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Structure of 847818-71-7
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This pyrazole derivative features a methoxyethyl substituent and a boronate ester group, enabling efficient Suzuki-Miyaura coupling under standard conditions. The tetramethyl-1,3,2-dioxaborolane moiety ensures stability and compatibility with aqueous and protic solvents, while the electron-rich pyrazole core supports diverse functionalization in medicinal chemistry and materials synthesis.
1-(2-Methoxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pyrazole core provides metabolic stability and hydrogen-bonding capacity, while the 2-methoxyethyl side chain enhances solubility and modulates polarity. The tetramethyl-substituted dioxaborolane moiety ensures excellent bench stability, low toxicity, and high functional group tolerance, enabling efficient coupling under mild conditions. This reagent facilitates rapid assembly 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: