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Structure of 884494-96-6
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6-Fluoro-2-methylnicotinaldehyde delivers a strategically positioned fluorine atom and methyl group on the nicotinaldehyde scaffold, enabling precise tuning of electronic properties and steric profile. This configuration enhances reactivity in coupling processes and supports efficient incorporation into bioactive heterocycles under standard conditions.
6-Fluoro-2-methylnicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of bioactive heterocycles. Its ortho-methyl and meta-fluoro substituents provide enhanced reactivity and metabolic stability, facilitating downstream functionalization via nucleophilic addition, condensation, or coupling reactions. The aldehyde group offers high synthetic versatility for amine-based conjugation, imine formation, and scaffold diversification. Bench-stable and readily purified, it supports scalable synthesis workflows in API development.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: