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Structure of 131773-48-3
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2-Chloroimidazo[1,2-a]pyridine-3-carbonitrile is a heterocyclic building block featuring a chlorinated imidazopyridine core with a nitrile handle. This electron-deficient scaffold integrates readily into medicinal chemistry campaigns, offering high reactivity in cross-coupling and nucleophilic substitution reactions. The molecule's planar structure and polar functional groups enhance solubility in common organic solvents while maintaining bench stability under standard conditions.
2-Chloroimidazo[1,2-a]pyridine-3-carbonitrile serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to imidazopyridine-based scaffolds. Its dual functionality—reactive chloro group and nitrile handle—facilitates palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The compound exhibits excellent bench stability and compatibility with diverse functional groups, supporting scalable synthesis of bioactive molecules.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: