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Structure of 1217500-54-3
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This boronate moiety integrates a tert-butyl-protected pyrazole ring, offering a bench-stable, moisture-tolerant platform for C–C coupling reactions. The electron-deficient pyrazole core enables selective cross-coupling under mild conditions, while the Boc group provides orthogonal protection.
(1-(tert-Butoxycarbonyl)-1H-pyrazol-5-yl)boronic acid serves as a stable, bench-ready building block for the construction of pyrazole-containing scaffolds in medicinal chemistry and materials science. Its boronic acid functionality enables efficient Suzuki-Miyaura coupling under mild conditions, while the tert-butoxycarbonyl group provides orthogonal protection for subsequent amine derivatization. The compound exhibits excellent stability, facilitates straightforward purification, and functions reliably in multi-step syntheses requiring functional group tolerance and compatibility with diverse reaction conditions.
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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: