1326304-63-5

Basic information

• Product Name: 5-(4-fluorophenyl)-3-methylfuran-2(5H)-one
• Synonyms: 5-(4-fluorophenyl)-3-methylfuran-2(5H)-one
• CAS NO: 1326304-63-5
• Molecular Weight: 192.19
• Mol File: 1326304-63-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5-(4-fluorophenyl)-3-methylfuran-2(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-fluorophenyl)-3-methylfuran-2(5H)-one(1326304-63-5)
• EPA Substance Registry System: 5-(4-fluorophenyl)-3-methylfuran-2(5H)-one(1326304-63-5)

Safety Data

• Hazardous Substances Data: 1326304-63-5(Hazardous Substances Data)

Upstream product

• 22122-36-7 3-methyl-5H-furan-2-one 
• 176041-42-2 triisopropyl((3-methylfuran-2-yl)oxy)silane 
• 1765-93-1 4-fluoroboronic acid 
• 616-02-4 citraconic acid anhydride 

Downstream Products

• 1326304-52-2 phenyl (R)-5-(4-fluorophenyl)-3-methyl-2-oxo-2,3-dihydrofuran-3-carboxylate 
• 1326304-54-4 2,2,2-trichloroethyl 2-(4-fluorophenyl)-4-methyl-5-oxo-2,5 dihydrofuran-2-carboxylate 
• 1326304-53-3 2,2,2-trichloroethyl (R)-5-(4-fluorophenyl)-3-methyl-2-oxo-2,3-dihydrofuran-3-carboxylate 
• 1326304-40-8 5-(4-fluorophenyl)-3-methylfuran-2-yl phenyl carbonate 
• 1326304-41-9 5-(4-fluorophenyl)-3-methylfuran-2-yl 2,2,2-trichloroethyl carbonate 

Relevant articles and documents

Comparative studies of palladium and copper-catalysed γ-arylation of silyloxy furans with diaryliodonium salts

The γ-arylation of substituted silyl-activated butenolides has been studied using a broad scope of unsymmetrical hypervalent diaryliodonium salts via a palladium- or copper-catalysed coupling reaction, yielding interesting reactivity trends. The mild catalytic conditions and coupling partner variability provide access to synthetically useful building blocks toward the pursuit of aryl-lactone containing natural products and allows for facile diversification.