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Structure of 1415124-73-0
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Methyl 3,5-difluoro-4-formylbenzoate features a trifunctional aromatic core with electron-withdrawing fluorine substituents and a reactive formyl group. This bench-stable reagent integrates readily into synthetic sequences requiring electrophilic functionality or directed metalation. The ester moiety enables straightforward derivatization while maintaining compatibility with standard organic transformations.
Methyl 3,5-difluoro-4-formylbenzoate serves as a versatile building block in medicinal chemistry and materials science, enabling direct incorporation of ortho-fluorinated aromatic motifs with a reactive aldehyde handle. The formyl group facilitates nucleophilic additions, reductive aminations, and imine-based cyclizations, while the methyl ester supports selective transformations under standard conditions. Bench-stable and compatible with diverse reaction environments, it functions effectively in multi-step syntheses requiring fluorinated heterocycles or functionalized aryl scaffolds.
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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: