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Structure of 1092563-66-0
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This boronate-functionalized pyrazole-piperidine ketone integrates seamlessly into Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate moiety enables efficient, palladium-catalyzed bond formation under mild conditions, while the sterically hindered piperidine scaffold enhances solubility and stability. Designed for streamlined synthesis of complex heterocyclic architectures in medicinal chemistry and materials science applications.
1-(4-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)piperidin-1-yl)ethan-1-one serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethyl-1,3,2-dioxaborolane moiety enables stable, room-temperature handling and high functional group tolerance. It facilitates efficient C–C bond formation with aryl and heteroaryl halides, enabling rapid diversification of pyrazole-containing piperidine 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: