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Structure of 1511732-68-5
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5-Bromo-1H-thieno[2,3-c]pyrazole features a fused thienopyrazole core with a bromine substituent at the 5-position, delivering enhanced reactivity for cross-coupling transformations. The electron-deficient heterocycle integrates readily into pharmaceutical scaffolds and functional materials, offering high stability under standard conditions.
5-Bromo-1H-thieno[2,3-c]pyrazole serves as a versatile heterocyclic building block for medicinal chemistry and materials science. The bromine substituent enables palladium-catalyzed cross-coupling reactions, facilitating the construction of biaryl and extended π-conjugated systems. Its fused thienopyrazole core exhibits excellent bench stability and functional group tolerance, supporting efficient derivatization in standard synthetic workflows.
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Lot numbers can be found on the outside label of a product: