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Structure of 954240-46-1
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4-Bromo-6-methylpyridazin-3(2H)-one features a brominated pyridazinone core with a methyl group at the 6-position, offering a sterically hindered, electron-deficient heterocyclic scaffold. This structure enables direct coupling in late-stage functionalization and serves as a robust building block for medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
4-Bromo-6-methylpyridazin-3(2H)-one serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridazinone scaffolds. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the lactam functionality offers hydrogen-bonding capacity and metabolic stability. The methyl group enhances lipophilicity and provides steric control in downstream transformations. This compound exhibits excellent bench stability, simplifies purification, and functions reliably in standard synthetic workflows for 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-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: