5-Amino-2-iodopyridine

≥95%

Reagent Code: #136960
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CAS Number 29958-12-1

science Other reagents with same CAS 29958-12-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.01 g/mol
Formula C₅H₅IN₂
badge Registry Numbers
MDL Number MFCD02706663
thermostat Physical Properties
Boiling Point 331.8°C
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

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 targeted drug candidates. Commonly employed in cross-coupling reactions due to the presence of the iodine moiety, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the preparation of agrochemicals and functional materials where nitrogen-containing heterocycles are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿690.00
inventory 1g
10-20 days ฿2,270.00
inventory 5g
10-20 days ฿7,430.00
inventory 25g
10-20 days ฿31,430.00

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5-Amino-2-iodopyridine
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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 targeted drug candidates. Commonly employed in cross-coupling reactions due to the presence of the iodine moiety, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the preparation of agrochemicals and funct

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 targeted drug candidates. Commonly employed in cross-coupling reactions due to the presence of the iodine moiety, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the preparation of agrochemicals and functional materials where nitrogen-containing heterocycles are required.

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