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

≥95%

Reagent Code: #198539
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CAS Number 1249877-11-9

science Other reagents with same CAS 1249877-11-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.09 g/mol
Formula C₁₀H₈BrFN₂
badge Registry Numbers
MDL Number MFCD14647516
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antifungal agents and kinase inhibitors. Its structure supports the creation of bioactive molecules by serving as a building block in multi-step organic reactions. Commonly employed in medicinal chemistry for modifying benzyl-imidazole scaffolds to enhance binding affinity and selectivity in drug candidates. Also utilized in agrochemical research for designing new active ingredients with improved stability and biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,810.00
1-(2-bromo-4-fluorobenzyl)-1H-imidazole
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antifungal agents and kinase inhibitors. Its structure supports the creation of bioactive molecules by serving as a building block in multi-step organic reactions. Commonly employed in medicinal chemistry for modifying benzyl-imidazole scaffolds to enhance binding affinity and selectivity in drug candidates. Also utilized in agrochemical research for designing new active ingredients with improved stab

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antifungal agents and kinase inhibitors. Its structure supports the creation of bioactive molecules by serving as a building block in multi-step organic reactions. Commonly employed in medicinal chemistry for modifying benzyl-imidazole scaffolds to enhance binding affinity and selectivity in drug candidates. Also utilized in agrochemical research for designing new active ingredients with improved stability and biological activity.

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