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Structure of 86308-26-1
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2-Hexyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane offers enhanced stability and solubility in organic media, enabling efficient Suzuki-Miyaura coupling reactions. The bulky tetramethyl substitution minimizes protodeboronation, while the hexyl chain improves compatibility with nonpolar solvents. This boronate ester delivers reliable performance under standard conditions.
2-Hexyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent for Suzuki-Miyaura cross-coupling reactions. Its sterically protected dioxaborolane ring enhances shelf life and minimizes protodeboronation, while the hexyl group provides solubility in organic media. Functions reliably in diverse coupling protocols with aryl, heteroaryl, and vinyl halides, enabling efficient C–C bond formation under standard 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: