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Structure of 936250-17-8
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This boronate-functional pyrimidine integrates seamlessly into Suzuki-Miyaura cross-coupling reactions under standard conditions. The dimethoxy substituents enhance solubility and stability, while the tetramethyl-dioxaborolane group enables efficient palladium-catalyzed bond formation. Designed for synthetic efficiency in complex molecule assembly.
2,4-Dimethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pyrimidine core provides a stable heterocyclic scaffold with predictable reactivity, while the tetramethylboronate group enables efficient coupling under mild conditions. Its bench-stable nature and tolerance to diverse functional groups facilitate reliable synthesis of complex molecular architectures in medicinal chemistry and materials science workflows.
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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: