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Structure of 1427382-24-8
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6-Bromo-7-methylpyrazolo[1,5-a]pyridine features a fused heterocyclic core with bromine and methyl substituents at distinct positions, enabling selective functionalization. The electron-deficient pyrazolopyridine scaffold supports efficient cross-coupling reactions under standard conditions, while the steric profile of the 7-methyl group enhances regioselectivity in palladium-catalyzed transformations. This bench-stable compound serves as a key building block for bioactive molecule synthesis.
6-Bromo-7-methylpyrazolo[1,5-a]pyridine serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo functionality. The methyl group at the 7-position enhances regiochemical control and improves solubility in organic media. This compound functions effectively in Suzuki-Miyaura and Stille couplings, facilitating efficient access to substituted pyrazolopyridine scaffolds relevant to medicinal chemistry and materials science.
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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: