94404-20-3

Basic information

• Product Name: (-)-(S_S)-(toluene-4-sulfinyl)-acetic acid tert-butyl ester
• Synonyms: (-)-(S_S)-(toluene-4-sulfinyl)-acetic acid tert-butyl ester
• CAS NO: 94404-20-3
• Molecular Weight: 254.35
• Mol File: 94404-20-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (-)-(S_S)-(toluene-4-sulfinyl)-acetic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-(S_S)-(toluene-4-sulfinyl)-acetic acid tert-butyl ester(94404-20-3)
• EPA Substance Registry System: (-)-(S_S)-(toluene-4-sulfinyl)-acetic acid tert-butyl ester(94404-20-3)

Safety Data

• Hazardous Substances Data: 94404-20-3(Hazardous Substances Data)

Upstream product

• 36304-27-5 tert-butyl 1-(p-tolylthio)acetate 
• 540-88-5 acetic acid tert-butyl ester 
• 1517-82-4 (1S,2R,5S)-2-isopropyl-5-methylcyclohexyl (R)-4-methylbenzenesulfinate 
• 1517-82-4 (-)-menthyl p-toluenesulfinate 
• 91796-57-5 4-Methyl-benzenesulfinic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester 

Downstream Products

• 1022349-69-4 C₂₃H₃₀O₅S 
• 1022349-68-3 C₂₃H₃₀O₅S 
• 151324-12-8 (1R,2R,αR,Rs)-(+)-(5,5-dimethyl-2-isopropenyl)-α-p-toluenesulfinylhexaneacetate 
• 155391-85-8 1,1-dimethylethyl (3S)-3-hydroxy-5-(phenylmethoxy)pentanoate 
• 131226-02-3 3-phenyl-2-(toluene-4-sulfinyl)-hexahydro-pyrazolo[1,2-a]pyridazin-1-one 
• 163460-81-9 tert-butyl (E)-[(S)-p-tolylsulfinyl]cinnamate 
• 132747-03-6 methyl (S)-(-)-p-toluenesulfinylacetate 
• 102340-68-1 (R)-(+)-methyl-α-(para-tolylsulfinyl) acetate 

Relevant articles and documents

ION PAIR CATALYSIS OF TUNGSTATE AND MOLYBDATE

D The present invention relates to ion pair catalysts (I) comprising the cationic bisguanidinium ligand (A) and diperoxomolybdate anion (B). The present invention also relates to ion pair catalysts (III) comprising the cationic bisguanidinium ligand (C) and peroxotungstate anion (D). It further relates to the use of the said catalysts in the manufacture of enantiomerically enriched sulfoxides.

3. Naphthopyranquinone Antibiotics: Novel Enantioselective Syntheses of Frenolicin B and Some of Its Stereoisomers

Two new enantioselective syntheses of the naphthopyranquinone antibiotic frenolicin B (1), of its enantiomer 2, and of its diastereoisomers 3 and 4 were accomplished using two different routes from optically active β-hydroxy esters (R)- and (S)-11 and 18.

Asymmetric Periodate Oxidation of Functionalized Sulfides Catalyzed by Bovine Serum Albumin

The asymmetric oxidation of the functionalized sulfides with sodium metaperiodate in the presence of a catalytic amount of bovine serum albumin (BSA) affords the corresponding sulfoxides with enantiomeric excess (ee) up to 69.3percent.The influence of the