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Structure of 65169-38-2
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2-Chloro-4-methylnicotinonitrile features a sterically accessible nitrile group flanked by a chlorine substituent and a methyl moiety on the pyridine ring, enabling direct functionalization in late-stage diversification. This electron-deficient scaffold integrates readily into synthetic intermediates for pharmaceuticals and agrochemicals under standard conditions.
2-Chloro-4-methylnicotinonitrile serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds via cross-coupling and nucleophilic substitution reactions. Its ortho-chloro and cyano groups provide complementary reactivity for late-stage functionalization, while the methyl group enhances metabolic stability. Bench-stable and amenable to purification by recrystallization or chromatography, it facilitates scalable synthesis of bioactive heterocycles.
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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: