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Structure of 6228-47-3
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Catalyst for the carboxylation of styrene oxideReactant involved in:Epoxidation of arylalkenesBoration of allylic epoxidesWittig reactionsSelective dimerization of -olefinsSynthesis of indoles
Triphenyl(propyl)phosphonium bromide serves as a reliable reagent for the Wittig reaction, enabling efficient conversion of aldehydes and ketones into alkenes with high stereoselectivity. Its bench-stable solid form facilitates handling and purification, while the propyl group offers favorable steric and electronic properties for controlled olefination. This reagent functions effectively in standard organic synthesis workflows, particularly in the construction of conjugated systems and complex molecular architectures.
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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-H335
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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: