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Structure of 1193116-74-3
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5-Bromo-2-(bromomethyl)pyrimidine features a bromomethyl group at the 2-position and a bromine atom at the 5-position of the pyrimidine ring, enabling dual electrophilic reactivity. This bifunctional scaffold facilitates efficient coupling in nucleophilic substitution reactions, particularly in the synthesis of heterocyclic compounds and pharmaceutical intermediates under standard conditions.
5-Bromo-2-(bromomethyl)pyrimidine serves as a versatile di-functional building block in synthetic organic chemistry, enabling sequential functionalization at both the pyrimidine C5 and C2 positions. The bromomethyl group facilitates nucleophilic substitution reactions, while the C5-bromo substituent supports palladium-catalyzed cross-coupling processes. Its bench-stable nature and compatibility with standard protecting group strategies make it a practical reagent for constructing heterocyclic scaffolds relevant to medicinal chemistry and agrochemical development.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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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 : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: