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Structure of 1375301-91-9
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This boronate ester features a cyclopropyl-substituted pyrimidine core, enabling efficient cross-coupling under standard conditions. The tetramethyl-dioxaborolane moiety enhances stability and reactivity, while the cyclopropyl group imparts favorable steric and electronic properties for C–C bond formation in medicinal chemistry and materials synthesis.
2-Cyclopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine serves as a versatile Suzuki-Miyaura coupling partner, enabling efficient C–C bond formation under mild conditions. The boronate ester group exhibits excellent stability, tolerance to diverse functional groups, and compatibility with common reaction protocols. Its pyrimidine core provides a robust scaffold for constructing biologically relevant heterocycles and pharmaceutical intermediates.
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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: