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Structure of 1033202-51-5
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5-Fluoro-3-nitropicolinonitrile features a trifunctional pyridine core bearing fluorine, nitro, and cyano groups in strategic ortho positions. This electron-deficient scaffold enables direct integration into heterocyclic architectures via nucleophilic substitution or transition-metal-catalyzed coupling. The molecule exhibits enhanced stability under standard bench conditions and facilitates rapid assembly of complex nitrogen-rich frameworks for medicinal chemistry and materials applications.
5-Fluoro-3-nitropicolinonitrile serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds. Its strategic placement of fluorine, nitro, and cyano groups supports sequential functionalization via nucleophilic substitution, reduction, and cyclization reactions. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic campaigns in medicinal chemistry and process development.
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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: