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Structure of 911113-15-0
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6-Bromoimidazo[1,2-a]pyridine-8-carbonitrile features a rigid heteroaromatic core with complementary electron-withdrawing nitrile and bromide substituents. This combination enables direct functionalization in cross-coupling reactions and facilitates integration into bioactive scaffolds requiring defined electronic properties. The molecule exhibits high stability under standard reaction conditions.
6-Bromoimidazo[1,2-a]pyridine-8-carbonitrile serves as a versatile building block for constructing bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. The bromo and nitrile groups provide orthogonal handles for sequential derivatization, facilitating the synthesis of complex scaffolds relevant to medicinal chemistry and agrochemical development. Its bench-stable crystalline form simplifies handling and purification in multi-step syntheses.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: