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Structure of 1788044-15-4
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Methyl 5-methylpyridazine-3-carboxylate features a pyridazine core with strategically positioned methyl and ester groups, enabling direct incorporation into heterocyclic scaffolds. This bench-stable compound serves as a key intermediate in the synthesis of bioactive molecules, particularly where electron-deficient nitrogen-rich systems are required.
Methyl 5-methylpyridazine-3-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridazine-based heterocycles. Its methyl and ester functionalities offer orthogonal reactivity for downstream modifications, including hydrolysis, nucleophilic substitution, and transition-metal-catalyzed coupling reactions. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in API development.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: