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Structure of 31722-49-3
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1H-Imidazole-2-carbonitrile features a nitrogen-rich heterocyclic core paired with a reactive nitrile group, enabling direct incorporation into bioactive scaffolds. This bench-stable compound serves as a key building block for pharmaceutical intermediates and functional materials, leveraging its dual electronic and synthetic versatility in cross-coupling and cyclization reactions.
1H-Imidazole-2-carbonitrile serves as a versatile building block in medicinal chemistry, enabling efficient construction of imidazole-based scaffolds through nucleophilic addition and coupling reactions. Its nitrile group facilitates transformations to amides, amines, and carboxylic acids under standard conditions, while the imidazole core provides inherent hydrogen-bonding capacity and metabolic stability. Bench-stable and readily purified by recrystallization, it functions reliably in multistep syntheses for API development and functionalized heterocycle assembly.
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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: