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Structure of 1934533-59-1
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5-Bromo-6-methyl-2H-pyrazolo[3,4-b]pyridine features a fused heterocyclic core with bromo and methyl substituents enabling direct functionalization in cross-coupling reactions. This bench-stable scaffold integrates readily into medicinal chemistry libraries, offering enhanced solubility and metabolic stability for target-oriented synthesis.
5-Bromo-6-methyl-2H-pyrazolo[3,4-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the methyl substituent enhances solubility and modulates electronic properties. The scaffold exhibits bench stability and compatibility with standard synthetic protocols, facilitating efficient access to complex pyrazolopyridine derivatives.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: