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Structure of 1806511-07-8
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Ethyl 2-amino-5-fluoronicotinate features a fluorinated pyridine core with complementary amine and ester functionalities, enabling direct incorporation into heterocyclic scaffolds. The electron-deficient aromatic ring facilitates transition-metal-catalyzed coupling reactions, while the bench-stable amino group supports derivatization under mild conditions. This versatile building block streamlines access to bioactive nitrogen-containing compounds.
Ethyl 2-amino-5-fluoronicotinate serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocyclic scaffolds. Its amino and ester functionalities offer orthogonal reactivity for coupling, cyclization, and derivatization under standard conditions. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for multi-step 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: