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Structure of 1000068-25-6
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This boronate moiety integrates a fluoroindole scaffold with a tert-butyl carbamate-protected amine, enabling stable coupling in Suzuki-Miyaura reactions. The electron-deficient arylboronic acid features enhanced shelf life and moisture tolerance, simplifying handling in synthetic workflows.
(1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. The Boc-protected indole core enables orthogonal functionalization in complex molecule synthesis, while the fluorine substituent enhances metabolic stability and modulates electronic properties. Its excellent functional group tolerance and ease of purification make it ideal for constructing pharmaceutically relevant indole scaffolds in medicinal chemistry workflows.
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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: