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Structure of 741709-58-0
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This boronate-functional pyridyl ketone integrates readily into cross-coupling reactions, offering a stable, bench-ready platform for constructing complex heteroaryl architectures. The tetramethylboronate moiety enables efficient Suzuki-Miyaura coupling, while the acetyl group provides a handle for further derivatization.
1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)ethanone serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. The pyridyl ketone moiety enables efficient functionalization at the 4-position, while the stable tetramethylboronate group facilitates mild reaction conditions, excellent functional group tolerance, and straightforward purification—making it ideal for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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: