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Structure of 1207370-28-2
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2(1H)-one integrates a boronate ester handle at the 6-position of a quinolin-2(1H)-one scaffold, enabling efficient Suzuki-Miyaura coupling. This bench-stable reagent combines enhanced solubility with predictable reactivity, streamlining access to functionalized quinoline derivatives in medicinal chemistry and materials synthesis.
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2(1H)-one serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. The quinolin-2(1H)-one core provides a stable, functionalized heterocyclic scaffold with demonstrated utility in medicinal chemistry and materials science. Bench-stable and readily purified, it facilitates efficient late-stage diversification via Suzuki-Miyaura coupling, enabling rapid access to complex molecular architectures.
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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: