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Structure of 480424-93-9
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N-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide features a boronate ester group flanked by tetramethylcyclopentadienone rings, providing exceptional stability under standard conditions. This bench-stable reagent integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation with aryl halides. The acetamide moiety enhances solubility and facilitates downstream functionalization in synthetic workflows.
N-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pinacol boronate group enables stable, bench-ready handling and orthogonal reactivity under mild conditions. It facilitates efficient C–C bond formation with aryl halides and triflates, making it ideal for constructing biaryl scaffolds in medicinal chemistry and materials science. Functional group tolerance supports integration into 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: