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Structure of 1372713-72-8
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This boronate moiety features a methyl-substituted triazole scaffold, delivering enhanced stability and solubility in polar solvents. The electron-deficient triazolyl group facilitates efficient Suzuki-Miyaura coupling under mild conditions, enabling direct functionalization of aryl halides without requiring additional ligands.
(2-Methyl-2H-1,2,3-triazol-4-yl)boronic acid serves as a stable, bench-compatible building block for Suzuki-Miyaura cross-coupling reactions. Its triazolylboronic acid functionality enables efficient C–C bond formation with aryl and heteroaryl halides under mild conditions, offering excellent functional group tolerance and straightforward purification. This reagent functions as a key scaffold in the synthesis of triazole-containing bioactive molecules and advanced heterocyclic systems.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: