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Structure of 754131-60-7
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3-Bromo-2-(bromomethyl)pyridine features a bromomethyl group flanked by a pyridine ring and a bromine at the 3-position, enabling dual electrophilic reactivity. This bifunctional scaffold integrates readily into synthetic sequences requiring orthogonal functionalization, particularly in medicinal chemistry and heterocyclic derivatization workflows.
3-Bromo-2-(bromomethyl)pyridine serves as a versatile bifunctional building block in synthetic chemistry, enabling efficient construction of pyridine-based heterocycles and pharmaceutical intermediates. The bromomethyl group facilitates nucleophilic substitution and Suzuki-type coupling reactions, while the 3-bromo substituent supports palladium-catalyzed cross-coupling. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for iterative synthesis workflows in medicinal chemistry and process 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: