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Structure of 1123169-25-4
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6-Bromo-2-methylpyridazin-3(2H)-one features a brominated pyridazinone core with a methyl group at the 2-position, offering a sterically accessible site for cross-coupling and functionalization. This bench-stable heterocycle integrates readily into medicinal chemistry campaigns, serving as a building block for bioactive molecules requiring electron-deficient aromatic systems.
6-Bromo-2-methylpyridazin-3(2H)-one serves as a versatile heterocyclic building block for medicinal chemistry and process development. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the pyridazinone core offers hydrogen-bonding capacity and metabolic stability. The 2-methyl group enhances solubility and modulates electronic properties. This compound exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in standard coupling and functionalization 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-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: