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Structure of 1025707-93-0
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This boronate ester features a dihydropyran-6-yl moiety that enables selective coupling in Suzuki-Miyaura reactions. The tetramethyl-substituted dioxaborolane ring provides exceptional stability and moisture tolerance, facilitating handling under standard conditions. Ideal for integrating oxygenated heterocycles into complex molecular architectures.
2-(3,4-Dihydro-2H-pyran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura coupling reactions. The dihydropyran moiety provides orthogonal functionality and facilitates downstream transformations in complex molecule synthesis. Its high functional group tolerance and ease of purification make it ideal for iterative cross-coupling strategies in medicinal chemistry and natural product synthesis.
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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: