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Structure of 801303-22-0
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2-Amino-5-fluoronicotinonitrile features a fluorinated pyridine core bearing both amino and nitrile functionalities, enabling integration into diverse heterocyclic scaffolds. The electron-deficient ring facilitates nucleophilic substitution, while the amino group offers direct derivatization potential. This bench-stable reagent streamlines access to bioactive nitrogen-rich architectures in medicinal chemistry.
2-Amino-5-fluoronicotinonitrile serves as a versatile building block in medicinal chemistry, enabling the synthesis of fluorinated heterocycles and kinase inhibitor scaffolds. Its ortho-difunctionalized pyridine core facilitates efficient coupling reactions and transition-metal-catalyzed transformations. The amino and nitrile groups offer complementary reactivity for derivatization, while the fluorine substituent enhances metabolic stability and bioavailability. This compound exhibits excellent bench stability and is readily purified by recrystallization, making it ideal for high-throughput screening and process-scale synthesis.
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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: