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Structure of 864754-17-6
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This pyrazole derivative features a boronate ester group enabling efficient Suzuki-Miyaura coupling, paired with a dioxolane-protected aldehyde handle. The tetramethyl-substituted boronate moiety ensures stability and compatibility under standard reaction conditions.
1-(1,3-Dioxolan-2-ylmethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole serves as a versatile boron-containing building block for Suzuki-Miyaura coupling reactions. The pyrazole core provides a stable heterocyclic scaffold with tunable nitrogen functionality, while the 1,3-dioxolane-2-ylmethyl group offers protection for aldehyde intermediates. The pinacol boronate moiety enables efficient cross-coupling under mild conditions, with excellent stability and ease of purification, making it ideal for iterative synthesis 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: