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Structure of 50670-51-4
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4'-(Bromomethyl)-[1,1'-biphenyl]-4-carbonitrile features a bromomethyl group flanked by a biphenyl scaffold and a terminal nitrile, enabling direct functionalization in cross-coupling and conjugation workflows. The electron-deficient aryl bromide site facilitates palladium-catalyzed transformations, while the nitrile moiety provides polarity and synthetic handle for downstream derivatization. This compound serves as a modular building block in pharmaceutical and materials synthesis.
4'-(Bromomethyl)-[1,1'-biphenyl]-4-carbonitrile serves as a versatile bifunctional building block for transition-metal-catalyzed cross-coupling reactions. The bromomethyl group enables efficient Suzuki-Miyaura and Negishi couplings, while the para-cyano group provides orthogonal reactivity and enhanced solubility. This stable, bench-ready reagent facilitates rapid access to functionalized biphenyl scaffolds commonly found in pharmaceutical intermediates and advanced materials.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H290-H314-H318
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: