4,7-Dibromo-1-methyl-1H-benzo[d]imidazole

95%

Reagent Code: #180283
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CAS Number 1235442-60-0

science Other reagents with same CAS 1235442-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.95 g/mol
Formula C₈H₆Br₂N₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity such as antifungal, antibacterial, and anticancer agents. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of complex molecules through cross-coupling reactions like Suzuki or Heck reactions. Also employed in materials science for designing organic semiconductors and fluorescent dyes due to its electron-rich aromatic framework. Commonly utilized in research settings for the preparation of ligands in catalysis and in the development of metal-organic frameworks (MOFs).

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,370.00
inventory 250mg
10-20 days ฿5,710.00
inventory 1g
10-20 days ฿18,860.00

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4,7-Dibromo-1-methyl-1H-benzo[d]imidazole
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity such as antifungal, antibacterial, and anticancer agents. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of complex molecules through cross-coupling reactions like Suzuki or Heck reactions. Also employed in materials science for designing organic semiconductors and fluorescent dyes due to its electron-rich ar

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity such as antifungal, antibacterial, and anticancer agents. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of complex molecules through cross-coupling reactions like Suzuki or Heck reactions. Also employed in materials science for designing organic semiconductors and fluorescent dyes due to its electron-rich aromatic framework. Commonly utilized in research settings for the preparation of ligands in catalysis and in the development of metal-organic frameworks (MOFs).

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