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Structure of 947533-31-5
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This boronate moiety integrates a tert-butyl carbamate-protected pyrazole core with two methyl groups at the 3 and 5 positions, delivering enhanced stability and solubility. The electron-rich pyrazole ring facilitates efficient Suzuki-Miyaura coupling under standard conditions, enabling rapid access to functionalized heterocycles in complex molecule synthesis.
(1-(tert-Butoxycarbonyl)-3,5-dimethyl-1H-pyrazol-4-yl)boronic acid serves as a stable, bench-ready building block for palladium-catalyzed cross-coupling reactions. Its pyrazole core, protected with a tert-butyl carbamate group, enables orthogonal functionalization and facilitates purification. The boronic acid moiety reacts efficiently with aryl halides and triflates under standard Suzuki-Miyaura conditions, offering reliable access to substituted pyrazole scaffolds commonly found in medicinal chemistry and agrochemical research.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: