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

97%(HPLC) 

Reagent Code: #42160
fingerprint
CAS Number 1533442-94-2

science Other reagents with same CAS 1533442-94-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.06 g/mol
Formula C₇H₉IN₂
inventory_2 Storage & Handling
Storage 2-8℃

description 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-cyclopropyl-5-iodo-4-methyl-1H-imidazole
No image available
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.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...