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Structure of 911210-49-6
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This boronate reagent features a cyano-substituted aryl ring paired with a methyl group at the ortho position, delivering enhanced stability and predictable reactivity in Suzuki-Miyaura cross-coupling. The electron-withdrawing nitrile group modulates electronic density, enabling efficient coupling under mild conditions. Bench-stable and moisture-tolerant, it integrates seamlessly into synthetic workflows requiring precise functionalization of biaryl scaffolds.
(3-Cyano-4-methylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ortho-cyano and methyl substituents provide enhanced stability and tunable electronic properties, facilitating downstream functionalization. The boronic acid moiety exhibits excellent bench stability, ease of purification, and compatibility with diverse reaction partners, making it well-suited for the synthesis of substituted biaryls and complex heterocyclic scaffolds in medicinal chemistry and materials science.
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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
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Precautionary Statements : P264-P270-P301+P310-P330-P501
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Lot numbers can be found on the outside label of a product: