4-Bromo-1-(3-bromophenyl)-1H-imidazole

97%

Reagent Code: #155714
fingerprint
CAS Number 1363253-98-8

science Other reagents with same CAS 1363253-98-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.97 g/mol
Formula C₉H₆Br₂N₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the creation of complex heterocyclic compounds that interact with biological targets such as enzymes and receptors. Commonly employed in medicinal chemistry for building blocks in drug discovery due to the bromine positions allowing further functionalization via cross-coupling reactions like Suzuki or Heck reactions. Also utilized in research settings to develop new imidazole-based bioactive molecules with potential antimicrobial and anti-inflammatory properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,370.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Bromo-1-(3-bromophenyl)-1H-imidazole
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the creation of complex heterocyclic compounds that interact with biological targets such as enzymes and receptors. Commonly employed in medicinal chemistry for building blocks in drug discovery due to the bromine positions allowing further functionalization via cross-coupling reactions like Suzuki or Heck reactions. Also utilized in research settings

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the creation of complex heterocyclic compounds that interact with biological targets such as enzymes and receptors. Commonly employed in medicinal chemistry for building blocks in drug discovery due to the bromine positions allowing further functionalization via cross-coupling reactions like Suzuki or Heck reactions. Also utilized in research settings to develop new imidazole-based bioactive molecules with potential antimicrobial and anti-inflammatory properties.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...