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Structure of 785051-54-9
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This boronate-functionalized carbazole integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, offering robust stability under standard conditions. The tetramethyl-1,3,2-dioxaborolane moiety enables efficient C–C bond formation, while the electron-rich carbazole scaffold supports conjugated framework assembly in organic electronics and photoluminescent materials.
9-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. The carbazole core provides structural rigidity and electron-rich character, while the pinacol boronate group enables efficient Suzuki-Miyaura coupling under mild conditions. Bench-stable and compatible with diverse functional groups, it facilitates the construction of biaryl scaffolds in pharmaceutical and materials chemistry.
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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: