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Structure of 1563177-30-9
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5-Bromo-2-methyl-2H-pyrazolo[4,3-b]pyridine features a brominated pyrazolopyridine core with a methyl group at the 2-position, offering a robust scaffold for medicinal chemistry. The electron-deficient heterocycle facilitates transition-metal-catalyzed coupling reactions, while the bench-stable structure enables reliable integration into complex molecular architectures under standard conditions.
5-Bromo-2-methyl-2H-pyrazolo[4,3-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and catalytic cross-coupling applications. Its bromo group enables reliable Suzuki, Stille, or Negishi coupling reactions, while the methyl substituent enhances solubility and modulates electronic properties. The pyrazolopyridine core exhibits bench stability and compatibility with diverse reaction conditions, facilitating efficient access to complex scaffolds in API discovery 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: