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Structure of 862129-81-5
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This boronate ester features a thiopyran-based heterocyclic scaffold that enhances solubility and stability under standard conditions. The tetramethyl-substituted dioxaborolane ring enables efficient Suzuki-Miyaura coupling, while the fused thiacycle offers unique electronic modulation for synthetic applications in medicinal chemistry and materials science.
2-(3,6-Dihydro-2H-thiopyran-4-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 thiopyran-containing moiety provides a versatile heterocyclic scaffold with predictable reactivity and excellent functional group tolerance. Its sterically protected boronate ester enables efficient coupling under mild conditions, facilitating the construction of complex molecular architectures in 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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: