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Structure of 2417489-94-0
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2,6-Difluoro-4-iodonicotinaldehyde features a highly reactive aldehyde group flanked by electron-withdrawing fluorine and iodine substituents, enhancing electrophilicity for efficient coupling in cross-coupling and bioconjugation workflows. The para-iodo substitution enables palladium-catalyzed transformations, while the ortho-fluorines improve metabolic stability and modulate electronic properties. This bench-stable reagent integrates readily into complex molecular architectures under standard conditions.
2,6-Difluoro-4-iodonicotinaldehyde serves as a versatile building block for the synthesis of fluorinated heterocycles and pharmaceutical intermediates. Its aldehyde functionality enables efficient nucleophilic additions and condensation reactions, while the ortho-fluoro and para-iodo substituents facilitate subsequent cross-coupling and electrophilic functionalization. The molecule exhibits good bench stability and compatibility with standard reaction conditions, supporting its use in multi-step synthetic sequences requiring orthogonal 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 : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: