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Structure of 89640-81-3
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Methyl 6-hydroxypyridazine-4-carboxylate features a pyridazine core bearing both hydroxyl and ester functionalities, enabling direct functionalization at the 6-position. This bench-stable derivative serves as a key intermediate in heterocyclic synthesis, particularly for bioactive molecule development. The electron-deficient ring facilitates nucleophilic substitution, while the hydroxyl group offers a handle for derivatization under mild conditions.
Methyl 6-hydroxypyridazine-4-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridazine-based heterocycles. The hydroxyl group facilitates direct functionalization or protection, while the ester moiety supports selective transformations and downstream derivatization. Its bench-stable nature and compatibility with standard coupling and reduction protocols make it ideal for modular synthesis of bioactive scaffolds.
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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-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: