
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