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Structure of 959244-28-1
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2,5-Dibromoisonicotinaldehyde features a pyridine core bearing bromine substituents at the 2 and 5 positions, enhancing electrophilicity at the aldehyde carbon. This electron-deficient scaffold enables efficient coupling in cross-coupling reactions and serves as a key building block for functionalized heterocycles in medicinal chemistry and materials science.
2,5-Dibromoisonicotinaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of brominated heterocyclic scaffolds via coupling and cyclization reactions. Its aldehyde functionality facilitates efficient derivatization, while the strategically positioned bromine atoms support palladium-catalyzed cross-coupling processes. The compound exhibits good bench stability and is readily purified by column chromatography, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: