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Structure of 1392210-94-4
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3-Bromoimidazo[1,2-a]pyridine-7-carbonitrile features a brominated imidazopyridine core paired with a nitrile group at the 7-position, enabling direct functionalization in cross-coupling reactions. The electron-deficient heterocycle facilitates palladium-catalyzed transformations, while the nitrile moiety provides a handle for downstream derivatization. This scaffold offers high stability under standard reaction conditions and is well-suited for medicinal chemistry applications requiring rigid, polarizable frameworks.
3-Bromoimidazo[1,2-a]pyridine-7-carbonitrile serves as a versatile building block for constructing bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions due to its dual reactive handles: the bromide at C3 and the nitrile at C7. Its stability under standard synthetic conditions and compatibility with diverse functional groups facilitate efficient access to imidazo[1,2-a]pyridine-based scaffolds relevant to medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501
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Lot numbers can be found on the outside label of a product: