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Structure of 180287-02-9
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This methyl ester derivative features a fluorinated alkyl chain adjacent to a ketone and ester functional group, enabling precise manipulation in synthetic transformations. The electron-withdrawing fluorine enhances reactivity at the α-carbon, facilitating enolization and nucleophilic addition reactions under mild conditions. This bench-stable compound serves as a key building block for complex heterocycles and bioactive molecule synthesis.
2-Fluoro-3-oxopentanoic acid methyl ester serves as a versatile building block in synthetic organic chemistry, enabling efficient access to fluorinated carbonyl intermediates. Its α-fluoro ketone functionality facilitates stereoselective transformations and acts as a key precursor in the construction of bioactive heterocycles and fluorinated pharmaceutical scaffolds. The methyl ester group enhances bench stability and simplifies purification, while the conjugated enone system supports diverse Michael additions and cyclization reactions under standard conditions.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: