2-(2-Nitro-1H-imidazol-1-yl)acetic acid

≥95%

Reagent Code: #218082
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CAS Number 22813-32-7

science Other reagents with same CAS 22813-32-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.11 g/mol
Formula C₅H₅N₃O₄
badge Registry Numbers
MDL Number MFCD12022607
thermostat Physical Properties
Boiling Point 487.2°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.71g/cm3
Storage 2-8°C, dry seal

description Product Description

Used as an intermediate in the synthesis of nitroimidazole-based pharmaceuticals, particularly in the development of antimicrobial and antiparasitic agents. Its structure supports the formation of bioreductive compounds that are active under hypoxic conditions, making it valuable in designing drugs for targeting anaerobic pathogens and certain tumor cells. Also employed in research for prodrug development, where selective activation in low-oxygen environments enhances therapeutic specificity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,830.00
inventory 250mg
10-20 days ฿4,760.00
inventory 1g
10-20 days ฿13,320.00
inventory 5g
10-20 days ฿56,780.00

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2-(2-Nitro-1H-imidazol-1-yl)acetic acid
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Used as an intermediate in the synthesis of nitroimidazole-based pharmaceuticals, particularly in the development of antimicrobial and antiparasitic agents. Its structure supports the formation of bioreductive compounds that are active under hypoxic conditions, making it valuable in designing drugs for targeting anaerobic pathogens and certain tumor cells. Also employed in research for prodrug development, where selective activation in low-oxygen environments enhances therapeutic specificity.

Used as an intermediate in the synthesis of nitroimidazole-based pharmaceuticals, particularly in the development of antimicrobial and antiparasitic agents. Its structure supports the formation of bioreductive compounds that are active under hypoxic conditions, making it valuable in designing drugs for targeting anaerobic pathogens and certain tumor cells. Also employed in research for prodrug development, where selective activation in low-oxygen environments enhances therapeutic specificity.

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