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Structure of 942070-45-3
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tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate delivers a stable, bench-ready boronate handle for Suzuki-Miyaura cross-coupling. The tetramethyl-substituted dioxaborolane enhances reactivity and shelf stability, while the indole scaffold supports direct functionalization in complex molecule assembly.
tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate serves as a stable, bench-ready boron building block for palladium-catalyzed cross-coupling reactions. The indole core enables efficient access to functionalized heterocyclic scaffolds, while the Bpin group facilitates reliable Suzuki-Miyaura coupling under mild conditions. Its tert-butyl ester functionality offers orthogonal protection and simplifies purification, making it well-suited for iterative synthesis 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 : 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: