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Structure of 63131-29-3
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Methyl 4-fluorobenzoylacetate features a fluorinated aromatic ring coupled to a β-keto ester moiety, enabling direct integration into conjugated systems. This bench-stable compound serves as a key building block for synthesizing fluorinated pharmaceutical intermediates and functionalized polymers under standard conditions.
Methyl 4-fluorobenzoylacetate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted benzene rings and heterocyclic scaffolds. Its α-keto ester functionality facilitates nucleophilic addition, condensation reactions, and Michael additions under mild conditions. The fluorine substituent imparts enhanced metabolic stability and modulates electronic properties, making it valuable for medicinal chemistry applications. Bench-stable and readily purified by distillation or chromatography, it functions effectively in multi-step syntheses requiring functional group tolerance and predictable reactivity.
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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: