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Structure of 76006-13-8
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3-Bromo-1H-pyrazolo[3,4-c]pyridine features a fused heterocyclic core with a bromine substituent at the 3-position, enabling direct functionalization in cross-coupling reactions. This electron-deficient scaffold integrates readily into bioactive molecule synthesis, offering enhanced stability and predictable reactivity under standard conditions.
3-Bromo-1H-pyrazolo[3,4-c]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. The bromine substituent enables efficient palladium-catalyzed cross-coupling reactions, facilitating the construction of biaryl and aryl-substituted scaffolds. Its stability under standard reaction conditions and compatibility with diverse functional groups make it well-suited for modular synthesis workflows in API development and advanced material design.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: