111122-90-8

Basic information

• Product Name: 2-(2,4-Dimethoxy-phenyl)-2-phenyl-benzo[1,3]oxathiole
• Synonyms: 2-(2,4-Dimethoxy-phenyl)-2-phenyl-benzo[1,3]oxathiole
• CAS NO: 111122-90-8
• Molecular Weight: 350.438
• Mol File: 111122-90-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2,4-Dimethoxy-phenyl)-2-phenyl-benzo[1,3]oxathiole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4-Dimethoxy-phenyl)-2-phenyl-benzo[1,3]oxathiole(111122-90-8)
• EPA Substance Registry System: 2-(2,4-Dimethoxy-phenyl)-2-phenyl-benzo[1,3]oxathiole(111122-90-8)

Safety Data

• Hazardous Substances Data: 111122-90-8(Hazardous Substances Data)

Upstream product

• 111123-04-7 1,3-Dimethyl-2-(2-phenyl-benzo[1,3]oxathiol-2-yl)-1H-indole 
• 58948-35-9 2-phenyl-1,3-benzoxathiolium tetrafluoroborate 
• 151-10-0 1,3-Dimethoxybenzene 

Downstream Products

• 7697-46-3 phenyl(1H-pyrrol-2-yl)methanone 
• 15224-25-6 3-benzoylindole 
• 19012-01-2 3-benzoyl-1-methylindole 
• 3770-80-7 2,4,6-trimethoxybenzophenone 
• 60884-08-4 1-(2,4-dimethoxyphenyl)-2,2-dimethylpropan-1-one 
• 57600-76-7 4-chloro-2',4'-dimethoxybenzophenone 
• 111122-84-0 2,5-bisbenzoylpyrrole 
• 111122-95-3 2-<2-(2-Phenyl-1,3-benzoxathiolyl)>pyrrole 
• 111122-89-5 2-tert-Butyl-2-(2,4-dimethoxy-phenyl)-benzo[1,3]oxathiole 
• 111122-98-6 3-(2-Phenyl-benzo[1,3]oxathiol-2-yl)-1H-indole 
• 111123-02-5 1-Methyl-3-(2-phenyl-benzo[1,3]oxathiol-2-yl)-1H-indole 
• 111122-91-9 2-(4-Chloro-phenyl)-2-(2,4-dimethoxy-phenyl)-benzo[1,3]oxathiole 
• 111122-93-1 2-(2,4,6-Trimethoxyphenyl)-2-phenyl-1,3-benzoxathiole 
• 111122-96-4 2,5-Bis<2-(2-phenyl-1,3-benzoxathiolyl)>pyrrole 

Relevant articles and documents

2-Substituted 1,3-Benzoxathiolium Tetrafluoroborates as Useful Acylating Agents of Electron-Rich Aromatic and Heteroaromatic Compounds

2-Substituted 1,3-benzoxathiolium tetrafluoroborates were used for the two-step acylation of electron-rich aromatic and heteroaromatic compounds: 1,3-dimethoxybenzene, 1,3,5-trimethoxybenzene, pyrrole and indoles.In most of the cases intermediate 2,2-disubstituted 1,3-benzoxathioles were obtained in good to high yields (55-100percent) and subsequent hydrolysis of these with mercury(II) oxide and aqueous tetrafluoroboric acid (35percent) in tetrahydrofuran afforded the corresponding ketones in almost quantitative yields.