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Structure of 1639444-93-1
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This brominated pyrrolopyridine scaffold features a sterically accessible C3 methyl group and a reactive bromine at the C4 position, enabling efficient cross-coupling transformations. The electron-deficient heteroaromatic core supports robust functionalization in palladium-catalyzed reactions under standard conditions.
4-Bromo-3-methyl-1H-pyrrolo[2,3-c]pyridine serves as a versatile building block for the synthesis of biologically active heterocycles. Its bromine and methyl groups enable directed functionalization via Pd-catalyzed cross-coupling and electrophilic substitution. The scaffold exhibits good bench stability and compatibility with standard synthetic workflows, facilitating efficient access to complex pyrrolopyridine-based intermediates in medicinal chemistry and materials science.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: