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Structure of 1638847-77-4
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Methyl 2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate delivers a boronate ester functionality paired with an electron-deficient aryl fluorine for efficient Suzuki-Miyaura coupling. This bench-stable reagent integrates seamlessly into C–C bond formation workflows, enabling rapid access to substituted biaryl architectures under standard conditions.
Methyl 2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The ortho-fluorine substituent enables directed metalation and facilitates subsequent functionalization, while the pinacol boronate group offers excellent bench stability, ease of handling, and broad functional group tolerance. It functions reliably in the construction of biaryl motifs and complex heterocyclic scaffolds under standard catalytic conditions.
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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: