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Structure of 98139-15-2
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4-Aminopyridine-2-carbonitrile features a pyridine ring bearing an amino group at the 4-position and a nitrile at the 2-position, creating a highly electron-deficient heterocycle. This dual functionality enables efficient coupling in synthetic transformations, particularly in medicinal chemistry scaffolds and functional materials. The compound exhibits good solubility in common organic solvents and stability under standard bench conditions.
4-Aminopyridine-2-carbonitrile serves as a versatile building block in medicinal chemistry, enabling the construction of heterocyclic scaffolds through its dual functionality: the nucleophilic amine and electrophilic nitrile groups. It facilitates efficient derivatization via amidation, cyclization, and transition-metal-catalyzed coupling reactions. The molecule exhibits good bench stability and is compatible with common purification methods, making it a practical choice for iterative synthesis campaigns targeting bioactive compounds.
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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: