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Structure of 25240-59-9
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This boronate moiety integrates readily into cross-coupling reactions under mild conditions. Featuring exceptional bench stability and moisture tolerance, it enables efficient C–C bond formation in complex molecular architectures.
4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-ol serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its high functional group tolerance and low toxicity facilitate reliable C–C bond formation under mild conditions. The tetramethyl substitution enhances stability and solubility in common organic solvents, simplifying purification and handling in synthetic workflows.
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GHS Pictogram :
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GHS No : GHS07,GHS08
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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-H361
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: