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Structure of 50844-89-8
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Pyrimidine-4,6-dicarbonitrile features two nitrile groups positioned at the 4 and 6 ring carbons, creating a highly electron-deficient heterocyclic scaffold. This configuration enhances its utility in nucleophilic substitution reactions and as a building block for conjugated materials. The molecule exhibits robust stability under standard conditions and integrates readily into functionalized architectures.
Pyrimidine-4,6-dicarbonitrile serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidines via nucleophilic addition and condensation reactions. Its dual nitrile groups provide high reactivity for functionalization under mild conditions, facilitating the construction of complex scaffolds relevant to pharmaceutical and agrochemical development. The compound exhibits excellent bench stability and is readily purified by recrystallization, making it well-suited for routine laboratory use in medicinal chemistry and process research.
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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: