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Structure of 40314-71-4
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4,6-Dichloropicolinonitrile features a pyridine core bearing two chlorine substituents at the 4- and 6-positions and a nitrile group at C-3. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling direct coupling reactions under mild conditions. The dichloro substitution pattern enhances reactivity in nucleophilic aromatic substitution processes, while the nitrile moiety provides a versatile handle for downstream functionalization.
4,6-Dichloropicolinonitrile serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via nucleophilic substitution and metal-catalyzed coupling reactions. The dichloro substituents provide orthogonal reactivity for sequential functionalization, while the nitrile group offers a handle for hydrolysis or reduction. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: