4-Iodoimidazole

97%

Reagent Code: #199266
label
Alias 4-Iodine-1(H)-imidazole, 5-Iodine-1(H)-imidazole, 4(5)-Iodine-imidazole
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CAS Number 71759-89-2

science Other reagents with same CAS 71759-89-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.97 g/mol
Formula C₃H₃IN₂
badge Registry Numbers
MDL Number MFCD01632213
thermostat Physical Properties
Melting Point 137-138°C
inventory_2 Storage & Handling
Storage -20°C, avoiding light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with biological activity. Commonly employed in antifungal, antiparasitic, and anticancer agent preparations due to its ability to modify bioactive molecules. Also utilized in agrochemicals for creating fungicides and in materials science for constructing nitrogen-rich heterocyclic frameworks. Its iodine functionality allows for further derivatization via cross-coupling reactions, making it valuable in medicinal chemistry research and drug discovery processes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿138.00
1g
10-20 days ฿174.00
5g
10-20 days ฿670.00
25g
10-20 days ฿3,170.00
100g
10-20 days ฿10,780.00
4-Iodoimidazole
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with biological activity. Commonly employed in antifungal, antiparasitic, and anticancer agent preparations due to its ability to modify bioactive molecules. Also utilized in agrochemicals for creating fungicides and in materials science for constructing nitrogen-rich heterocyclic frameworks. Its iodine functionality allows for further derivatization via cross-coupling reactions, makin

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with biological activity. Commonly employed in antifungal, antiparasitic, and anticancer agent preparations due to its ability to modify bioactive molecules. Also utilized in agrochemicals for creating fungicides and in materials science for constructing nitrogen-rich heterocyclic frameworks. Its iodine functionality allows for further derivatization via cross-coupling reactions, making it valuable in medicinal chemistry research and drug discovery processes.

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