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Structure of 1436608-93-3
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2-Fluoro-4-nitrophenylboronic acid features a boronate moiety flanked by electron-withdrawing fluorine and nitro groups, enhancing its reactivity in Suzuki-Miyaura couplings. The para-nitro substitution stabilizes the boronic acid under standard conditions while enabling selective functionalization. This bench-stable reagent integrates readily into complex molecule synthesis with high chemoselectivity.
2-Fluoro-4-nitrophenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The ortho-fluoro and para-nitro substituents provide orthogonal reactivity, allowing sequential functionalization in complex molecule synthesis. Its bench-stable nature and compatibility with diverse reaction partners make it well-suited for pharmaceutical and agrochemical intermediate development.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: