2,3-Dichloro-4-iodopyridine

95%

Reagent Code: #171374
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CAS Number 889865-45-6

science Other reagents with same CAS 889865-45-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.89 g/mol
Formula C₅H₂Cl₂IN
thermostat Physical Properties
Melting Point 109-113°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogen substituents allow for selective cross-coupling reactions, making it valuable in constructing complex pyridine-based molecules. Commonly employed in Suzuki and Buchwald-Hartwig reactions to form carbon-carbon and carbon-nitrogen bonds. Also utilized in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿1,120.00
inventory 25g
10-20 days ฿4,750.00
inventory 100g
10-20 days ฿18,640.00
inventory 500g
10-20 days ฿75,070.00

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2,3-Dichloro-4-iodopyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogen substituents allow for selective cross-coupling reactions, making it valuable in constructing complex pyridine-based molecules. Commonly employed in Suzuki and Buchwald-Hartwig reactions to form carbon-carbon and carbon-nitrogen bonds. Also utilized in the preparation of kinase inhibitors and other biologically active compounds in medicina

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogen substituents allow for selective cross-coupling reactions, making it valuable in constructing complex pyridine-based molecules. Commonly employed in Suzuki and Buchwald-Hartwig reactions to form carbon-carbon and carbon-nitrogen bonds. Also utilized in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research.

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