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Structure of 39891-04-8
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5-Fluoronicotinaldehyde features a fluorinated pyridine ring with an aldehyde group at the 5-position, enabling selective conjugation in synthetic transformations. This electron-deficient heterocycle integrates readily into bioactive scaffolds and serves as a key intermediate in medicinal chemistry applications.
5-Fluoronicotinaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to heterocyclic scaffolds and bioactive molecules. Its aldehyde functionality reacts readily with amines, hydrazines, and nucleophiles under mild conditions, facilitating the construction of imines, hydrazones, and cyclic derivatives. The fluorine substituent enhances metabolic stability and modulates electronic properties, making it valuable for medicinal chemistry applications. Bench-stable and amenable to standard purification techniques, 5-Fluoronicotinaldehyde is well-suited for high-throughput synthesis and process development workflows.
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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: