2-Iodopyridin-4-amine

95%

Reagent Code: #200606
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CAS Number 88511-26-6

science Other reagents with same CAS 88511-26-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.01 g/mol
Formula C₅H₅IN₂
badge Registry Numbers
MDL Number MFCD08235121
thermostat Physical Properties
Melting Point 99 °C
Boiling Point 350.5±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.055±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating drug candidates targeting cancer and inflammatory diseases. Also employed in cross-coupling reactions, such as Suzuki and Heck reactions, to build complex heterocyclic systems in agrochemicals and materials science. The iodine moiety facilitates metal-catalyzed transformations, enhancing its utility in modern synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,290.00
inventory 250mg
10-20 days ฿14,580.00
inventory 1g
10-20 days ฿23,330.00
2-Iodopyridin-4-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating drug candidates targeting cancer and inflammatory diseases. Also employed in cross-coupling reactions, such as Suzuki and Heck reactions, to build complex heterocyclic systems in agrochemicals and materials science. The iodine moiety facilita

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating drug candidates targeting cancer and inflammatory diseases. Also employed in cross-coupling reactions, such as Suzuki and Heck reactions, to build complex heterocyclic systems in agrochemicals and materials science. The iodine moiety facilitates metal-catalyzed transformations, enhancing its utility in modern synthetic routes.

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