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Structure of 2102451-30-7
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This boronate moiety integrates readily into Suzuki-Miyaura couplings, delivering indole-based architectures with high functional group tolerance. The tert-butyl carbamate protection ensures stability during storage and handling, enabling straightforward deprotection to reveal the free amine under mild acidic conditions.
(1-(tert-Butoxycarbonyl)-1H-indol-4-yl)boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. The Boc-protected indole moiety enables orthogonal functionalization and facilitates purification, while the boronic acid group exhibits high reactivity with aryl halides under mild conditions. This compound is particularly valuable in constructing complex indole-containing scaffolds relevant to medicinal chemistry and materials science.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: