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Structure of 864754-21-2
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This pyrazole-functionalized boronate ester integrates a tetramethyl-1,3,2-dioxaborolane moiety with a 3-pyridylmethyl scaffold, enabling efficient Suzuki-Miyaura coupling under mild conditions. The sterically protected boronate group ensures high stability and compatibility with diverse reaction environments.
3-[[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]methyl]pyridine serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. Its pyrazole-pyridine scaffold enables efficient construction of biaryl and heteroaryl architectures with excellent functional group tolerance. The stable boronate ester facilitates straightforward purification and bench handling, making it ideal for modular synthesis in medicinal chemistry and materials science applications.
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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: