39511-12-1

Basic information

• Product Name: 2-Propen-1-one, 3-(2-furanyl)-1-phenyl-, (2E)-
• CAS NO: 39511-12-1
• Molecular Formula: C13H10O2
• Molecular Weight: 198.221
• Mol File: 39511-12-1.mol
• Article Data: 44

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 3-(2-furanyl)-1-phenyl-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 3-(2-furanyl)-1-phenyl-, (2E)-(39511-12-1)
• EPA Substance Registry System: 2-Propen-1-one, 3-(2-furanyl)-1-phenyl-, (2E)-(39511-12-1)

Safety Data

• Hazardous Substances Data: 39511-12-1(Hazardous Substances Data)

Upstream product

• 98-01-1 furfural 
• 98-86-2 acetophenone 
• 70-11-1 α-bromoacetophenone 
• 20689-54-7 (E)-3-(2-furyl)acryloyl chloride 
• 603-33-8 triphenylbismuthane 
• 3282-32-4 2-diazo-acetophenone 
• 98-00-0 (2-furyl)methyl alcohol 
• 6048-29-9 triphenylphenacylphosphonium bromide 
• 3406-03-9 2-(phenylsulfonyl)acetophenone 
• 98-02-2 2-thiolomethyl-furan 
• 110-00-9 furan 
• 3506-36-3 3-dimethylaminopropiophenone 
• 611-73-4 Benzoylformic acid 
• 539-47-9 3-(fur-2-yl)crotonic acid 

Downstream Products

• 59283-36-2 3-[2]furyl-1-phenyl-propylamine 
• 92200-34-5 3-(2'-furyl)-4-nitro-1-phenylbutan-1-one 
• 77607-74-0 4-(furan-2-yl)-2-oxo-6-phenyl-1,2-dihydropyridine-3-carbonitrile 
• 126888-03-7 3-cyano-4-(2'-furyl)-6-phenylpyridinethione 
• 131841-92-4 4-Furan-2-yl-2-methylsulfanyl-6-phenyl-nicotinonitrile 
• 1100793-87-0 (2S,3R,4R,5R)-methyl 4-benzoyl-3-(2-furyl)-5-phenylpyrrolidine-2-carboxylate 
• 1354541-49-3 (3,4-diphenylcyclobutane-1,2-diyl)bis(furan-2-ylmethanone) 

Relevant articles and documents

Novelty of Claisen-Schmidt condensation of biomass-derived furfural with acetophenone over solid super base catalyst

Valorization of biomass into value added chemicals and products using green technologies has been a subject matter of several papers. Claisen-Schmidt condensation of furfural with acetophenone to produce the α,β-unsaturated keto compound, 3-(furan-2-yl)-1

Mechanochemical Syntheses of N-Containing Heterocycles with TosMIC

A mechanochemical van Leusen pyrrole synthesis with a base leads to 3,4-disubstitued pyrroles in moderate to excellent yields. The developed protocol is compatible with a range of electron-withdrawing groups and can also be applied to the synthesis of oxazoles. Attempts to mechanochemically convert the resulting pyrroles into porphyrins proved to be difficult.

Donor-acceptor fluorophores as efficient energy transfer photocatalysts for [2 + 2] photodimerization

Mild [2 + 2] photodimerization of enone substrates was induced by donor-acceptor fluorophores. Enone substrates were activated efficiently for anti-head to head dimerizations with a high yield (up to 83%) and high selectivity. The adjustable excited state potential also allows donor-acceptor fluorophores to be used for isomerization of the above substrates, confirming the potential of donor-acceptor fluorophores as energy transfer photocatalysts.