16939-18-7

Basic information

• Product Name: Ethanone, diphenylthioxo-
• CAS NO: 16939-18-7
• Molecular Formula: C14H10OS
• Molecular Weight: 226.299
• Mol File: 16939-18-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, diphenylthioxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, diphenylthioxo-(16939-18-7)
• EPA Substance Registry System: Ethanone, diphenylthioxo-(16939-18-7)

Safety Data

• Hazardous Substances Data: 16939-18-7(Hazardous Substances Data)

Upstream product

• 64801-82-7 tetraphenyl-[1,3]oxathiole 
• 92844-65-0 sodium desyl thiosulfate 
• 74950-05-3 2.4-Dibenzoyl-2.4-diphenyl-1.3-dithietan 
• 603-35-0 triphenylphosphine 
• 63369-91-5 α-chloro-α-(chlorosulfenyl)benzyl phenyl ketone 

Downstream Products

• 1273585-27-5 (Z)-2-(4-bromophenylimino)-4,5-diphenyl-1,3-oxathiole 
• 1273585-25-3 (Z)-2-(2,4-dichlorophenylimino)-4,5-diphenyl-1,3-oxathiole 
• 1273585-35-5 (Z)-α-benzoyloxy-β-benzoylthiostilbene 
• 1273585-11-7 (Z)-α-(4-chlorobenzoyloxy)-β-(4-chlorobenzoylthio)stilbene 
• 1273585-28-6 (Z)-2-(4-cyanophenylimino)-4,5-diphenyl-1,3-oxathiole 
• 1273585-23-1 (Z)-2-(phenylimino)-4,5-diphenyl-1,3-oxathiole 
• 1273585-26-4 (Z)-2-(2,6-dichlorophenylimino)-4,5-diphenyl-1,3-oxathiole 
• 1273585-24-2 (Z)-N-(4-chlorophenyl)-4,5-diphenyl-1,3-oxathiol-2-imine 
• 64801-82-7 tetraphenyl-[1,3]oxathiole 
• 92844-64-9 5,6-dibromo-3-phenyl-3-(phenylcarbonyl)-2-thiabicyclo<2.2.1>heptane 
• 7510-34-1 (Z)-1,2,3,4-tetraphenyl-2-butene-1,4-dione 
• 134-81-6 benzil 
• 74950-05-3 2.4-Dibenzoyl-2.4-diphenyl-1.3-dithietan 

Relevant articles and documents

Electrogeneration of (Z)-α-aroyloxy-β-aroylthiostilbenes and (Z)-4,5-diaryl-2-arylimino-1,3-oxathioles by cathodic reduction of monothiobenzils in the presence of electrophilic reagents. Computational B3LYP and RI-MP2 study on the relative stability of ox

Electrochemical reductions of monothiobenzils in the presence of either aroyl or carbonimidoyl dichlorides were carried out, yielding products with sulfur retention. Electrolyses in the presence of aroyl chlorides led to previously unknown (Z)-α-aroyloxy-

Organic Sulfur Compounds, XLVII Dimerization of Monothiobenzil to a 1,3-Dithietane and its Cycloreversion

The thermal dimerization of monothiobenzil (1c) to a 1,3-dithietane (2c) and the photochemical cycloreversion of this heterocycle to 1c is described. - Keywords: Heterocycles, Organic Sulfur Compounds, α-Oxothiones, 1,3-Dithietanes, 1,3-Oxathiols, Photore