1443441-68-6

Basic information

• Product Name: 5-(4-fluorophenyl)-3-methyl-2-phenylfuran
• Synonyms: 5-(4-fluorophenyl)-3-methyl-2-phenylfuran
• CAS NO: 1443441-68-6
• Molecular Weight: 252.288
• Mol File: 1443441-68-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-(4-fluorophenyl)-3-methyl-2-phenylfuran(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-fluorophenyl)-3-methyl-2-phenylfuran(1443441-68-6)
• EPA Substance Registry System: 5-(4-fluorophenyl)-3-methyl-2-phenylfuran(1443441-68-6)

Safety Data

• Hazardous Substances Data: 1443441-68-6(Hazardous Substances Data)

Upstream product

• 405-99-2 para-fluorostyrene 
• 6084-17-9 2-chloro-1-phenylpropan-1-one 
• 5153-69-5 4-fluoro-β-nitrostyrene 
• 93-55-0 1-phenyl-propan-1-one 
• 459-32-5 4-fluorocinnamic acid 

Relevant articles and documents

A co-operative effect of visible light photo-catalysis and CoFe2O4 nanoparticles for green synthesis of furans in water

A novel approach to poly-functionalized furan synthesis is disclosed via oxidative decarboxylative [3+2] cycloaddition using co-operative catalysis by visible light and CoFe2O4 nanoparticles under ambient reaction conditions with water as a solvent. Although the reported method is efficient without catalyst in the presence of visible light (70% yield in 4 h at rt), the use of catalyst not only increases the yield (91%) but also accelerates the conversion rate (2 h at rt).

Regioselective Synthesis of Multisubstituted Furans via Copper-Mediated Coupling between Ketones and β-Nitrostyrenes

A copper-mediated intermolecular annulation of alkyl ketones and β-nitrostyrenes has been developed for the regioselective synthesis of multisubstituted furan derivatives in good yields. This protocol is applicable to both cyclic and acyclic ketones. (Che

Synthesis of polysubstituted furans via copper-mediated annulation of alkyl ketones with α,β-unsaturated carboxylic acids

A novel copper-mediated annulation of alkyl ketones with α,β-unsaturated carboxylic acids has been accomplished. This reaction provides a facile and regio-defined method for the synthesis of 2,3,5-trisubstituted furans from simple chemical reagents.