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Structure of 851759-19-8
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Methyl 6-chloro-2-methylnicotinate is a halogenated pyridine ester featuring a chlorinated C6 position and a methyl-substituted C2 carbon. This electron-deficient heterocycle integrates readily into synthetic sequences requiring steric bulk and polarized ring systems. The methyl ester group enables direct derivatization or hydrolysis to the corresponding acid, facilitating downstream functionalization in medicinal chemistry and agrochemical development under standard conditions.
Methyl 6-chloro-2-methylnicotinate serves as a versatile building block in the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-substituted pyridine core enables directed functionalization, while the methyl ester group facilitates selective transformations. The 6-chloro substituent provides a handle for palladium-catalyzed cross-coupling reactions, and the 2-methyl group enhances stability and influences regioselectivity. This compound exhibits excellent bench stability and is compatible with standard purification methods, making it well-suited for iterative synthetic workflows in medicinal chemistry and process development.
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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: