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*For research and further manufacturing use only, not for direct human use.
Structure of 196212-27-8
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This boronate-functionalized benzene derivative features two tetramethyl-1,3,2-dioxaborolane groups at the 1,3-positions, enabling efficient Suzuki-Miyaura cross-coupling reactions. The sterically shielded dioxaborolane moieties enhance stability under ambient conditions while maintaining high reactivity in palladium-catalyzed transformations. Ideal for constructing complex biaryl architectures with precise spatial control.
1,3-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene serves as a versatile bisboronate building block for Suzuki-Miyaura cross-coupling reactions. Its ortho-diboryl substitution enables efficient construction of biaryl and polyaryl architectures with high regiocontrol. The sterically protected boronate groups exhibit excellent stability under ambient conditions, facilitating handling and purification. This reagent functions reliably in diverse coupling protocols, supporting scalable synthesis of complex scaffolds relevant to pharmaceutical and materials research.
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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: