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Structure of 1809395-84-3
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4,5-Dibromo-3,6-dihydro-2-methyl-3,6-dioxo-1(2H)-pyridazineacetic acid features a dibrominated pyridazine core paired with a carboxylic acid side chain, enabling direct conjugation in synthetic workflows. The electron-deficient heterocycle facilitates nucleophilic addition reactions, while the acetic acid moiety supports derivatization and solubility modulation. This structure combines stability with reactive handles for advanced molecular design.
4,5-Dibromo-3,6-dihydro-2-methyl-3,6-dioxo-1(2H)-pyridazineacetic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyridazine scaffolds. Its dibromo functionality facilitates palladium-catalyzed cross-coupling reactions, while the acetic acid side chain offers a handle for derivatization and purification. Bench-stable and compatible with standard synthetic workflows, it functions effectively in medicinal chemistry and process 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-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: