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Structure of 1046812-03-6
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This boronate ester features a dihydrofuran-containing moiety, offering enhanced stability and reactivity in cross-coupling applications. The tetramethyl-substituted dioxaborolane ring ensures excellent shelf life and moisture tolerance, enabling reliable use under standard conditions.
2-(4,5-Dihydrofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. The dihydrofuran moiety provides orthogonal reactivity and structural diversity in heterocyclic synthesis, while the tetramethyl-substituted dioxaborolane enhances air stability and simplifies purification. It functions reliably in late-stage functionalization and is compatible with diverse reaction conditions across medicinal chemistry and materials science applications.
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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-P271-P280
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Lot numbers can be found on the outside label of a product: