108164-59-6

Basic information

• Product Name: 2,2-bis(phenylthio)-4-phenyl-butane
• Synonyms: 2,2-bis(phenylthio)-4-phenyl-butane
• CAS NO: 108164-59-6
• Molecular Weight: 350.549
• Mol File: 108164-59-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,2-bis(phenylthio)-4-phenyl-butane(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-bis(phenylthio)-4-phenyl-butane(108164-59-6)
• EPA Substance Registry System: 2,2-bis(phenylthio)-4-phenyl-butane(108164-59-6)

Safety Data

• Hazardous Substances Data: 108164-59-6(Hazardous Substances Data)

Upstream product

• 2550-26-7 4-Phenyl-2-butanone 
• 20137-71-7 2-methyl-2-(2-phenylethyl)-1,3-dithiane 
• 16520-62-0 4-Phenyl-1-butyne 
• 108-98-5 thiophenol 

Downstream Products

• 2550-26-7 4-Phenyl-2-butanone 
• 39854-49-4 2-methyl-2-(2-phenylethyl)-1,3-dithiane 
• 20137-71-7 2-methyl-2-(2-phenylethyl)-1,3-dithiane 

Relevant articles and documents

Hydrothiolation of unactivated alkynes catalyzed by indium(III) bromide

Indium(III) bromide is found to catalyze efficiently the hydrothiolation of unactivated alkynes with various thiols under mild conditions to produce the corresponding dithioacetals in excellent yields. However, addition of aromatic thiols on aromatic alky

ELECTROREDUCTIVE CLEAVAGE OF CARBON-SULPHUR BONDS IN DITHIOACETALS

The carbon-sulphur bond in aliphatic diphenyldithioacetals, α-carbonyldiphenyldithioacetals and α-carbonylketene dimethyldithioacetals can be cleaved cathodically on mercury (Hg) or glassy carbon (GC) electrodes.In the presence of tetrabutylammoniumhydrog