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Structure of 121247-01-6
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2-(3-Fluorophenyl)-2-oxoacetaldehyde features a reactive aldehyde group flanked by a fluorinated phenyl ring, enabling selective conjugation in synthetic transformations. This electron-deficient carbonyl system facilitates efficient imine formation and serves as a key intermediate in the construction of bioactive heterocycles under mild conditions.
2-(3-Fluorophenyl)-2-oxoacetaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds via condensation and cyclization reactions. Its α-keto aldehyde functionality offers high reactivity in nucleophilic addition processes, while the ortho-fluoro substituent provides moderate electronic modulation and enhanced metabolic stability. The compound exhibits sufficient bench stability for handling under standard laboratory conditions and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process development workflows.
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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: