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Structure of 1200537-40-1
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This pyrazole derivative features a methoxyethyl substituent and a sterically shielded tetramethylborolane group, enabling efficient Suzuki-Miyaura coupling under standard conditions. The electron-rich core enhances reactivity while maintaining bench stability and moisture tolerance, simplifying handling in synthetic workflows.
1-(2-Methoxyethyl)-3,5-dimethyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate group enables efficient C–C bond formation under mild conditions, while the 2-methoxyethyl and dimethyl substituents provide enhanced solubility and functional group tolerance. This pyrazole scaffold is well-suited for constructing diverse heterocyclic frameworks 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-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: