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Structure of 42521-09-5
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Methyl 2,6-dichloroisonicotinate is a bench-stable, electron-deficient heterocyclic ester featuring two chlorine substituents at the 2- and 6-positions of the pyridine ring. This configuration enhances reactivity in cross-coupling processes and facilitates incorporation into pharmaceutical intermediates. The methyl ester group enables straightforward derivatization under standard conditions.
Methyl 2,6-dichloroisonicotinate serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its electron-deficient pyridine core enables efficient Suzuki-Miyaura and Buchwald-Hartwig couplings, while the ester functionality supports selective hydrolysis or derivatization. The ortho-dichloro substitution enhances reactivity in nucleophilic aromatic substitution and provides synthetic handles for further functionalization. Bench-stable and readily purified by flash chromatography, it functions reliably in multi-step syntheses of heterocyclic scaffolds and API intermediates.
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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: