1443441-65-3

Basic information

• Product Name: 3-methyl-2-phenyl-5-(p-tolyl)furan
• Synonyms: 3-methyl-2-phenyl-5-(p-tolyl)furan
• CAS NO: 1443441-65-3
• Molecular Weight: 248.324
• Mol File: 1443441-65-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-methyl-2-phenyl-5-(p-tolyl)furan(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methyl-2-phenyl-5-(p-tolyl)furan(1443441-65-3)
• EPA Substance Registry System: 3-methyl-2-phenyl-5-(p-tolyl)furan(1443441-65-3)

Safety Data

• Hazardous Substances Data: 1443441-65-3(Hazardous Substances Data)

Upstream product

• 622-97-9 1-ethenyl-4-methylbenzene 
• 6084-17-9 2-chloro-1-phenylpropan-1-one 
• 7559-36-6 4-methyl-β-nitrostyrene 
• 93-55-0 1-phenyl-propan-1-one 
• 1866-39-3 4-methylcinnamic 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).

Copper-catalyzed regioselective synthesis of furan via tandem cycloaddition of ketone with an unsaturated carboxylic acid under air

A catalytic decarboxylative annulation has been developed for the regioselective synthesis of trisubstituted furans by the cycloaddition of ketones with α,β-unsaturated carboxylic acids under ambient air. A library of furan derivatives were obtained in good yields from the readily available substrates in the combination of a catalytic amount of Cu-salt and a stoichiometric amount of water. Water plays a crucial role in this catalytic transformation. This journal is

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.