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Structure of 21635-92-7
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4-Methylpyridine-2,6-dicarbonitrile features a pyridine core with two nitrile groups at the 2 and 6 positions and a methyl substituent at the 4 position. This electron-deficient heterocycle integrates readily into modular synthesis pathways, offering high stability under standard conditions. The strategic placement of functional groups enables efficient coupling in transition metal-catalyzed reactions and facilitates incorporation into advanced ligands and pharmaceutical intermediates.
4-Methylpyridine-2,6-dicarbonitrile serves as a versatile building block in synthetic organic chemistry, enabling the construction of functionalized heterocyclic scaffolds through established coupling and cyclization protocols. Its dual nitrile groups and methyl-substituted pyridine core provide high reactivity in nucleophilic substitution and transition-metal-catalyzed transformations, offering excellent functional group tolerance and bench stability for use in medicinal chemistry and materials science applications.
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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 : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: