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Structure of 1113049-90-3
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6-Chloro-5-(trifluoromethyl)nicotinaldehyde delivers a potent electron-deficient heteroaromatic scaffold ideal for cross-coupling and condensation reactions. The trifluoromethyl group enhances lipophilicity and metabolic stability, while the chloro substituent enables further functionalization. This bench-stable aldehyde integrates readily into complex molecular architectures under standard conditions.
6-Chloro-5-(trifluoromethyl)nicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via condensation and coupling reactions. Its electron-deficient pyridine core supports diverse functionalization, while the aldehyde group facilitates facile derivatization. Bench-stable and compatible with standard purification methods, it functions effectively in multistep syntheses requiring high regiochemical control and functional group tolerance.
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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: