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Structure of 1246761-84-1
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B-1H-Pyrrolo[2,3-b]pyridin-4-ylboronic acid features a heteroaryl boronic acid moiety integrated into a fused pyrrolopyridine scaffold. This configuration imparts enhanced stability and reactivity in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The electron-deficient nature of the ring system promotes selective coupling with diverse aryl halides.
B-1H-Pyrrolo[2,3-b]pyridin-4-ylboronic acid serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. Its boronic acid functionality enables efficient Suzuki-Miyaura cross-coupling reactions under mild conditions, facilitating the synthesis of complex arylated derivatives with high regioselectivity. The compound exhibits good bench stability and compatibility with diverse functional groups, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
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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: