3-Amino-4-iodopyridine

98%

Reagent Code: #134982
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CAS Number 105752-11-2

science Other reagents with same CAS 105752-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.01 g/mol
Formula C₅H₅IN₂
badge Registry Numbers
MDL Number MFCD04971334
thermostat Physical Properties
Melting Point 69.2-69.5°C
inventory_2 Storage & Handling
Density 2.055
Storage Room temperature

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. Also employed in the preparation of agrochemicals and in research for labeling or probing applications due to the presence of both amino and iodo groups, which facilitate coupling reactions and molecular modifications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,220.00
inventory 5g
10-20 days ฿4,820.00
3-Amino-4-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. Also employed in the preparation of agrochemicals and in research for labeling or probing applications due to the presence of both amino and iodo groups, which facilitate coupling reactions and molecular modification

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. Also employed in the preparation of agrochemicals and in research for labeling or probing applications due to the presence of both amino and iodo groups, which facilitate coupling reactions and molecular modifications.

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