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Structure of 214360-70-0
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This boronate ester features a thienyl group at the 2-position, enhancing electron density and enabling efficient cross-coupling in Suzuki-Miyaura reactions. The tetramethyl-substituted dioxaborolane ring imparts exceptional stability under ambient conditions, while maintaining high reactivity when activated. Ideal for constructing complex heteroaromatic architectures with minimal decomposition.
4,4,5,5-Tetramethyl-2-(3-thienyl)-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The thienyl group enables efficient incorporation into heteroaromatic scaffolds common in pharmaceuticals and materials science. Its tetramethyl substitution enhances reagent stability and simplifies purification, while the dioxaborolane ring facilitates reliable coupling under mild 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: