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Structure of 14959-33-2
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6-Bromo-N,N-dimethylpyridazin-3-amine features a brominated pyridazine core with a dimethylamino group at the 3-position, offering a reactive handle for cross-coupling and a tunable nitrogen center. This bench-stable compound integrates readily into diverse heterocyclic architectures, enabling efficient access to functionalized pyridazine derivatives in medicinal chemistry and materials synthesis.
6-Bromo-N,N-dimethylpyridazin-3-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine electrophilicity and electron-deficient pyridazine core. The N,N-dimethyl substitution enhances solubility and metabolic stability while maintaining reactivity in standard Suzuki-Miyaura and Buchwald-Hartwig protocols. Its bench-stable crystalline form facilitates handling and purification, making it ideal for constructing complex heterocyclic scaffolds in 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: