151414-77-6

Basic information

• Product Name: o-(Prop-2-enyloxy)phenyllead Triacetate
• Synonyms: o-(Prop-2-enyloxy)phenyllead Triacetate
• CAS NO: 151414-77-6
• Molecular Weight: 517.504
• Mol File: 151414-77-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: o-(Prop-2-enyloxy)phenyllead Triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: o-(Prop-2-enyloxy)phenyllead Triacetate(151414-77-6)
• EPA Substance Registry System: o-(Prop-2-enyloxy)phenyllead Triacetate(151414-77-6)

Safety Data

• Hazardous Substances Data: 151414-77-6(Hazardous Substances Data)

Upstream product

• 1600-27-7 mercury(II) diacetate 
• 546-67-8 lead(IV) tetraacetate 
• 151414-76-5 o-(prop-2-enyloxy)phenylboronic acid 

Downstream Products

• 151452-01-6 alpha-methylphenylacyl-{o-(prop-2-enyloxy)phenyl}-lead diacetate 
• 93-55-0 1-phenyl-propan-1-one 
• 24892-63-5 1-allyloxy-2-iodobenzene 
• 10101-63-0 lead(II) iodide 
• 55000-07-2 o-(prop-2-enyloxy)phenyl azide 
• 19347-08-1 acetic acid 1-methyl-2-oxo-2-phenyl-ethyl ester 

Relevant articles and documents

Mechanism of Arylation of Nucleophiles by Aryllead Triacetates. Part 1. Exclusion of a Pathway involving Aryl Free Radicals

o-(Prop-2-enyloxy)phenyllead triacetate 6, which was obtained by treatment of the corresponding boronic acid with lead tetraacetate, has been shown to react with iodide and azide ions, 2,4,6-trimethylphenol, ethyl 2-oxocyclopentanecarboxylate, and the sodium salt of 2-nitropropane to give only those products which, in a formal sense, are derived by direct nucleophilic displacement of the Pb(OAc)3 group.The complete absence of 3-substituted dihydrobenzofurans among the products is strong evidence that aryl free radicals are not involved in the arylation reactions of aryllead triacetates.