5-Nitro-1H-imidazole-4-carbaldehyde

97%

Reagent Code: #217356
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CAS Number 81246-34-6

science Other reagents with same CAS 81246-34-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 141.09 g/mol
Formula C₄H₃N₃O₃
thermostat Physical Properties
Melting Point 213-215°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of nitroimidazole-based pharmaceuticals, particularly in the development of antiprotozoal and antibacterial agents. Its aldehyde functional group allows for easy modification and coupling reactions, making it valuable in medicinal chemistry for building more complex molecules. Commonly employed in the preparation of derivatives targeting anaerobic pathogens, it plays a role in research focused on improving drug efficacy and reducing resistance in treatments for infections such as trichomoniasis, giardiasis, and certain bacterial diseases. Also utilized in the development of labeled compounds for biochemical assays and imaging studies due to its reactive site for conjugation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,270.00
inventory 100mg
10-20 days ฿4,980.00
inventory 250mg
10-20 days ฿9,580.00
5-Nitro-1H-imidazole-4-carbaldehyde
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Used as a key intermediate in the synthesis of nitroimidazole-based pharmaceuticals, particularly in the development of antiprotozoal and antibacterial agents. Its aldehyde functional group allows for easy modification and coupling reactions, making it valuable in medicinal chemistry for building more complex molecules. Commonly employed in the preparation of derivatives targeting anaerobic pathogens, it plays a role in research focused on improving drug efficacy and reducing resistance in treatments for infections such as trichomoniasis, giardiasis, and certain bacterial diseases. Also utilized in the development of labeled compounds for biochemical assays and imaging studies due to its reactive site for conjugation.
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