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Structure of 1448862-61-0
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Methyl 3-bromo-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine-2-carboxylate features a brominated tetrahydropyrazolopyridine core with a methyl ester handle, enabling direct incorporation into diverse synthetic sequences. The electron-deficient heterocyclic scaffold supports transition metal-catalyzed functionalization and serves as a key intermediate in the development of bioactive nitrogen-containing compounds.
Methyl 3-bromo-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine-2-carboxylate serves as a versatile building block for the synthesis of substituted pyrazolo[1,5-a]pyridine scaffolds. The bromine at C3 enables palladium-catalyzed cross-coupling reactions, while the ester group facilitates selective transformations and derivatization. Its bench-stable nature and compatibility with diverse functional groups support efficient route development in medicinal chemistry and process synthesis.
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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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: