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Structure of 1370633-67-2
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Methyl 6-chloro-4-methylpyridazine-3-carboxylate features a sterically hindered pyridazine core with complementary electron-withdrawing and donating substituents, enabling efficient coupling in late-stage functionalization. The methyl ester group facilitates direct derivatization under standard conditions, while the chlorine atom serves as a reliable handle for nucleophilic substitution. This compound exhibits excellent bench stability and solubility in common organic solvents, streamlining its integration into synthetic workflows.
Methyl 6-chloro-4-methylpyridazine-3-carboxylate serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions and nucleophilic substitution at the C6 chlorine site. The methyl and ester functionalities offer orthogonal reactivity, facilitating further derivatization in medicinal chemistry and process development. Bench-stable and readily purified by column chromatography, it functions efficiently in standard synthetic workflows.
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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: