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Structure of 477252-29-2
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2-(6-Bromopyridin-3-yl)propan-2-ol features a brominated pyridine ring appended to a tertiary alcohol scaffold, delivering a bench-stable, moisture-tolerant building block for C–C coupling reactions. The sterically hindered hydroxyl group facilitates selective functionalization, while the electron-deficient pyridine moiety enables efficient transition-metal catalyzed transformations. This compound integrates seamlessly into complex molecular architectures under standard conditions.
2-(6-Bromopyridin-3-yl)propan-2-ol serves as a versatile building block for C–C bond formation via palladium-catalyzed cross-coupling reactions. Its tertiary alcohol functionality enhances bench stability and simplifies purification, while the bromopyridine moiety enables reliable Suzuki, Stille, and Negishi couplings. This structure functions as a key intermediate in the synthesis of biologically active heterocycles and pharmaceutical scaffolds.
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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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: