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Structure of 1218790-73-8
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This boronate moiety integrates a methoxymethyl-protected pyrazole scaffold with a trifluoromethyl group, delivering enhanced stability and solubility under standard conditions. The electron-deficient arylboronic acid facilitates efficient Suzuki-Miyaura coupling reactions in complex molecule synthesis.
(1-(Methoxymethyl)-3-(trifluoromethyl)-1H-pyrazol-4-yl)boronic acid serves as a versatile building block for Suzuki-Miyaura couplings, enabling efficient construction of biaryl and heteroaryl scaffolds. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the methoxymethyl substituent provides orthogonal protection and improved solubility. Bench-stable and readily purified by flash chromatography, it functions reliably in diverse reaction conditions, facilitating access to functionalized pyrazole derivatives relevant to medicinal chemistry and agrochemical development.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: