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Structure of 642494-37-9
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7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole integrates a stable boronate ester at the 7-position of indole, enabling efficient Suzuki-Miyaura cross-coupling under mild conditions. The tetramethyl dioxaborolane moiety enhances reactivity and shelf stability, while the electron-rich indole core supports diverse functionalization in medicinal chemistry and materials synthesis.
7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate group enables efficient C–C bond formation under mild conditions, with excellent stability during storage and handling. It functions reliably in the synthesis of biaryl scaffolds, particularly in constructing substituted indole derivatives used in pharmaceutical and agrochemical research.
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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: