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Structure of 958358-00-4
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5-Bromo-6-methyl-1H-pyrrolo[2,3-b]pyridine features a fused heterocyclic core with bromine and methyl substituents at strategic positions, enabling direct functionalization in cross-coupling reactions. This electron-deficient scaffold integrates readily into pharmaceutical intermediates and advanced materials, offering enhanced reactivity and stability under standard conditions.
5-Bromo-6-methyl-1H-pyrrolo[2,3-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and catalytic cross-coupling applications. The bromo group enables reliable Suzuki, Stille, and Negishi couplings, while the methyl substituent enhances solubility and modulates electronic properties. Bench-stable and readily purified by flash chromatography, it functions effectively in the synthesis of biologically active scaffolds and functionalized polycycles.
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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: