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Structure of 942922-07-8
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This pyrimidine derivative features a 4-methylpiperazine moiety paired with a boronate ester group, enabling efficient Suzuki-Miyaura cross-coupling under standard conditions. The tetramethyl-substituted dioxaborolane enhances stability and reactivity, while the electron-rich piperazine facilitates functionalization in late-stage diversification. Designed for streamlined synthesis in medicinal chemistry and materials science.
2-(4-Methylpiperazin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The pyrimidine core provides a rigid, electron-deficient scaffold compatible with diverse nucleophiles, while the pinacol boronate ester ensures excellent stability and ease of handling. This compound facilitates efficient C–C bond formation under mild conditions, enabling rapid access to functionalized heterocyclic architectures relevant in medicinal chemistry and materials science.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: