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Structure of 2908-71-6
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5-(Bromomethyl)-2-methylpyrimidin-4-amine hydrobromide features a reactive bromomethyl group at the 5-position, enabling efficient coupling in nucleophilic substitution reactions. The pyrimidine core provides a stable, electron-deficient platform for functionalization. This bench-stable salt facilitates direct incorporation into bioconjugation workflows and small molecule synthesis under standard conditions.
5-(Bromomethyl)-2-methylpyrimidin-4-amine hydrobromide serves as a versatile building block for the synthesis of biologically active heterocycles. The bromomethyl group enables efficient nucleophilic substitution, while the pyrimidine core provides a stable scaffold for further functionalization. Its bench-stable nature and compatibility with common coupling reactions facilitate straightforward incorporation into medicinal chemistry campaigns and API development workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P264-P270-P271-P280-P304+P340-P330-P331-P363-P501
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Lot numbers can be found on the outside label of a product: