4-(4-Bromophenyl)pyridine

98%

Reagent Code: #145385
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CAS Number 39795-60-3

science Other reagents with same CAS 39795-60-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.09 g/mol
Formula C₁₁H₈BrN
thermostat Physical Properties
Boiling Point 318.7°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in materials science for the preparation of organic semiconductors and ligands in catalysis. The bromine functionality enables easy functionalization via palladium-catalyzed reactions such as Suzuki or Heck couplings, enhancing its utility in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿180.00
inventory 1g
10-20 days ฿790.00
inventory 5g
10-20 days ฿3,800.00

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4-(4-Bromophenyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in materials science for the preparation of organic semiconductors and ligands in catalysis. The bromine functionality enables easy functionalization via palladium-catalyzed reactions such as Su

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in materials science for the preparation of organic semiconductors and ligands in catalysis. The bromine functionality enables easy functionalization via palladium-catalyzed reactions such as Suzuki or Heck couplings, enhancing its utility in research and industrial applications.

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