959625-33-3

Basic information

• Product Name: S-tert-Butyl 2-oxo-2-phenylethanethioate
• Synonyms: S-tert-Butyl 2-oxo-2-phenylethanethioate
• CAS NO: 959625-33-3
• Molecular Weight: 222.308
• Mol File: 959625-33-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: S-tert-Butyl 2-oxo-2-phenylethanethioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-tert-Butyl 2-oxo-2-phenylethanethioate(959625-33-3)
• EPA Substance Registry System: S-tert-Butyl 2-oxo-2-phenylethanethioate(959625-33-3)

Safety Data

• Hazardous Substances Data: 959625-33-3(Hazardous Substances Data)

Upstream product

• 611-73-4 Benzoylformic acid 
• 4358-87-6 (RS)-methyl mandelate 
• 15206-55-0 methyl 2-oxo-2-phenylacetate 
• 63599-51-9 S-tert-butyl hydroxy-phenyl-thioacetate 
• 25726-04-9 phenylglyoxylyl chloride 
• 75-66-1 2-methylpropan-2-thiol 

Downstream Products

• 63599-51-9 S-tert-butyl hydroxy-phenyl-thioacetate 
• 1034852-86-2 S-tert-butyl 2-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)-2-phenylethanethioate 

Relevant articles and documents

Non-Bonding 1,4-Sulphur-Oxygen Interaction Governs the Reactivity of α-Ketothioesters in Triphenylphosphine-Catalyzed Cyclization with Acetylenedicarboxylates

α-Ketothioesters undergo triphenylphosphine (PPh3)-catalyzed cyclization with acetylenedicarboxylate esters smoothly, in contrast to α-ketooxoesters which require more drastic conditions with the limited substrate scope. The reaction works well

ESR Studies on Carboxylic Esters. Part 13 - Electron Spin Resonance Spectroscopy and Molecular Orbital Calculations on the Radical Anions of 2-Oxo-carbothioate and 2-Oxo-carbodithioate Esters

Radical anions of alkyl α-oxocarbothioates and α-oxocarbodithioates are generated by in situ electroreduction.Their spin density distribution and configuration are discussed in terms of the ESR spectra and semi-empirical (McLachan-type and AM1) MO calculations. - Keywords: ESR α-Oxo-catbothioates α-Oxo-carbodithioates Radical anions MO calculations