1-(2-Nitrophenyl)-1H-imidazole

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Reagent Code: #219803
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CAS Number 23309-16-2

science Other reagents with same CAS 23309-16-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.18 g/mol
Formula C₉H₇N₃O₂
badge Registry Numbers
MDL Number MFCD01795851
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the formation of nitrogen-containing heterocycles, which are common in bioactive molecules. It has been investigated in the synthesis of kinase inhibitors and antimicrobial agents due to its ability to participate in metal-catalyzed coupling reactions and cycloadditions. Also employed in photochemistry research as a nitroaromatic compound with light-responsive properties, useful in designing photo-labile protecting groups or sensors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,930.00
inventory 1g
10-20 days ฿10,020.00
inventory 5g
10-20 days ฿36,390.00

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1-(2-Nitrophenyl)-1H-imidazole
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the formation of nitrogen-containing heterocycles, which are common in bioactive molecules. It has been investigated in the synthesis of kinase inhibitors and antimicrobial agents due to its ability to participate in metal-catalyzed coupling reactions and cycloadditions. Also employed in photochemistry research as a nitroaromatic compound with light-responsive

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the formation of nitrogen-containing heterocycles, which are common in bioactive molecules. It has been investigated in the synthesis of kinase inhibitors and antimicrobial agents due to its ability to participate in metal-catalyzed coupling reactions and cycloadditions. Also employed in photochemistry research as a nitroaromatic compound with light-responsive properties, useful in designing photo-labile protecting groups or sensors.

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