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Structure of 1083326-46-8
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This boronate-functionalized pyrazole derivative integrates seamlessly into cross-coupling reactions, enabling efficient construction of complex heterocyclic architectures. The tetramethyl-1,3,2-dioxaborolane moiety ensures high stability and compatibility under standard reaction conditions.
2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetamide serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The pyrazole moiety provides a rigid, bioactive heterocyclic scaffold, while the pinacol boronate ester enables stable, air-tolerant handling and broad functional group compatibility. This compound facilitates efficient C–C bond formation under mild conditions, enabling rapid access to complex molecular architectures in medicinal chemistry and materials science applications.
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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: