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Structure of 374790-93-9
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This boronate ester features a 2-furanyl group integrated into a stable dioxaborolane scaffold, enabling efficient coupling in Suzuki-Miyaura reactions. The tetramethyl substitution enhances shelf life and resistance to hydrolysis, while the furan moiety provides a bioactive handle for pharmaceutical and agrochemical synthesis.
2-(2-Furanyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its furan-containing structure enables efficient incorporation into heteroaromatic scaffolds, with excellent functional group tolerance and predictable reactivity. The tetramethyl-substituted dioxaborolane enhances stability and simplifies purification, making it ideal for iterative synthesis workflows in medicinal chemistry and materials 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: