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Structure of 1255309-13-7
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is a bench-stable boronate ester featuring a planar carbazole core with enhanced solubility and compatibility in cross-coupling reactions. The tetramethylcyclopentadienone moiety enables efficient palladium-catalyzed coupling under standard conditions, delivering conjugated heteroaryl architectures with high functional group tolerance.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole serves as a versatile boronate building block in palladium-catalyzed cross-coupling reactions. Its carbazole core provides structural rigidity and electron-rich character, enabling efficient coupling with aryl, heteroaryl, and vinyl halides. The pinacol boronate group offers excellent stability, ease of handling, and compatibility with diverse reaction conditions, making it ideal for constructing complex scaffolds in medicinal chemistry and materials science applications.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: