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Structure of 2043962-01-0
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-ol features a boronate ester group attached to a naphthalene scaffold bearing a phenolic hydroxyl. This configuration enables direct coupling in Suzuki-Miyaura reactions with high functional group tolerance and stability under standard conditions. The tetramethyl-substituted dioxaborolane enhances shelf life and minimizes protodeboronation.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-ol serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The naphthol functionality enables direct C–O bond formation and facilitates downstream derivatization, while the stable tetramethylboronate group ensures excellent bench handling, air tolerance, and compatibility with diverse reaction conditions. Functions effectively in both small-molecule synthesis and functionalized heterocycle construction.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: