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Structure of 1314138-13-0
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This boronate-functionalized pyrrolopyrazole integrates readily into Suzuki-Miyaura coupling reactions under standard conditions. The tetramethylborolane moiety ensures high stability and compatibility with diverse reaction environments, enabling efficient C–C bond formation in complex molecular architectures.
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. Its stable dioxaborolane group enables efficient C–C bond formation under mild conditions, while the dihydropyrrolopyrazole core provides a rigid, nitrogen-rich heterocyclic scaffold relevant to medicinal chemistry and functional materials. The compound exhibits excellent bench stability, minimal air sensitivity, and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular architectures.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: