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Structure of 1256785-53-1
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Methyl 2-chloro-5-cyanonicotinate is a versatile heterocyclic building block featuring a chlorinated pyridine core with orthogonal functional groups. The cyano and ester moieties enable sequential derivatization, while the chlorine atom facilitates palladium-catalyzed cross-coupling reactions. This compound exhibits stability under standard conditions and integrates readily into synthetic sequences requiring electron-deficient aromatic scaffolds.
Methyl 2-chloro-5-cyanonicotinate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds. The ortho-chloro and cyano groups provide complementary reactivity for palladium-catalyzed cross-coupling and nucleophilic substitution, while the ester functionality supports hydrolysis or reduction. Bench-stable and readily purified by flash chromatography, it facilitates robust, scalable routes to medicinally relevant core structures.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: