4746-79-6

Basic information

• Product Name: 1-(2'-benzoylphenyl)-2-phenylethane-1,2-dione
• Synonyms: 1-(2'-benzoylphenyl)-2-phenylethane-1,2-dione
• CAS NO: 4746-79-6
• Molecular Weight: 314.34
• Mol File: 4746-79-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(2'-benzoylphenyl)-2-phenylethane-1,2-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2'-benzoylphenyl)-2-phenylethane-1,2-dione(4746-79-6)
• EPA Substance Registry System: 1-(2'-benzoylphenyl)-2-phenylethane-1,2-dione(4746-79-6)

Safety Data

• Hazardous Substances Data: 4746-79-6(Hazardous Substances Data)

Upstream product

• 53133-97-4 1.2c-dihydroxy-1r.2t-diphenyl-indanone-⁽³⁾ 
• 546-67-8 lead(IV) tetraacetate 
• 71-43-2 benzene 
• 5324-00-5 2,3-diphenyl-1H-indene 
• 64-19-7 acetic acid 
• 67-64-1 acetone 
• 221458-86-2 (phenyl)[2-(2-phenylethynyl)phenyl]methanone 
• 24423-97-0 1,2,3-triphenyl-1-propene 
• 91859-82-4 1,4-Diphenyl-4,5-dihydro-1H-1,4-epoxido-benzo[d][1,2]dioxepin 
• 1801-42-9 2,3-diphenyl-1H-inden-1-one 
• 171969-52-1 1,3-Diphenyl-isochroman 
• 62423-27-2 phenyl-(3-phenyl-isobenzofuran-1-yl)-ketone 
• 53067-91-7 2-(2-benzoylphenyl)-1-phenylethan-1-one 
• 18636-54-9 1,2-diphenyl-1H-indene 

Downstream Products

• 5398-11-8 3-phenylphthalide 
• 60079-98-3 10-phenyl-9-anthracene-ol 
• 39127-30-5 2-butyl-3-phenylisoindolin-1-one 
• 1726-15-4 3-phenyl-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-one 
• 85-52-9 2-Benzoylbenzoic acid 
• 65-85-0 benzoic acid 
• 5471-63-6 1,3-diphenylisobenzofuran 

Relevant articles and documents

Method for preparing 1,2-dicarbonyl compound by photocatalytic oxidation reaction

The invention discloses a method for preparing a 1,2-dicarbonyl compound by a photocatalytic oxidation reaction. The method includes the following steps: mixing an unsaturated triple bond compound, acoordination catalyst and a solvent to obtain a solution

Reaction of 1,2,4,5-Tetroxan with Antimony Pentachloride or Liquid Sulphur Dioxide: Heterolytic Fission of Carbon-Oxygen or Oxygen-Oxygen Bonds

The reactions of 11 kinds of tetroxans with antimony pentachloride have been investigated.A mixture of ketone (aldehyde) and ester (carboxylic acid) was obtained, the ratio of which was found to depend on the substituents.In the presence of the catalyst cis-3,6-bis(3-benzoylpropyl)-1,2,4,5-tetroxan rearranges to the trans-isomer.In the reaction of some tetroxans with liquid sulphur dioxide, a mixture of ester and ketone was obtained in a molar ratio of 1:1.Reductive ozonolysis of some alkenes in the presence of 10 mol equiv. of sulphur dioxide in methylene chloride gave the corresponding carbonyl compounds in good yields.