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Structure of 1201657-32-0
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Ethyl 2-methyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)propanoate features a sterically shielded boronate ester paired with a pyrazole heterocycle, enabling reliable coupling in Suzuki-Miyaura reactions. This bench-stable reagent integrates seamlessly into complex molecule assembly workflows.
Ethyl 2-methyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)propanoate serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. The pyrazole moiety enables efficient functionalization in Suzuki-Miyaura coupling, while the sterically hindered tetramethylboronate group ensures high stability and compatibility with diverse reaction conditions. This reagent facilitates rapid access to substituted pyrazole scaffolds commonly found in medicinal chemistry and agrochemical research.
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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: