2-Chloro-5-iodo-4-pyridinamine
≥95%
Reagent
Code: #116500
CAS Number
800402-12-4
blur_circular Chemical Specifications
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Molecular Information
Weight
254.46 g/mol
Formula
C₅H₄ClIN₂
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Registry Numbers
MDL Number
MFCD09834661
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Physical Properties
Boiling Point
367.8°C at 760 mmHg
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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.
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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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