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Structure of 532967-21-8
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2,6-Difluoro-4-hydroxybenzaldehyde features a strategically positioned aldehyde group flanked by two fluorine atoms and a phenolic hydroxyl, enabling direct functionalization in synthetic routes. The electron-withdrawing fluorines enhance electrophilicity at the carbonyl center while the hydroxyl group provides a handle for derivatization. This combination delivers high reactivity under mild conditions, facilitating efficient coupling reactions in pharmaceutical intermediates and specialty materials synthesis.
2,6-Difluoro-4-hydroxybenzaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated aromatic scaffolds. The ortho-fluorine substituents enhance metabolic stability and modulate electronic properties, while the aldehyde and phenolic hydroxyl groups provide orthogonal handles for downstream functionalization via condensation, coupling, or derivatization reactions. Bench-stable and compatible with standard synthetic workflows, it facilitates the construction of complex heterocycles and bioactive molecules.
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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: