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Structure of 1264193-11-4
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6-Bromopyrazolo[1,5-a]pyridine features a bromine substituent at the 6-position of a fused pyrazolo[1,5-a]pyridine core, providing a reactive handle for palladium-catalyzed cross-coupling transformations. The electron-deficient heteroaromatic framework enables efficient incorporation into bioactive scaffolds and functional materials. This bench-stable compound serves as a key intermediate in synthetic medicinal chemistry and advanced materials development.
6-Bromopyrazolo[1,5-a]pyridine serves as a versatile building block for the synthesis of heterocyclic scaffolds in medicinal chemistry and catalytic cross-coupling reactions. The bromine substituent enables reliable Suzuki, Stille, or Buchwald–Hartwig coupling transformations, facilitating the construction of biaryl and complex nitrogen-containing frameworks. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical choice for iterative synthesis and library generation.
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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-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: