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Structure of 1421341-09-4
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This boronate reagent features a pyridine core functionalized with a tert-butoxy group and a tetramethyl-1,3,2-dioxaborolane moiety. The electron-deficient pyridine ring enhances coupling efficiency in palladium-catalyzed cross-coupling reactions. The dioxaborolane unit provides excellent stability and compatibility under standard conditions, enabling reliable C–C bond formation in complex molecular architectures.
2-(Tert-butoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The tert-butoxy group enhances solubility and stability, while the pinacol boronate moiety enables reliable coupling under mild conditions. This reagent exhibits excellent functional group tolerance and bench stability, facilitating efficient construction of biaryl scaffolds and heterocyclic frameworks 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: