100910-02-9

Basic information

• Product Name: 3-phenyl-2,5-diethylfuran
• Synonyms: 3-phenyl-2,5-diethylfuran
• CAS NO: 100910-02-9
• Molecular Weight: 200.28
• Mol File: 100910-02-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-phenyl-2,5-diethylfuran(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl-2,5-diethylfuran(100910-02-9)
• EPA Substance Registry System: 3-phenyl-2,5-diethylfuran(100910-02-9)

Safety Data

• Hazardous Substances Data: 100910-02-9(Hazardous Substances Data)

Upstream product

• 100909-99-7 (Z)-1-(3-phenyl-5-ethyl-1,4,2-dioxazol-5-yl)-1-penten-3-one 
• 100910-00-7 1-phenyl-1-(3-phenyl-5-ethyl-1,4,2-dioxazol-5-yl)-3-pentanone 
• 100910-01-8 4-phenyl-3,6-octanedione 
• 10504-06-0 2,5-diethyl-furan 

Relevant articles and documents

Michael Adducts of a Half-Blocked Enedione as Sources of 3-Substituted 2,5-Diketones and 2,5-Dialkylfurans

The dioxazolylbutenones 2a, formed by isomerization of the Diels-Alder adducts of 2,5-dimethylfuran with (nitrosocarbonyl)benzene , are efficient Michael acceptors of a wide variety of carbon and heteroatom nucleophiles.The resulting adducts 5 function as half-blocked 1,4-diones.They can be converted into the corresponding diketones 10 by hot aqueous EtOH or Pd-H2 or into the 3-substituted 2,5-dimethylfurans 19 by BF3, either directly or by way of 10.Hydroperoxide anion adds conjugatively to 2a to give the epoxide 23, but 1,2-addition is competitive and is followed by dioxazole ring opening to give a peroxy compound regarded as 21.The cycloaddition of 2,5-dialkylfurans and nitrosocompounds is general, but 2-methylfuran appears to add (although in poor yield) in the opposite mode, the adduct spontaneously isomerizing to the mono-O-benzoyloximino enedione 32.