32120-82-4

Basic information

• Product Name: Ethanone, 2,2'-sulfinylbis[1-phenyl-
• CAS NO: 32120-82-4
• Molecular Formula: C16H14O3S
• Molecular Weight: 286.351
• Mol File: 32120-82-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethanone, 2,2'-sulfinylbis[1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2,2'-sulfinylbis[1-phenyl-(32120-82-4)
• EPA Substance Registry System: Ethanone, 2,2'-sulfinylbis[1-phenyl-(32120-82-4)

Safety Data

• Hazardous Substances Data: 32120-82-4(Hazardous Substances Data)

Upstream product

• 93-89-0 benzoic acid ethyl ester 
• 2813-22-1 2-methanesulfinyl-1-phenyl-ethanone 
• 2461-80-5 diphenacyl sulfide 
• 94-36-0 dibenzoyl peroxide 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 1252670-61-3 C₅₆H₉₈N₄O₁₉SSi₄ 
• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 
• 94-41-7 benzalacetophenone 
• 956-04-7 3-(4-chlorophenyl)-1-phenylprop-2-en-1-one 
• 4224-87-7 4-methyl-chalcone 

Relevant articles and documents

The studies of enhanced fluorescence in the two novel ternary rare-earth complex systems

Two novel ternary rare-earth complexes SmL5?L? (ClO4)2?7H2O and EuL5? L'? (ClO4)2?6H2O (the first ligand L = C6H5 COCH2SOCH

Stereoselective synthesis of cis-2,6-disubstituted morpholines and 1,4-oxathianes by intramolecular reductive etherification of 1,5-diketones

A simple and efficient, Lewis acid catalysed reductive etherification strategy for the stereoselective synthesis of cis-2,6- disubstituted morpholines and 1,4-oxathianes starting from readily available 1,5-diketones has been developed. The strategy is used in the total synthesis of morpholine-based natural products (±)-chelonin A and formal total synthesis of (±)-chelonin C.

Reaction of the α,α'-dianion of β-ketosulfoxide

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