2-Chloro-5-iodo-4-pyridinamine

≥95%

Reagent Code: #116500
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CAS Number 800402-12-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.46 g/mol
Formula C₅H₄ClIN₂
badge Registry Numbers
MDL Number MFCD09834661
thermostat Physical Properties
Boiling Point 367.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique combination of halogen atoms makes it particularly valuable in cross-coupling reactions, such as the Suzuki and Sonogashira reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and agrochemicals. Additionally, the presence of both chlorine and iodine atoms allows for selective functionalization, enabling researchers to tailor the molecule for specific applications. In medicinal chemistry, it is often employed as a building block for the synthesis of potential drug candidates, particularly those targeting neurological disorders and infectious diseases. Its role in the creation of heterocyclic compounds also makes it significant in the development of new materials with potential applications in electronics and optoelectronics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿504.00
inventory 5g
10-20 days ฿3,816.00
inventory 1g
10-20 days ฿1,278.00
inventory 10g
10-20 days ฿6,354.00
2-Chloro-5-iodo-4-pyridinamine
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique combination of halogen atoms makes it particularly valuable in cross-coupling reactions, such as the Suzuki and Sonogashira reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and agrochemicals. Additionally, the presence of both chlorine and iodine atoms allows for selective functionalization, enabling researchers to tailor the molecule for specific applications. In medicinal chemistry, it is often employed as a building block for the synthesis of potential drug candidates, particularly those targeting neurological disorders and infectious diseases. Its role in the creation of heterocyclic compounds also makes it significant in the development of new materials with potential applications in electronics and optoelectronics.
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