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Structure of 185626-73-7
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(3-Bromophenyl)triphenylsilane features a brominated phenyl group attached to a triphenylsilane core, delivering a stable, bench-ready arylsilane reagent. The ortho-bromine facilitates palladium-catalyzed cross-coupling reactions, while the bulky silane moiety enhances solubility and prevents protodesilylation. This combination enables efficient C–C bond formation in complex molecule synthesis.
(3-Bromophenyl)triphenylsilane serves as a stable, bench-ready arylsilane building block for palladium-catalyzed cross-coupling reactions. Its bromo-substituted phenyl group enables efficient Suzuki-Miyaura and Negishi couplings, while the triphenylsilyl moiety provides excellent functional group tolerance and ease of purification. This reagent facilitates the construction of biaryl scaffolds common in pharmaceutical and materials chemistry.
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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 : H315-H319
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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: