4-Iodo-1-trityl-1H-imidazole

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Reagent Code: #199290
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CAS Number 96797-15-8

science Other reagents with same CAS 96797-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 436.29 g/mol
Formula C₂₂H₁₇IN₂
badge Registry Numbers
MDL Number MFCD02179542
thermostat Physical Properties
Melting Point 224 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in antiviral and anticancer agents. Its primary role is in the protection of imidazole nitrogen during multi-step organic syntheses, allowing selective reactions at other molecular sites. The trityl group provides steric bulk and stability, while the iodo functionality enables further coupling reactions, such as palladium-catalyzed cross-couplings, to introduce aromatic or heteroaromatic moieties. Commonly applied in the development of nucleoside analogs and kinase inhibitors.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿810.00
inventory 25g
10-20 days ฿3,670.00
inventory 100g
10-20 days ฿12,370.00

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4-Iodo-1-trityl-1H-imidazole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in antiviral and anticancer agents. Its primary role is in the protection of imidazole nitrogen during multi-step organic syntheses, allowing selective reactions at other molecular sites. The trityl group provides steric bulk and stability, while the iodo functionality enables further coupling reactions, such as palladium-catalyzed cross-couplings, to introduce aromatic or heteroaromatic moieties. Commonly applied in th

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in antiviral and anticancer agents. Its primary role is in the protection of imidazole nitrogen during multi-step organic syntheses, allowing selective reactions at other molecular sites. The trityl group provides steric bulk and stability, while the iodo functionality enables further coupling reactions, such as palladium-catalyzed cross-couplings, to introduce aromatic or heteroaromatic moieties. Commonly applied in the development of nucleoside analogs and kinase inhibitors.

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