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Structure of 1316852-65-9
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5-Bromo-2-methyl-2H-pyrazolo[3,4-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 cross-coupling reactions and integrates readily into bioactive molecules. This bench-stable compound serves as a key intermediate in targeted synthesis workflows.
5-Bromo-2-methyl-2H-pyrazolo[3,4-b]pyridine serves as a versatile building block for the synthesis of biologically active heterocycles. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the methyl substituent enhances stability and modulates electronic properties. The scaffold is well-suited for constructing complex pyrazolopyridine frameworks found in pharmaceutical intermediates, offering excellent bench stability and compatibility with standard synthetic protocols.
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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-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: