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Structure of 5421-53-4
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Bis(4-(tert-butyl)phenyl)iodonium chloride delivers high electrophilic reactivity in C–H functionalization and arylation processes. The sterically shielded aryl groups enhance stability and solubility, enabling efficient transfer of aryl fragments under mild conditions. This bench-stable reagent simplifies access to complex aromatic architectures in synthetic workflows.
Bis(4-(tert-butyl)phenyl)iodonium chloride serves as a stable, bench-ready arylating agent enabling efficient C–C and C–heteroatom bond formation under mild conditions. Its sterically hindered aryl groups enhance solubility and reduce side reactions, while the iodonium moiety facilitates selective transfer of 4-(tert-butyl)phenyl groups in cross-coupling and electrophilic functionalization processes. Ideal for late-stage modification and heterocycle synthesis due to excellent functional group tolerance and ease of purification.
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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 : P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362+P364
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Lot numbers can be found on the outside label of a product: