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Structure of 928653-80-9
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tert-Butyl 5-bromo-1H-pyrrolo[2,3-b]pyridine-1-carboxylate features a brominated pyrrolopyridine core with a bench-stable tert-butyl ester handle. This electrophilic scaffold enables direct coupling in cross-coupling reactions, facilitating rapid access to complex heterocycles. The electron-deficient aryl bromide integrates cleanly into Pd-catalyzed transformations under standard conditions.
tert-Butyl 5-bromo-1H-pyrrolo[2,3-b]pyridine-1-carboxylate serves as a versatile building block for the synthesis of substituted pyrrolopyridine scaffolds. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the tert-butyl ester group offers stability and convenient deprotection under mild acidic conditions. This compound facilitates efficient access to biologically relevant heterocycles in medicinal chemistry and materials science applications.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: