201216-01-5

Basic information

• Product Name: phenyl(2-(phenylsulfonyl)phenyl)methanone
• Synonyms: phenyl(2-(phenylsulfonyl)phenyl)methanone
• CAS NO: 201216-01-5
• Molecular Weight: 322.384
• Mol File: 201216-01-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: phenyl(2-(phenylsulfonyl)phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl(2-(phenylsulfonyl)phenyl)methanone(201216-01-5)
• EPA Substance Registry System: phenyl(2-(phenylsulfonyl)phenyl)methanone(201216-01-5)

Safety Data

• Hazardous Substances Data: 201216-01-5(Hazardous Substances Data)

Upstream product

• 71-43-2 benzene 
• 5162-03-8 (2-chlorophenyl)(phenyl)methanone 
• 873-55-2 sodium benzenesulfonate 
• 4661-46-5 2-carboxybenzene diazonium chloride 
• 58844-73-8 2-(phenylsulfonyl)benzoic acid 
• 1527-12-4 2-(phenylthio)benzoic acid 
• 13963-35-4 2-(phenylthio)toluene 
• 17333-74-3 2-methylbenzene diazonium 
• 7446-70-0 aluminium trichloride 
• 34684-21-4 2-chlorosulfonylbenzoyl chloride 
• 62574-72-5 3,3-dichloro-3H-benz[c][1,2]oxathiol 1,1-dioxide 
• 127-63-9 diphenyl sulphone 
• 100-52-7 benzaldehyde 

Downstream Products

• 24237-73-8 2-Benzhydryl-benzenesulfinic acid 
• 24237-76-1 (2-Benzenesulfonyl-phenyl)-phenyl-acetic acid methyl ester 
• 24237-75-0 2-Benzhydryl-benzenesulfonyl chloride 
• 24237-72-7 1-Benzenesulfonyl-2-benzyl-benzene 
• 127-63-9 diphenyl sulphone 
• 65-85-0 benzoic acid 
• 24237-71-6 (2-Benzenesulfonyl-phenyl)-phenyl-methanol 
• 19103-71-0 (2-benzenesulfonyl-phenyl)-diphenyl-methanol 

Relevant articles and documents

Hantzsch Ester as a Visible-Light Photoredox Catalyst for Transition-Metal-Free Coupling of Arylhalides and Arylsulfinates

Diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate (HEH) has been utilized as a visible-light photoredox catalyst for the cross coupling of arylhalides and arylsulfinates without transition metal, sacrificial agent, and mediator. This method is compatible with various functional groups and provides diaryl sulfones in good to high yields. Mechanistic studies indicate that this reaction undergoes the stepwise light irradiation of HE?, single electron transfer (SET) in donor–acceptor complex (DAC) from *HE? to arylhalide, trapping of aryl radical with sulfinate, and SET oxidation of sulfone radical anion by HE. to sulfone by the DAC method.