5-Iodo-4-methyl-1H-imidazole

≥95%

Reagent Code: #200251
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CAS Number 15813-07-7

science Other reagents with same CAS 15813-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.00 g/mol
Formula C₄H₅IN₂
badge Registry Numbers
MDL Number MFCD07783894
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building more complex molecules. Commonly employed in research settings to create imidazole-based compounds that exhibit biological activity. Also utilized in the preparation of kinase inhibitors and other targeted therapies. Its iodine moiety facilitates coupling reactions, especially in palladium-catalyzed cross-coupling processes, enabling the formation of carbon-carbon bonds in drug discovery pipelines.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,570.00
inventory 10g
10-20 days ฿3,080.00
inventory 25g
10-20 days ฿7,440.00
inventory 100g
10-20 days ฿25,160.00
5-Iodo-4-methyl-1H-imidazole
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building more complex molecules. Commonly employed in research settings to create imidazole-based compounds that exhibit biological activity. Also utilized in the preparation of kinase inhibitors and other targeted therapies. Its iodine moiety facilitates coupling reactions, espec

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building more complex molecules. Commonly employed in research settings to create imidazole-based compounds that exhibit biological activity. Also utilized in the preparation of kinase inhibitors and other targeted therapies. Its iodine moiety facilitates coupling reactions, especially in palladium-catalyzed cross-coupling processes, enabling the formation of carbon-carbon bonds in drug discovery pipelines.

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