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Structure of 101012-32-2
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2-Chloro-3-pyridineacetonitrile features a chlorinated pyridine core paired with a nitrile-bearing acetyl side chain, enabling direct incorporation into heterocyclic scaffolds. This bench-stable reagent facilitates efficient synthesis of bioactive pyridine derivatives through nucleophilic substitution and transition-metal-catalyzed coupling reactions.
2-Chloro-3-pyridineacetonitrile serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. Its dual functionality—reactive chloro group and electron-deficient nitrile—facilitates nucleophilic substitution, palladium-catalyzed coupling, and heterocycle elaboration under standard conditions. The compound exhibits good bench stability and compatibility with common protecting groups, facilitating purification and integration into multi-step syntheses.
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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: