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Structure of 2965-22-2
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Methyl 2-fluoro-5-nitrobenzenecarboxylate features a fluorinated aromatic ring paired with electron-withdrawing nitro and ester groups, enabling selective functionalization in synthetic transformations. This bench-stable reagent integrates readily into cross-coupling and nucleophilic substitution sequences under standard conditions.
Methyl 2-fluoro-5-nitrobenzenecarboxylate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the electron-deficient aromatic ring. The ortho-fluoro group facilitates nucleophilic aromatic substitution, while the nitro and ester functionalities offer complementary reactivity for downstream transformations. Its bench-stable nature and compatibility with standard coupling reactions make it ideal for constructing complex heterocyclic scaffolds and multi-functional 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: