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Structure of 1260666-12-3
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Ethyl 2-fluoro-4-pyridineacetate features a fluorinated pyridine ring paired with an ester-functionalized side chain, enabling direct incorporation into synthetic routes requiring electron-deficient heterocyclic motifs. This bench-stable intermediate integrates readily into cross-coupling and functionalization cascades, offering predictable reactivity under standard conditions.
Ethyl 2-fluoro-4-pyridineacetate serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated pyridine-containing scaffolds. Its ester functionality facilitates downstream transformations such as hydrolysis, reduction, or coupling reactions, while the ortho-fluoropyridine moiety provides enhanced metabolic stability and tunable electronic properties. The compound exhibits good bench stability and is compatible with standard synthetic protocols, making it valuable for the construction of bioactive heterocycles and API intermediates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: