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Structure of 2068065-16-5
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6-Bromo-4-hydroxypyrazolo[1,5-a]pyridine-3-carbonitrile features a fused heterocyclic core with complementary functional groups enabling direct derivatization. The bromo substituent facilitates cross-coupling reactions, while the hydroxyl and nitrile moieties offer sites for conjugation or metal coordination. This scaffold demonstrates stability under standard conditions and compatibility with diverse synthetic transformations.
6-Bromo-4-hydroxypyrazolo[1,5-a]pyridine-3-carbonitrile serves as a versatile building block for constructing bioactive heterocycles, enabling direct functionalization at the 4-position via cross-coupling or nucleophilic substitution. The bromo and nitrile groups offer orthogonal reactivity, facilitating late-stage diversification in medicinal chemistry. Bench-stable and amenable to purification by chromatography or recrystallization, it functions effectively in Suzuki-Miyaura, Buchwald-Hartwig, and Ullmann-type transformations.
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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-H319
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: