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Structure of 3607-17-8
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Reactant involved in:Synthesis of functionalized polyurethanes using cationic ring-opening polymerization and click chemistrySemipinacol rearrangement and direct arylationOlefination of benzaldehydesC-H activation / cycloisomerizationIntramolecular dehydrobrominationCycloisomerizations of bromodienes and enynes
(3-Bromopropyl)triphenylphosphonium bromide serves as a versatile alkylating agent in nucleophilic substitution reactions, enabling efficient synthesis of phosphonium salts and facilitating Wittig-type olefination precursors. Its bench-stable solid form and high functional group tolerance make it well-suited for iterative C–C bond formation and heterocycle construction in medicinal chemistry workflows.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: