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Structure of 269410-21-1
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-ol features a boronate ester group conjugated to a naphthol scaffold, enabling efficient Suzuki-Miyaura coupling under mild conditions. The tetramethyl-substituted dioxaborolane enhances stability and resistance to hydrolysis, while the phenolic OH facilitates directional functionalization. This bench-stable reagent integrates readily into complex molecule assembly workflows.
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-ol serves as a versatile boronate building block for Suzuki-Miyaura coupling, enabling efficient C–C bond formation under mild conditions. Its naphthol functionality offers enhanced stability and facilitates orthogonal functional group handling. The pinacol boronate moiety ensures excellent bench stability, ease of purification, and compatibility with diverse reaction partners, making it ideal for constructing complex heterocyclic scaffolds and advanced API intermediates in medicinal chemistry and materials science 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-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: