2-Chloro-5-iodo-4-methylpyridine
97%
Reagent
Code: #116464
CAS Number
550347-54-1
blur_circular Chemical Specifications
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Molecular Information
Weight
253.47 g/mol
Formula
C₆H₅ClIN
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Registry Numbers
MDL Number
MFCD13185454
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Physical Properties
Boiling Point
279.4±35.0°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 construction of more complex molecules. Its unique structure, featuring both chloro and iodo substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the methyl group can influence the reactivity and selectivity of the compound, enabling the synthesis of specific target molecules with high precision. It is also employed in the preparation of heterocyclic compounds, which are often key components in medicinal chemistry due to their biological activity.
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2-Chloro-5-iodo-4-methylpyridine
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the construction of more complex molecules. Its unique structure, featuring both chloro and iodo substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the methyl group can influence the reactivity and selectivity of the compound, enabling the synthesis of specific target molecules with high precision. It is also employed in the preparation of heterocyclic compounds, which are often key components in medicinal chemistry due to their biological activity.
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