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Structure of 463336-62-1
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2-Bromo-6-(1H-imidazol-1-yl)pyridine features a bromine atom at the 2-position and a pendant imidazole group at the 6-position of the pyridine ring. This configuration enables efficient coupling in transition metal-catalyzed reactions, particularly in C–N bond formation. The molecule combines electrophilic reactivity with robust heterocyclic stability, facilitating its use in medicinal chemistry and materials synthesis.
2-Bromo-6-(1H-imidazol-1-yl)pyridine serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. Its bromine moiety enables palladium-catalyzed cross-coupling reactions with broad functional group tolerance, while the imidazole group provides a rigid, polar handle suitable for hydrogen bonding in medicinal chemistry applications. The compound exhibits bench stability and facilitates efficient synthesis of pyridine-based pharmaceutical intermediates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: