13133-62-5

Basic information

• Product Name: thiophenolate
• Synonyms: thiophenolate
• CAS NO: 13133-62-5
• Molecular Weight: 109.172
• Mol File: 13133-62-5.mol
• Article Data: 28

Chemical Properties

• CAS DataBase Reference: thiophenolate(CAS DataBase Reference)
• NIST Chemistry Reference: thiophenolate(13133-62-5)
• EPA Substance Registry System: thiophenolate(13133-62-5)

Safety Data

• Hazardous Substances Data: 13133-62-5(Hazardous Substances Data)

Upstream product

• 831-91-4 Benzyl phenyl sulfide 
• 100-47-0 cyanobenzene 
• 218-01-9 chrysene radical anion 
• 129-00-0 pyrene anion radical 
• 92-94-4 p-terphenyl radical anion 
• 34518-98-4 phenanthridine radical ion 
• 72490-91-6 benzoquinoline radical ion 
• 72490-90-5 benzoquinoline radical ion 
• 63707-12-0 1-(4-methylphenylsulfanyl)-2-phenylethyne 
• 61642-86-2 S-phenyl thiocarbamate 
• 79108-34-2 thiophenyl fluorene-9-carboxylate 
• 591-50-4 iodobenzene 
• 75-66-1 2-methylpropan-2-thiol 
• 108-98-5 thiophenol 

Downstream Products

• 64672-74-8 C₂₆H₂₄S₄ 
• 31238-57-0 diphenyl(phenylthiomethyl)phosphine oxide 
• 28856-77-1 3-phenylthiopyridine 
• 3019-20-3 isopropylthiobenzene 
• 22190-12-1 2-phenylsulfanyl-quinoline 
• 102690-35-7 2-phenylmercapto-3,3-dimethylbutanal 
• 139-66-2 diphenyl sulfide 
• 3459-94-7 1,4-bis(phenylthio)benzene 
• 13343-26-5 phenyl p-chlorophenyl sulfide 
• 57432-86-7 3-(phenylthio)propionaldehyde diethyl acetal 
• 1126-80-3 (n-butylthio)benzene 
• 77331-04-5 2,2-bis(phenylthio)butanal 
• 100-68-5 methyl-phenyl-thioether 
• 14905-79-4 1-methylpropyl phenyl sulfide 

Relevant articles and documents

GAS PHASE SULFUR ANIONS: SYNTHESIS AND REACTIONS OF H2NS(1-) AND RELATED IONS

Many gas-phase anions react with carbonyl sulfide by sulfur atom transfer to form RS(1-) ions.The properties of H2NS(1-), formed in this way from H2N(1-) and OCS, are described.

Mesolysis Mechanisms of Aromatic Thioether Radical Anions Studied by Pulse Radiolysis and DFT Calculations

The mesolysis mechanisms for eight aromatic thioether radical anions (ArCH2SAr′?-) generated during radiolysis in 2-methyltetrahydrofuran were studied by spectroscopic measurements and DFT calculation. Seven of ArCH2SAr′s

Generation of alkoxycarbenium ion pools from thioacetals and applications to glycosylation chemistry

(Chemical Equation Presented) Alkoxycarbenium ions have been generated and accumulated as "cation pools" by the low-temperature electrochemical oxidation of α-phenylthioethers. Although an unsuccessful attempt to accumulate glycosyl cations was made, a one-pot method for electrochemical glycosylation, which involves anodic oxidation of thioglycosides to generate glycosyl cation equivalents followed by their reactions with glycosyl acceptors, has been developed.