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Structure of 2446617-95-2
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This boronate-functionalized dihydroquinolinone integrates seamlessly into cross-coupling reactions under mild conditions. The tetramethyl-1,3,2-dioxaborolane moiety enables efficient Suzuki-Miyaura coupling, while the lactam core provides structural rigidity and enhanced solubility in polar organic solvents.
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate moiety enables stable, bench-ready handling and broad functional group tolerance. It facilitates efficient C–C bond formation with aryl, heteroaryl, and vinyl halides under standard catalytic conditions, enabling rapid access to substituted quinolinone scaffolds commonly found in medicinal chemistry and agrochemical research.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: