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Structure of 65202-52-0
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Methyl 6-bromopyridazine-3-carboxylate features a bromine substituent at the 6-position of a pyridazine core, enabling direct functionalization in cross-coupling reactions. The ester group facilitates selective derivatization and enhances solubility in polar organic solvents. This bench-stable heterocycle serves as a key intermediate in medicinal chemistry for constructing nitrogen-rich scaffolds.
Methyl 6-bromopyridazine-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-established bromo functionality. The ester group provides a handle for selective transformations, while the pyridazine core offers compatibility with diverse functional groups. Its bench-stable nature and predictable reactivity facilitate efficient construction of complex scaffolds in medicinal chemistry and materials science applications.
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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: