5-Bromo-1-phenyl-1H-benzo[d]imidazole

97%

Reagent Code: #146129
fingerprint
CAS Number 221636-18-6

science Other reagents with same CAS 221636-18-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.13 g/mol
Formula C₁₃H₉BrN₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. The bromine substituent at the 5-position facilitates further functionalization through cross-coupling reactions, such as copper- or palladium-catalyzed couplings with aryl or heteroaryl groups, to construct more complex benzimidazole derivatives. It serves as a building block in medicinal chemistry for biologically active molecules due to its benzimidazole core with N-phenyl substitution, which is known for interacting with various enzymes and receptors. Commonly employed in research for designing kinase inhibitors, antimicrobial compounds, and anti-inflammatory agents. Also utilized in the preparation of fluorescent probes for biochemical assays owing to its favorable photophysical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,130.00
inventory 1g
10-20 days ฿1,230.00
inventory 5g
10-20 days ฿9,750.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Bromo-1-phenyl-1H-benzo[d]imidazole
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. The bromine substituent at the 5-position facilitates further functionalization through cross-coupling reactions, such as copper- or palladium-catalyzed couplings with aryl or heteroaryl groups, to construct more complex benzimidazole derivatives. It serves as a building block in medicinal chemistry for biologically active molecules due to its benzimidazole core with N-ph

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. The bromine substituent at the 5-position facilitates further functionalization through cross-coupling reactions, such as copper- or palladium-catalyzed couplings with aryl or heteroaryl groups, to construct more complex benzimidazole derivatives. It serves as a building block in medicinal chemistry for biologically active molecules due to its benzimidazole core with N-phenyl substitution, which is known for interacting with various enzymes and receptors. Commonly employed in research for designing kinase inhibitors, antimicrobial compounds, and anti-inflammatory agents. Also utilized in the preparation of fluorescent probes for biochemical assays owing to its favorable photophysical 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...