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Structure of 870067-55-3
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1-Benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one is a bench-stable boronate ester featuring a pyridinone core and a benzyl group at the 1-position. This compound integrates readily into Suzuki-Miyaura coupling reactions under standard conditions, enabling efficient C–C bond formation with aryl halides. The tetramethyl-1,3,2-dioxaborolane moiety enhances stability and reactivity, while the para-substituted pyridinone scaffold provides directional control in cross-coupling processes.
1-Benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pyridin-2(1H)-one core provides enhanced stability and functional group compatibility, while the pinacol boronate moiety enables efficient coupling under mild conditions. Bench-stable and readily purified by flash chromatography, it facilitates the construction of biaryl scaffolds common in medicinal chemistry and materials science.
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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: