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Structure of 42869-47-6
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6-Bromo-2-methyl-3H-imidazo[4,5-b]pyridine is a heterocyclic building block featuring a brominated imidazopyridine core with a methyl group at the 2-position. This scaffold offers enhanced reactivity in cross-coupling transformations due to its electron-deficient nature and steric profile. The molecule exhibits bench-stable handling characteristics and integrates readily into complex molecular architectures for medicinal chemistry and materials science applications.
6-Bromo-2-methyl-3H-imidazo[4,5-b]pyridine serves as a versatile building block for the synthesis of biologically active heterocycles, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo functionality. The methyl group enhances regioselectivity in further functionalization, while the imidazopyridine core provides structural rigidity and favorable pharmacophore properties. Bench-stable and compatible with standard purification methods, it facilitates efficient access to advanced intermediates in medicinal chemistry campaigns.
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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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: