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Structure of 875293-89-3
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6-Chloro-5-methylpyridine-2-carbonitrile features a pyridine core functionalized with chlorine, methyl, and nitrile groups at strategic positions, enabling selective coupling in medicinal chemistry. The electron-deficient ring facilitates nucleophilic substitution, while the nitrile group serves as a handle for derivatization. This scaffold delivers enhanced metabolic stability and tunable lipophilicity in bioactive molecule design.
6-Chloro-5-methylpyridine-2-carbonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its orthogonal functionality—combining a chloropyridine, methyl group, and nitrile—enables diverse downstream transformations via nucleophilic substitution, metal-catalyzed coupling, and heterocycle elaboration. The molecule exhibits excellent bench stability and facilitates efficient purification, making it well-suited for multi-step synthetic sequences requiring functional group tolerance and predictable reactivity.
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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: