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Structure of 1310384-28-1
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This boronate moiety integrates a protected indole scaffold with two flanking chlorine atoms, enabling selective cross-coupling under standard conditions. The tert-butyl carbamate group ensures stability and orthogonal handling, while the electron-deficient aryl boronic acid facilitates efficient Suzuki-Miyaura reactions in complex molecular architectures.
(1-(tert-Butoxycarbonyl)-5,6-dichloro-1H-indol-2-yl)boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura coupling reactions. The Boc-protected indole nitrogen enables orthogonal functionalization, while the dichloro substitution pattern enhances regioselectivity in downstream transformations. Its compatibility with aqueous conditions and tolerance to diverse reaction partners make it ideal for constructing complex heterocyclic scaffolds in medicinal chemistry and materials 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: