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Structure of 1000341-51-4
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5-Bromo-1H-pyrrolo[3,2-b]pyridine features a fused heterocyclic core with a bromine substituent at the 5-position, enabling direct functionalization in cross-coupling reactions. This electron-deficient scaffold integrates readily into pharmaceutical and agrochemical scaffolds, offering high reactivity under standard Pd-catalyzed conditions. The molecule exhibits excellent stability and solubility in common organic solvents, facilitating use in process-scale synthesis.
5-Bromo-1H-pyrrolo[3,2-b]pyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-established bromine reactivity. The molecule exhibits good bench stability and functional group tolerance, facilitating efficient incorporation into complex scaffolds. Its fused pyrrolopyridine core provides structural rigidity and electron-deficient character, making it particularly valuable for constructing bioactive molecules and pharmaceutical intermediates via standard coupling protocols.
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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: