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Structure of 1346245-52-0
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N-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-acetamide features a boronate ester group flanked by sterically protected tetramethylcyclohexadienyl moieties, enabling robust coupling under mild conditions. This bench-stable reagent integrates efficiently into Suzuki-Miyaura cross-coupling workflows, delivering pyrazole-based scaffolds with high functional group tolerance.
N-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-acetamide serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate moiety enables reliable coupling with aryl and heteroaryl halides under mild conditions, while the pyrazole-acetamide core offers stability and compatibility with diverse functional groups. Its bench-stable nature and ease of purification facilitate efficient synthesis of complex 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: