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Structure of 425702-91-6
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6-Bromo-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one is a bench-stable heterocyclic scaffold featuring a bromine substituent at the 6-position and a lactam functionality at C3. This electron-deficient triazolopyridinone core enables direct coupling in transition-metal-catalyzed transformations, facilitating rapid access to diverse bioactive compounds in medicinal chemistry and chemical biology applications.
6-Bromo-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one serves as a versatile heterocyclic building block for medicinal chemistry and catalytic cross-coupling applications. The bromine substituent enables palladium-catalyzed coupling reactions with broad functional group tolerance, while the triazolopyridinone core provides structural rigidity and hydrogen-bonding capacity. Bench-stable and readily purified, it facilitates efficient synthesis of complex scaffolds relevant to kinase inhibitors and other bioactive molecules.
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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: