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Structure of 1235342-53-6
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3-(Bromomethyl)-5-methylpyridine hydrobromide features a reactive bromomethyl group flanked by an electron-deficient pyridine ring and a methyl substituent, enabling efficient coupling in nucleophilic substitution reactions. This bench-stable salt delivers reliable functionality in synthetic pathways requiring selective alkylation under mild conditions.
3-(Bromomethyl)-5-methylpyridine hydrobromide serves as a versatile electrophilic building block for C–H functionalization and heterocyclic synthesis. The bromomethyl group enables efficient alkylation reactions under mild conditions, while the pyridine nitrogen provides inherent directing capability and enhanced solubility in polar media. This compound exhibits good bench stability and facilitates straightforward purification, making it suitable for iterative synthetic sequences in medicinal chemistry and process development.
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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 : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: