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Structure of 1190321-20-0
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6-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid features a fused heterocyclic core with a bromo substituent at the 6-position and a carboxylic acid group at the 3-position, enabling direct coupling or derivatization. This configuration imparts enhanced reactivity for C–C and C–heteroatom bond formation in medicinal chemistry and materials synthesis. The molecule exhibits bench-stable handling characteristics and compatibility with standard cross-coupling protocols under mild conditions.
6-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid serves as a versatile building block for constructing bioactive heterocycles in medicinal chemistry. The molecule combines a brominated pyrrolopyridine core with a carboxylic acid handle, enabling direct coupling reactions and derivatization via amide formation or esterification. Its bench-stable nature and compatibility with Suzuki-Miyaura and Buchwald-Hartwig cross-couplings facilitate rapid access to functionalized analogs. This compound functions as a key intermediate in the synthesis of kinase inhibitors and other pharmaceutical scaffolds requiring fused nitrogen heterocycles.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: