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Structure of 1034924-06-5
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized pyrimidine derivatives with high efficiency. The methyl substituent enhances solubility and stability, while the electron-deficient heterocycle ensures predictable reactivity.
(2-Methylpyrimidin-5-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its pyrimidine core provides enhanced stability and solubility compared to simpler heterocycles, while the boronic acid functionality facilitates reliable coupling with aryl, vinyl, and heteroaryl halides. The methyl substituent enhances electronic modulation and improves bench stability, making it well-suited for medicinal chemistry and process development workflows.
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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: