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Structure of 156817-73-1
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This dibromo-imidazopyridine derivative features a saturated pyridine core with bromine atoms at the 2 and 3 positions, enabling direct functionalization in cross-coupling reactions. The tetrahydro structure enhances solubility and stability under standard conditions, while the imidazole nitrogen facilitates coordination in catalytic systems.
2,3-Dibromo-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine serves as a versatile building block for the synthesis of nitrogen-containing heterocycles, enabling efficient access to imidazo[1,2-a]pyridine scaffolds through palladium-catalyzed cross-coupling reactions. Its dibromo substitution pattern facilitates sequential functionalization, while the tetrahydro core offers enhanced stability and compatibility with standard synthetic workflows. The compound is bench-stable, readily purified by chromatography, and exhibits broad functional group tolerance, making it well-suited for medicinal chemistry and process development applications.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: