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Structure of 2504241-18-1
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[cd]indol-2(1H)-one features a boronate ester group enabling efficient Suzuki-Miyaura cross-coupling reactions. The fused indole core imparts structural rigidity and enhanced stability under standard conditions. This bench-stable reagent integrates seamlessly into complex molecular architectures, offering reliable functionalization in synthetic and medicinal chemistry workflows.
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[cd]indol-2(1H)-one serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. The tetramethylboronate group enables efficient Suzuki-Miyaura coupling under mild conditions, facilitating the construction of biaryl and heterobiaryl architectures. The benzo[cd]indol-2(1H)-one core provides a rigid, electron-deficient scaffold with established utility in medicinal chemistry and materials science. The compound exhibits excellent bench stability, minimal protodeboronation, and compatibility with diverse functional groups, enabling reliable incorporation into complex molecular frameworks.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: