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Structure of 89281-13-0
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2,6-Dichloroisonicotinamide features a pyridine core with strategically positioned chlorine atoms at the 2 and 6 positions, enhancing electrophilicity at the carbonyl carbon. This electron-deficient scaffold facilitates direct incorporation into heterocyclic systems, serving as a key intermediate in medicinal chemistry for targeted kinase inhibitors and bioactive compound synthesis under standard conditions.
2,6-Dichloroisonicotinamide serves as a versatile building block in medicinal chemistry, enabling the construction of heterocyclic scaffolds through direct coupling and functionalization. Its ortho-chlorine substituents facilitate palladium-catalyzed cross-coupling reactions, while the amide group provides hydrogen-bonding capability and metabolic stability. The compound exhibits excellent bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthesis campaigns 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 : H302-H315-H332-H335
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Precautionary Statements : P261-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: