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Structure of 1319591-26-8
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This trityl-protected pyrazolopyridine boronate integrates seamlessly into cross-coupling workflows, offering enhanced stability and selective reactivity. The tetramethylboronate moiety enables efficient Suzuki-Miyaura coupling, while the trityl group provides robust protection for downstream transformations under standard conditions.
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-trityl-1H-pyrazolo[3,4-b]pyridine serves as a robust boronate building block for palladium-catalyzed cross-coupling reactions. The trityl group provides exceptional stability and orthogonal protection, enabling selective deprotection and functionalization in complex molecule synthesis. Its compatibility with standard Suzuki-Miyaura conditions and ease of purification make it ideal for constructing bioactive heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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: