1-Methyl-5-nitroimidazole

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Reagent Code: #206207
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CAS Number 3034-42-2

science Other reagents with same CAS 3034-42-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 127.10 g/mol
Formula C₄H₅N₃O₂
badge Registry Numbers
MDL Number MFCD00126968
thermostat Physical Properties
Melting Point 54-57°C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the production of antiprotozoal and antibacterial agents. It serves as a building block for more complex imidazole derivatives, such as metronidazole and tinidazole, which are widely used to treat infections caused by anaerobic bacteria and protozoa. Its nitro group and methyl substitution make it suitable for further chemical modifications in drug development. Also employed in research settings for designing new bioactive molecules and studying structure-activity relationships in nitroimidazole-based drugs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿180.00
5g
10-20 days ฿500.00
25g
10-20 days ฿1,780.00
1-Methyl-5-nitroimidazole
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the production of antiprotozoal and antibacterial agents. It serves as a building block for more complex imidazole derivatives, such as metronidazole and tinidazole, which are widely used to treat infections caused by anaerobic bacteria and protozoa. Its nitro group and methyl substitution make it suitable for further chemical modifications in drug development. Also employed in research settings for designing

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the production of antiprotozoal and antibacterial agents. It serves as a building block for more complex imidazole derivatives, such as metronidazole and tinidazole, which are widely used to treat infections caused by anaerobic bacteria and protozoa. Its nitro group and methyl substitution make it suitable for further chemical modifications in drug development. Also employed in research settings for designing new bioactive molecules and studying structure-activity relationships in nitroimidazole-based drugs.

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