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Structure of 181365-26-4
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under standard conditions. The tert-butyl carbamate-protected indole scaffold offers enhanced stability and solubility, facilitating handling and purification in synthetic workflows.
(1-(tert-Butoxycarbonyl)-1H-indol-3-yl)boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. The Boc-protected indole moiety ensures excellent functional group tolerance and compatibility with diverse reaction conditions, enabling efficient construction of biologically relevant indole-containing scaffolds. Its crystalline form and ease of purification facilitate reliable handling in multi-step synthesis.
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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: