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Structure of 1788062-13-4
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5-Fluoro-2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine features a boronate ester group enabling efficient Suzuki-Miyaura coupling under mild conditions. The electron-deficient pyridine core enhances reactivity, while the tetramethyl-substituted dioxaborolane ensures stability and ease of handling. This compound integrates readily into complex molecular architectures with high functional group tolerance.
5-Fluoro-2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. The pyridine core enables access to biologically relevant heterocycles, while the tetramethylboronate group offers excellent stability, mild reaction conditions, and broad functional group tolerance. This reagent facilitates efficient C–C bond formation in medicinal chemistry and materials synthesis workflows.
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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: