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Structure of 193481-62-8
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2-(Dimethylamino)-6-fluoronicotinaldehyde features a fluorinated pyridine core paired with a dimethylamino group, delivering enhanced electron density at the para-position. This combination enables efficient coupling in transition-metal-catalyzed transformations and facilitates rapid conjugation in bioconjugate chemistry. The aldehyde functionality provides direct reactivity for imine formation and oxime ligation, supported by bench-stable handling under standard conditions.
2-(Dimethylamino)-6-fluoronicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of fluorinated heterocycles and bioactive scaffolds. Its electron-rich dimethylamino group enhances reactivity in nucleophilic additions, while the aldehyde functionality facilitates imine formation and condensation reactions. Bench-stable and compatible with standard purification methods, it functions effectively in multistep syntheses requiring functional group tolerance and predictable regiochemistry.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: