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Structure of 38696-21-8
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5-Bromo-N,N-dimethylpyrimidin-2-amine features a brominated pyrimidine core with a dimethylamino group at the 2-position, enabling efficient coupling in cross-coupling reactions. The electron-rich amine moiety enhances reactivity, while the bromide serves as a robust handle for further functionalization. This compound exhibits excellent stability under standard bench conditions and is compatible with palladium-catalyzed transformations.
5-Bromo-N,N-dimethylpyrimidin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromo group at the 5-position. The N,N-dimethyl substitution enhances solubility and metabolic stability, while the pyrimidine core provides a rigid scaffold for targeted drug discovery. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient synthesis of complex heterocyclic architectures.
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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: