1398400-07-1

Basic information

• Product Name: (+)-(S)-(E)-3-(4-phenylbut-3-en-2-yl)furan-2(5H)-one
• Synonyms: (+)-(S)-(E)-3-(4-phenylbut-3-en-2-yl)furan-2(5H)-one
• CAS NO: 1398400-07-1
• Molecular Weight: 214.264
• Mol File: 1398400-07-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (+)-(S)-(E)-3-(4-phenylbut-3-en-2-yl)furan-2(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-(S)-(E)-3-(4-phenylbut-3-en-2-yl)furan-2(5H)-one(1398400-07-1)
• EPA Substance Registry System: (+)-(S)-(E)-3-(4-phenylbut-3-en-2-yl)furan-2(5H)-one(1398400-07-1)

Safety Data

• Hazardous Substances Data: 1398400-07-1(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 1398398-94-1 (S)-3-(but-3-en-2-yl)furan-2(5H)-one 
• 61550-02-5 (furan-2-yloxy)-trimethylsilane 
• 307318-11-2 methyl [(E)-1-methyl-3-phenyl-2-propenyl]carbonate 
• 82045-04-3 (rac)-(E)-2-acetoxy-4-phenylbut-3-ene 

Relevant articles and documents

Iridium-catalyzed regioselective and enantioselective allylation of trimethylsiloxyfuran

We report the regio- and enantioselective allylation of an ester enolate, trimethylsiloxyfuran. This enolate reacts at the 3-position with linear aromatic allylic carbonates or aliphatic allylic benzoates to form the branched substitution products in the presence of a metallacyclic iridium catalyst. This process provides access to synthetically important 3-substituted butenolides in enantioenriched form. Stoichiometric reactions of the allyliridium intermediate suggest that the trimethylsiloxyfuran is activated by the carboxylate leaving group.