2-(3-Nitrophenyl)imidazole

95%

Reagent Code: #173055
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CAS Number 13682-18-3

science Other reagents with same CAS 13682-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.17 g/mol
Formula C₉H₇N₃O₂
badge Registry Numbers
MDL Number MFCD05863370
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with biological activity. It serves in the preparation of compounds exhibiting antifungal, antiparasitic, and anticancer properties. Also employed in the creation of ligands for metal-catalyzed reactions and in the design of functional materials due to its nitrogen-rich structure. Its nitro group allows for further chemical modifications, making it valuable in medicinal chemistry research and drug discovery processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,090.00
inventory 250mg
10-20 days ฿3,040.00
inventory 1g
10-20 days ฿4,580.00
inventory 5g
10-20 days ฿21,130.00
inventory 10g
10-20 days ฿42,250.00

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2-(3-Nitrophenyl)imidazole
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with biological activity. It serves in the preparation of compounds exhibiting antifungal, antiparasitic, and anticancer properties. Also employed in the creation of ligands for metal-catalyzed reactions and in the design of functional materials due to its nitrogen-rich structure. Its nitro group allows for further chemical modifications, making it valuable in medicinal chemistry research

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of imidazole-based drugs with biological activity. It serves in the preparation of compounds exhibiting antifungal, antiparasitic, and anticancer properties. Also employed in the creation of ligands for metal-catalyzed reactions and in the design of functional materials due to its nitrogen-rich structure. Its nitro group allows for further chemical modifications, making it valuable in medicinal chemistry research and drug discovery processes.

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