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Structure of 1616930-45-0
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Methyl 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-3-carboxylate features a boronate ester group enabling efficient Suzuki-Miyaura coupling. The tetramethyl-substituted dioxaborolane enhances stability and solubility in organic media. This bench-stable reagent integrates readily into complex molecule synthesis, particularly in pharmaceutical and agrochemical scaffold elaboration.
Methyl 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-3-carboxylate serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. The boronic ester functionality enables efficient C–C bond formation under mild conditions, while the pyrazole core provides a versatile heterocyclic scaffold. Its excellent functional group tolerance and ease of purification make it ideal for constructing complex molecular architectures in medicinal chemistry and materials science workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: