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Structure of 113118-82-4
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5-Chloronicotinaldehyde delivers a reactive aldehyde group flanked by a chlorine substituent on a pyridine ring, enabling direct incorporation into heterocyclic scaffolds. This bench-stable, moisture-tolerant reagent facilitates efficient synthesis of bioactive intermediates and functionalized ligands under standard conditions.
5-Chloronicotinaldehyde serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling the construction of heterocyclic scaffolds via condensation and coupling reactions. Its aldehyde functionality offers high reactivity in nucleophilic additions, while the chlorine substituent provides orthogonal handle for palladium-catalyzed cross-couplings. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in API development.
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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-H317-H319
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: