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Structure of 212127-80-5
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This boronate ester features a 2,5-dihydrofuran-3-yl group integrated via a stable dioxaborolane scaffold. The structure combines enhanced stability with efficient coupling performance in Suzuki-Miyaura reactions. Ideal for constructing complex heterocyclic architectures under mild conditions.
2-(2,5-Dihydrofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The 2,5-dihydrofuran moiety provides a versatile handle for late-stage functionalization in heterocyclic synthesis, with excellent functional group tolerance and predictable reactivity. Its tetramethyl-substituted dioxaborolane ring ensures high chemical stability and ease of purification, making it ideal for iterative coupling strategies in medicinal chemistry and process development.
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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: