4-bromo-2-(2-methoxyphenyl)-1H-imidazole

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Reagent Code: #197613
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CAS Number 1415562-37-6

science Other reagents with same CAS 1415562-37-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.10 g/mol
Formula C₁₀H₉BrN₂O
badge Registry Numbers
MDL Number MFCD22665887
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of imidazole-based drugs with biological activity. It serves in the preparation of antifungal, anticancer, and anti-inflammatory agents due to the imidazole core’s affinity for enzyme inhibition. The bromo substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex molecules in medicinal chemistry research. Also employed in the creation of ligands for metal-catalyzed reactions and in the study of structure-activity relationships in drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,330.00

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4-bromo-2-(2-methoxyphenyl)-1H-imidazole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of imidazole-based drugs with biological activity. It serves in the preparation of antifungal, anticancer, and anti-inflammatory agents due to the imidazole core’s affinity for enzyme inhibition. The bromo substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex molecules in medicinal chemistry research. Also e

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of imidazole-based drugs with biological activity. It serves in the preparation of antifungal, anticancer, and anti-inflammatory agents due to the imidazole core’s affinity for enzyme inhibition. The bromo substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex molecules in medicinal chemistry research. Also employed in the creation of ligands for metal-catalyzed reactions and in the study of structure-activity relationships in drug design.

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