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Structure of 1308298-23-8
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This boronate moiety features a trifluoromethylpyrimidine scaffold, delivering enhanced metabolic stability and electron-deficient character. It integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, enabling efficient access to functionalized heteroaryl architectures in medicinal chemistry and materials science.
(2-(Trifluoromethyl)pyrimidin-5-yl)boronic acid serves as a versatile building block in cross-coupling reactions, enabling efficient construction of biologically relevant pyrimidine derivatives. Its trifluoromethyl group enhances metabolic stability and modulates electronic properties, while the boronic acid functionality facilitates reliable Suzuki-Miyaura coupling under standard conditions. The compound exhibits excellent bench stability, ease of handling, and compatibility with diverse functional groups, making it ideal 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: