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Structure of 2739830-29-4
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This boronate moiety features a cyano-substituted pyrazole scaffold, delivering enhanced stability and compatibility in cross-coupling reactions. The methyl group at the 1-position improves solubility, while the electron-deficient pyrazole ring enables efficient palladium-catalyzed transformations under standard conditions.
(3-Cyano-1-methyl-1H-pyrazol-5-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The cyano group enhances electrophilicity for downstream functionalization, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction conditions. Its orthogonality to common protecting groups and reliable performance in late-stage diversification make it a practical choice for medicinal chemistry and materials synthesis 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: