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Structure of 171364-81-1
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This boronate ester integrates a phenyl ketone moiety with a stable tetramethyl-1,3,2-dioxaborolane group, enabling efficient Suzuki-Miyaura coupling under standard conditions. The electron-deficient arylboronate facilitates rapid cross-coupling, while the bench-stable, moisture-tolerant structure simplifies handling and storage in synthetic workflows.
1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanone serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. Its stable boronate ester functionality enables efficient C–C bond formation under mild conditions, with excellent functional group tolerance and bench stability. The acetyl group provides orthogonal reactivity for downstream modifications, making it ideal for constructing complex aryl ketone scaffolds in medicinal chemistry and materials synthesis.
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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: